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Post-ICU Ambulatory Care

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141. Non-Invasive Aortic Ambulatory Blood Pressure Monitoring for The Detection of Target Organ Damage in The Chinese Population

the maximum number of saved studies (100). Please remove one or more studies before adding more. Non-Invasive Aortic Ambulatory Blood Pressure Monitoring for The Detection of Target Organ Damage in The Chinese Population (SAFAR-China) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating (...) Non-Invasive Aortic Ambulatory Blood Pressure Monitoring for The Detection of Target Organ Damage in The Chinese Population Non-Invasive Aortic Ambulatory Blood Pressure Monitoring for The Detection of Target Organ Damage in The Chinese Population - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached

2017 Clinical Trials

142. Impact of the DROP Program on the DRP (Drug Related Problems) Related to Oral Anticancer Drugs in Ambulatory Patients With Risk Factors

of the market authorization. Adherence to the oral anticancer drug [ Time Frame: 6 months post-inclusion ] Adherence will be measured with the 8-item Morisky Medication Adherence Scale (MMAS-8; adherence will be defined as a score ≥7) and the rate of prescription renewal by the ambulatory pharmacy (adherence will be defined as a rate ≥80%). Number of imaging acts and nature of acts [ Time Frame: During the 6 months of follow-up ] To evaluate consumption of unscheduled ambulatory care related to DRP Number (...) of information sharing [ Time Frame: During the 9 months of follow-up ] To evaluate the involvement of primary care actors in the DROP program Patient's satisfaction for the DROP program [ Time Frame: At 9 months post-inclusion ] Satisfaction will be measured with a 10-point visual analog scale. Ambulatory care physician's and pharmacist's satisfactions with the DROP program [ Time Frame: At 9 months post-inclusion ] Satisfaction will be measured with a 10-point visual analog scale. Efficiency of the DROP

2017 Clinical Trials

143. Dexamethasone Administration To Improve Patient Recovery In Ambulatory Vaginal Prolapse Surgery: Is There A Role?

studies (100). Please remove one or more studies before adding more. Dexamethasone Administration To Improve Patient Recovery In Ambulatory Vaginal Prolapse Surgery: Is There A Role? The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov (...) Dexamethasone Administration To Improve Patient Recovery In Ambulatory Vaginal Prolapse Surgery: Is There A Role? Dexamethasone Administration To Improve Patient Recovery In Ambulatory Vaginal Prolapse Surgery: Is There A Role? - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved

2017 Clinical Trials

144. Feasibility of Ambulatory Hysterectomy

validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03290339 Recruitment Status : Recruiting First Posted : September 21, 2017 Last Update Posted : October 11, 2017 See Sponsor: University Hospital, Caen Collaborator: Amiens University Hospital (...) Feasibility of Ambulatory Hysterectomy Feasibility of Ambulatory Hysterectomy - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Feasibility of Ambulatory Hysterectomy (AMETHYST) The safety and scientific

2017 Clinical Trials

145. Type 2 Diabetes and Ambulatory Surgery Patients

maintenance intravascular fluids are avoided throughout the anesthesia and surgery unless specifically indicated for treatment. All patients will be awakened and extubated at the end of surgery and transferred to the post anesthesia recovery (PAR) area as appropriate. Capillary blood glucose will be measured after arrival in the PAR. The capillary glucose tests obtained in this study is part of established and standard care and will be paid for by the patient. Study Design Go to Layout table for study (...) Type 2 Diabetes and Ambulatory Surgery Patients Type 2 Diabetes and Ambulatory Surgery Patients - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Type 2 Diabetes and Ambulatory Surgery Patients (Diabetes

2017 Clinical Trials

146. Feasability of Ambulatory Appendicectomy

Patient Satisfaction [ Time Frame: 8 days post operative ] Patient Satisfaction will be assessed through a questionnaire number of overnight stays caused by the failures of ambulatory care [ Time Frame: 8 days post operative ] All hospitalization nights will be counted for patients in check up to day 8 in immediate postoperative re-admission rate at day 30 [ Time Frame: 30 days post operative ] The readmission rate will be defined as the percentage of patients rehospitalized at least once to 30 days (...) of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03186105 Recruitment Status : Recruiting First Posted : June 14, 2017 Last Update Posted : July 30, 2018 See Sponsor: Fondation Lenval Information provided by (Responsible Party): Fondation Lenval Study Details Study

2017 Clinical Trials

147. Management of Intraoperative Fluids in Ambulatory Surgery

in Ambulatory Surgery (MIFAS) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03193320 Recruitment Status : Not yet recruiting First Posted : June 20, 2017 Last Update Posted : November 27, 2018 See Sponsor: Policlinica (...) Management of Intraoperative Fluids in Ambulatory Surgery Management of Intraoperative Fluids in Ambulatory Surgery - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Management of Intraoperative Fluids

2017 Clinical Trials

148. Comparison of Ambulatory and Functional Improvement by Morning Walk

of Ambulatory and Functional Improvement by Morning Walk The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT03183856 Recruitment Status : Completed First Posted : June 12, 2017 Last Update Posted : May 30, 2018 Sponsor: Ulsan University Hospital Collaborator: Ministry of Health & Welfare, Korea Information (...) Comparison of Ambulatory and Functional Improvement by Morning Walk Comparison of Ambulatory and Functional Improvement by Morning Walk - Full Text View - ClinicalTrials.gov Hide glossary Glossary Study record managers: refer to the if submitting registration or results information. Search for terms x × Study Record Detail Saved Studies Save this study Warning You have reached the maximum number of saved studies (100). Please remove one or more studies before adding more. Comparison

2017 Clinical Trials

149. Avoiding Bacterial Contamination of Clean Catch Urine Cultures in Ambulatory Patients in the Emergency Department

studies (100). Please remove one or more studies before adding more. Avoiding Bacterial Contamination of Clean Catch Urine Cultures in Ambulatory Patients in the Emergency Department The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT03131609 Recruitment Status : Completed First Posted : April 27, 2017 (...) -soap wipe Sterile urine collection container and Castile-soap wipe given to patient to self-obtain a clean catch mid-stream urine specimen - Control group represents usual care in the Emergency Department. Other: Container Ambulatory patients in the Emergency Department who have a urine culture ordered by the physician receive one of four urine collection/hygiene options. Other Name: Standard container for urine collection Other: Castile-soap wipe Ambulatory patients in the Emergency Department who

2017 Clinical Trials

150. ACEI/ARB Study in Ambulatory and Day of Surgery Admission Patients

in Ambulatory and Day of Surgery Admission Patients (ACE/ARB) The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our for details. ClinicalTrials.gov Identifier: NCT03121092 Recruitment Status : Terminated (Due to difficulty with recruiting patients meeting the inclusion criteria the PI decided to retire this project.) First Posted : April 19, 2017 Last Update (...) of surgery. Drug: ACEI or ARB Angiotensin converting enzyme inhibitors (ACEI's) and Angiotensin receptor blockers (ARB's) - commonly used anti-hypertensive medications Outcome Measures Go to Primary Outcome Measures : Presence of moderate hypotension [ Time Frame: Through study completion, projected 2-3 years ] Presence of moderate hypotension (SBP<90 or a change of >30% from pre-induction baseline), in the intraoperative setting and in the post-anesthesia care unit Presence of severe hypotension [ Time

2017 Clinical Trials

151. Pain Medication After Ambulatory Surgery

of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. of clinical studies and talk to your health care provider before participating. Read our for details. ClinicalTrials.gov Identifier: NCT03135470 Recruitment Status : Recruiting First Posted : May 1, 2017 Last Update Posted : December 5, 2018 See Sponsor: Helsinki University Central Hospital Information provided by (Responsible Party): Noora Skants (...) , Helsinki University Central Hospital Study Details Study Description Go to Brief Summary: In Finland, there are no guidelines concerning post-operative pain medication of ambulatory surgery patients. There is a wide variety in drug prescription and medication practices of various doctors and clinics. To treat patients' pain safely, type of surgery, unique patient needs, risks, adverse effects and patient's capacity to follow instructions should be assessed during the few hour visit at the clinic

2017 Clinical Trials

152. Safety and efficacy of olesoxime in patients with type 2 or non-ambulatory type 3 spinal muscular atrophy: a randomised, double-blind, placebo-controlled phase 2 trial. (PubMed)

, phase 2 study was done in 22 neuromuscular care centres in Belgium, France, Germany, Italy, Netherlands, Poland, and the UK. Safety and efficacy of olesoxime were assessed in patients aged 3-25 years with genetically confirmed type 2 or non-ambulatory type 3 SMA. A centralised, computerised randomisation process allocated patients (2:1 with stratification by SMA type and centre) to receive olesoxime (10 mg/kg per day) in an oral liquid suspension or placebo for 24 months. Patients, investigators (...) Safety and efficacy of olesoxime in patients with type 2 or non-ambulatory type 3 spinal muscular atrophy: a randomised, double-blind, placebo-controlled phase 2 trial. Spinal muscular atrophy (SMA) is a progressive motor neuron disease causing loss of motor function and reduced life expectancy, for which limited treatment is available. We investigated the safety and efficacy of olesoxime in patients with type 2 or non-ambulatory type 3 SMA.This randomised, double-blind, placebo-controlled

2017 The Lancet. Neurology Controlled trial quality: predicted high

153. A Pain Education Intervention for Patients Undergoing Ambulatory Inguinal Hernia Repair: A Randomized Controlled Trial. (PubMed)

A Pain Education Intervention for Patients Undergoing Ambulatory Inguinal Hernia Repair: A Randomized Controlled Trial. Background Inguinal hernia repair is a common ambulatory surgery after which many patients experience moderate to severe post-operative pain. Limited research has examined the effect of education interventions to reduce pain after ambulatory surgery. Purpose This trial evaluated the effectiveness of an individualized Hernia Repair Education Intervention (HREI) for patients (...) following inguinal hernia repair. Method Pre-operatively, participants (N = 82) were randomized to either the intervention (HREI) or the usual care group. The HREI included written and verbal information regarding managing pain and two telephone support calls (before and after surgery). The primary outcome was WORST 24-h pain intensity on movement on post-operative day 2. Secondary outcomes included pain intensity at rest and movement, pain-related interference with activities, pain quality, analgesics

2017 The Canadian journal of nursing research = Revue canadienne de recherche en sciences infirmieres Controlled trial quality: predicted high

154. Safety and efficacy of olesoxime in patients with type 2 or non-ambulatory type 3 spinal muscular atrophy: a randomised, double-blind, placebo-controlled phase 2 trial. (PubMed)

, phase 2 study was done in 22 neuromuscular care centres in Belgium, France, Germany, Italy, Netherlands, Poland, and the UK. Safety and efficacy of olesoxime were assessed in patients aged 3-25 years with genetically confirmed type 2 or non-ambulatory type 3 SMA. A centralised, computerised randomisation process allocated patients (2:1 with stratification by SMA type and centre) to receive olesoxime (10 mg/kg per day) in an oral liquid suspension or placebo for 24 months. Patients, investigators (...) Safety and efficacy of olesoxime in patients with type 2 or non-ambulatory type 3 spinal muscular atrophy: a randomised, double-blind, placebo-controlled phase 2 trial. Spinal muscular atrophy (SMA) is a progressive motor neuron disease causing loss of motor function and reduced life expectancy, for which limited treatment is available. We investigated the safety and efficacy of olesoxime in patients with type 2 or non-ambulatory type 3 SMA.This randomised, double-blind, placebo-controlled

2017 Lancet Neurology Controlled trial quality: predicted high

155. Postoperative Sore Throat Prevention in Ambulatory Surgery: A Comparison between Preoperative Aspirin and Magnesium Sulfate Gargle - A Prospective, Randomized, Double-blind Study. (PubMed)

Postoperative Sore Throat Prevention in Ambulatory Surgery: A Comparison between Preoperative Aspirin and Magnesium Sulfate Gargle - A Prospective, Randomized, Double-blind Study. Postoperative sore throat (POST) frequently hampers the positive feedback of ambulatory surgery in spite of so many measures. This study was carried out to compare the efficacy of preoperative magnesium sulfate and aspirin gargle in preventing POST after ambulatory surgery.It was a prospective, randomized, and double (...) in magnesium group compared to aspirin group after the operation at 0, 2, 4 h after operation.It is evident that preoperative magnesium sulfate gargle significantly attenuated the incidence and severity of POST, especially in the early postoperative period, with no adverse effects in patients undergoing day care surgery under general anesthesia.

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2017 Anesthesia, essays and researches Controlled trial quality: uncertain

156. Perioperative Factors Affecting Ambulatory Outcomes Following Laparoscopic-Adjustable Gastric Banding (PubMed)

Perioperative Factors Affecting Ambulatory Outcomes Following Laparoscopic-Adjustable Gastric Banding Morbidly obese patients are traditionally hospitalised following bariatric surgery. However, laparoscopic-adjustable gastric banding (LAGB) is amenable for ambulatory care. We hypothesised that the majority of patients can receive an ambulatory LAGB and that both surgical and anaesthetic perioperative factors will significantly affect non-ambulatory LAGB outcomes.Medical records of 201 (...) ±10.3 kg m2-1. A total of 155 patients (77.1%; 95% confidence interval, 71%-83%; p<0.0001) were discharged home within 2-3 hours of surgery, whereas 36 stayed for 23 hours and 10 required hospital admission for 1-2 days. Increased surgical port numbers (p=0.007), ≥50% of total intraoperative fentanyl administered in the recovery room (post-anaesthesia care unit) for the treatment of postoperative pain (p=0.007) and a lack of prophylactic beta-blockade (p=0.001) were three factors associated with non

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2017 Turkish journal of anaesthesiology and reanimation

157. Recovery Profile After General Anaesthesia in Paediatric Ambulatory Surgeries: Desflurane Versus Propofol (PubMed)

, postoperative recovery profile, adverse events and comparative cost of anaesthetic agents were analysed.The mean heart rate in the desflurane group was significantly higher. There was no difference between the blood pressure, end tidal carbon dioxide, or oxygen saturation in the two groups. There was a trend towards faster awakening, spontaneous respiration and extubation, quicker time to achieve a fast track score >12 and shift out of the post-anaesthesia care unit in the desflurane group (...) Recovery Profile After General Anaesthesia in Paediatric Ambulatory Surgeries: Desflurane Versus Propofol Paediatric ambulatory surgeries warrant a speedy recovery of patients without compromising their safety. Short-acting agents such as propofol and desflurane help facilitate these objectives. In this prospective, randomised study we compared the recovery profile in paediatric patients undergoing ambulatory surgeries who received entropy guided general anaesthesia (GA) using desflurane

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2017 Turkish journal of anaesthesiology and reanimation Controlled trial quality: uncertain

158. Models of providing medical care to community-dwelling elderly with dementia in the ambulatory setting

Models of providing medical care to community-dwelling elderly with dementia in the ambulatory setting Print | PDF PROSPERO This information has been provided by the named contact for this review. CRD has accepted this information in good faith and registered the review in PROSPERO. CRD bears no responsibility or liability for the content of this registration record, any associated files or external websites. Email salutation (e.g. "Dr Smith" or "Joanne") for correspondence: Organisation web (...) stratified analysis (treatment pre-ischemia vs during vs post-ischemia). We will assess the effect of our decision to pool all reported scales for histological damage by re-running the analyses using only data from studies using the Jablonski scale. ">Sensitivity Example: For meta-analyses using the mean difference or risk ration as effect measure and containing at least 20 studies, we will produce funnel plots and assess publication bias using Egger’s regression test. ">Publication bias

2018 PROSPERO

159. The comparative effectiveness of ambulatory care warfarin management models

The comparative effectiveness of ambulatory care warfarin management models Print | PDF PROSPERO This information has been provided by the named contact for this review. CRD has accepted this information in good faith and registered the review in PROSPERO. CRD bears no responsibility or liability for the content of this registration record, any associated files or external websites. Email salutation (e.g. "Dr Smith" or "Joanne") for correspondence: Organisation web address: Timing and effect (...) stratified analysis (treatment pre-ischemia vs during vs post-ischemia). We will assess the effect of our decision to pool all reported scales for histological damage by re-running the analyses using only data from studies using the Jablonski scale. ">Sensitivity Example: For meta-analyses using the mean difference or risk ration as effect measure and containing at least 20 studies, we will produce funnel plots and assess publication bias using Egger’s regression test. ">Publication bias

2018 PROSPERO

160. Systematic review of socioeconomic inequalities in hospitalizations for ambulatory care sensitive conditions in economically developed countries

Systematic review of socioeconomic inequalities in hospitalizations for ambulatory care sensitive conditions in economically developed countries Print | PDF PROSPERO This information has been provided by the named contact for this review. CRD has accepted this information in good faith and registered the review in PROSPERO. CRD bears no responsibility or liability for the content of this registration record, any associated files or external websites. Email salutation (e.g. "Dr Smith" or "Joanne (...) of linear regression of time-to-treatment by performing stratified analysis (treatment pre-ischemia vs during vs post-ischemia). We will assess the effect of our decision to pool all reported scales for histological damage by re-running the analyses using only data from studies using the Jablonski scale. ">Sensitivity Example: For meta-analyses using the mean difference or risk ration as effect measure and containing at least 20 studies, we will produce funnel plots and assess publication bias using

2018 PROSPERO

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