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Ice Pack Test

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1. Ice Pack Test

Ice Pack Test Ice Pack Test Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Ice Pack Test Ice Pack Test Aka: Ice Pack Test II (...) : Related links to external sites (from Bing) These images are a random sampling from a Bing search on the term "Ice Pack Test." Click on the image (or right click) to open the source website in a new browser window. Related Studies (from Trip Database) Related Topics in Examination About FPnotebook.com is a rapid access, point-of-care medical reference for primary care and emergency clinicians. Started in 1995, this collection now contains 6656 interlinked topic pages divided into a tree of 31

2018 FP Notebook

2. Cryotherapy Machines versus Ice Packs for the Post-Operative Management of Anterior Cruciate Ligament Replacement Surgery or Total Knee Arthroplasty: Clinical Evidence and Guidelines

Cryotherapy Machines versus Ice Packs for the Post-Operative Management of Anterior Cruciate Ligament Replacement Surgery or Total Knee Arthroplasty: Clinical Evidence and Guidelines Disclaimer: The Rapid Response Service is an information service for those involved in planning and providing health care in Canada. Rapid responses are based on a limited literature search and are not comprehensive, systematic reviews. The intent is to provide a list of sources of the best evidence on the topic (...) by the owners’ own terms and conditions. TITLE: Cryotherapy Machines versus Ice Packs for the Post-Operative Management of Anterior Cruciate Ligament Replacement Surgery or Total Knee Arthroplasty: Clinical Evidence and Guidelines DATE: 28 November 2012 RESEARCH QUESTIONS 1. What is the clinical evidence for the use of cyrotherapy machines versus ice packs for the post-operative management of anterior cruciate ligament replacement surgery or total knee arthroplasty? 2. What are the evidence-based guidelines

2013 Canadian Agency for Drugs and Technologies in Health - Rapid Review

3. Comparison of Ice Packs Application and Relaxation Therapy in Pain Reduction during Chest Tube Removal Following Cardiac Surgery. (PubMed)

Comparison of Ice Packs Application and Relaxation Therapy in Pain Reduction during Chest Tube Removal Following Cardiac Surgery. Usually the chest tube removal (CTR) has been described as one of the worst experiences by patients in the intensive care unit.This study aimed to compare the effects of cold therapy and relaxation on pain of CTR among the patients undergoes coronary artery bypass graft surgery.This single-blinded clinical trial was done on 80 post-cardiac surgery patients (...) in the heart hospital of Sari-Iran. The patients were assigned to three randomized groups that included cold therapy, relaxation, and control groups. Data analysis was done by T-test, Chi-square, generalized estimating equations and repeated measures analysis variance tests.The groups had no significant differences in pain intensity before CTR (P = 0.84), but immediately after CTR there was a significant difference between the treatment (cold application and relaxation groups) and control groups (P = 0.001

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2014 North American journal of medical sciences

4. Ice Packs Reduce Postoperative Midline Incision Pain and Narcotic Use: A Randomized Controlled Trial. (PubMed)

Ice Packs Reduce Postoperative Midline Incision Pain and Narcotic Use: A Randomized Controlled Trial. Postoperative pain is an unavoidable consequence of open abdominal surgery. Although cryotherapy, the application of ice to a surgical wound site, has been shown to be effective in reducing postoperative pain in orthopaedic, gynecologic, and hernia operations, it has not been assessed in patients who undergo major open abdominal operations. We hypothesized that patients who receive cryotherapy (...) by Student's t-test or Mann-Whitney U test for parametric and nonparametric data, respectively.There were 55 patients randomized: 28 to the control group and 27 to the cryotherapy group. For the primary measure, mean postoperative pain score on postoperative days (PODs) 1 and 3 after surgery was significantly lower between the control and cryotherapy groups on the visual analog pain scale (p < 0.005). Narcotic use was decreased in the cryotherapy group on POD 1 by 3.9 morphine equivalents (p = 0.008

2014 Journal of the American College of Surgeons.

5. Ice Pack Test

Ice Pack Test Ice Pack Test Toggle navigation Brain Head & Neck Chest Endocrine Abdomen Musculoskeletal Skin Infectious Disease Hematology & Oncology Cohorts Diagnostics Emergency Findings Procedures Prevention & Management Pharmacy Resuscitation Trauma Emergency Procedures Ultrasound Cardiovascular Emergencies Lung Emergencies Infectious Disease Pediatrics Neurologic Emergencies Skin Exposure Miscellaneous Abuse Cancer Administration 4 Ice Pack Test Ice Pack Test Aka: Ice Pack Test II (...) : Related links to external sites (from Bing) These images are a random sampling from a Bing search on the term "Ice Pack Test." Click on the image (or right click) to open the source website in a new browser window. Related Studies (from Trip Database) Related Topics in Examination About FPnotebook.com is a rapid access, point-of-care medical reference for primary care and emergency clinicians. Started in 1995, this collection now contains 6656 interlinked topic pages divided into a tree of 31

2015 FP Notebook

6. ICS Tracheostomy Standards (2014)

ICS Tracheostomy Standards (2014) TRACHEOSTOMY CARE INTENSIVE CARE SOCIETY STANDARDS © 2014 1 Standards for the care of adult patients with a temporary Tracheostomy; STANDARDS AND GUIDELINES Neither the Intensive Care Society nor the authors accept any responsibility for any loss of or damage arising from actions or decisions based on the information contained within this publication. Ultimate responsibility for the treatment of patients and interpretation of the published material lies (...) with the medical practitioner. The opinions expressed are those of the authors and the inclusion in this publication of material relating to a particular product or method does not amount to an endorsement of its value, quality, or the claims made by its manufacturer. Prepared on behalf of the Council of the Intensive Care Society by: Andrew Bodenham (Chair) Dominic Bell Steve Bonner Fiona Branch Deborah Dawson Paul Morgan Brendan McGrath Simon Mackenzie Ratified by ICS Council: Review date July 2018

2014 Intensive Care Society

7. The effect of cool water pack preparation on vaccine vial temperatures in refrigerators (PubMed)

The effect of cool water pack preparation on vaccine vial temperatures in refrigerators Cool water packs are a useful alternative to ice packs for preventing unintentional freezing of vaccines during outreach in some situations. Current guidelines recommend the use of a separate refrigerator for cooling water packs from ambient temperatures to prevent possible heat degradation of adjacent vaccine vials. To investigate whether this additional equipment is necessary, we measured the temperatures (...) that vaccine vials were exposed to when warm water packs were placed next to vials in a refrigerator. We then calculated the effect of repeated vial exposure to those temperatures on vaccine vial monitor status to estimate the impact to the vaccine. Vials were tested in a variety of configurations, varying the number and locations of vials and water packs in the refrigerator. The calculated average percentage life lost during a month of repeated warming ranged from 20.0% to 30.3% for a category 2 (least

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2018 Vaccine

8. Synthesis of Silica Microspheres—Inspired by the Formation of Ice Crystals—With High Homogeneous Particle Sizes and Their Applications in Photonic Crystals (PubMed)

to improve the synthesis rate of SMs, gaining inspiration from the formation mechanism of ice crystals. SMs with uniform particle sizes (polydispersity index less than 0.05) and good spherical features were fabricated through homogeneous nucleation. The mathematical relationship between particle sizes of SMs and reactant concentrations is further fitted. High accuracy of the regression equation is verified by an F-test and verification experiment. Highly ordered PCs (the stacking fault is about 1.5 (...) Synthesis of Silica Microspheres—Inspired by the Formation of Ice Crystals—With High Homogeneous Particle Sizes and Their Applications in Photonic Crystals Silica microspheres (SMs) must possess the performances of desirable monodispersity, narrow particle size distribution, and high sphericity for preparing photonic crystals (PCs) and other materials such as microspheres reference material, etc. We have adopted the techniques of increasing reactant concentration and raising the temperature

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2018 Materials

9. Strategies to link people with undiagnosed HIV infection to HIV testing, care, and prevention services

for conditions that indicated risk for or actual HIV infection – some of which could have been prevented if diagnosed with HIV earlier (12). Some researchers have suggested that there is a need for alternative provider-initiated targeted HIV testing strategies to those based on risk behaviours (13). Indicator Conditions (ICs) are conditions that tend to affect HIV-infected individuals more frequently, either because they are facilitated by immune deficiency, or they share modes of transmission (14). Many (...) researchers believe that offering HIV testing based on the presence of ICs has the potential to increase HIV testing and reduce stigma, as it removes the need for behavioural risk assessment (13). Using this strategy may also provide a means to prevent missed opportunities for HIV diagnosis. For example, a retrospective case-control study conducted in six general practices in Amsterdam found that 58.8% of new HIV cases had exhibited an HIV IC (most commonly syphilis and gonorrhea), compared with 7.4

2019 Ontario HIV Treatment Network

10. Intraoperative ice pack application for uvulopalatoplasty pain reduction: A randomized controlled trial. (PubMed)

assessed. T test and Mann-Whitney statistical analyses, as well as routine descriptive statistics, were conducted.Eighteen subjects were recruited. Patients that received intraoperative cold packs experienced a statistically significant change in VAS average pain [3.4 ± 1.1 cm (p = 0.00001)] when compared with patients receiving room temperature packs. No difference in return to work (p = 0.16) and return to normal diet (p = 0.12) was identified.Intraoperative ice pack administration results (...) Intraoperative ice pack application for uvulopalatoplasty pain reduction: A randomized controlled trial. Pain after uvulopalatoplasty continues to cause patients significant morbidity, especially from the tonsillectomy portion. The literature describes multiple techniques to reduce post-tonsillectomy pain, none being definitive. The purpose of this study was to evaluate the effect of intraoperative ice pack application on post-uvulopalatoplasty pain.Single-blinded, randomized controlled

2013 Laryngoscope

11. The Collaborative Assessment, OTCA12, on “C-reactive protein point-of-care testing (CRP POCT) to guide antibiotic prescribing in primary care settings for acute respiratory tract infections (RTIs)

The Collaborative Assessment, OTCA12, on “C-reactive protein point-of-care testing (CRP POCT) to guide antibiotic prescribing in primary care settings for acute respiratory tract infections (RTIs) Dec2015 © EUnetHTA, 2015. Reproduction is authorised provided EUnetHTA is explicitly acknowledged 1 EUnetHTA Joint Action 3 WP4 Version 1.4, +31 January 2019] Rapid assessment of other technologies using the HTA Core Model ® for Rapid Relative Effectiveness Assessment C-REACTIVE PROTEIN POINT-OF-CARE (...) TESTING (CRP POCT) TO GUIDE ANTIBIOTIC PRESCRIBING IN PRIMARY CARE SETTINGS FOR ACUTE RESPIRATORY TRACT INFECTIONS (RTIS) Project ID: OTCA012 C-reactive protein point-of-care testing to guide antibiotic prescribing for acute respiratory tract infections in primary care EUnetHTA Joint Action 3 WP4 2 DOCUMENT HISTORY AND CONTRIBUTORS Version Date Description V1.0 26/10/2018 First draft. V1.1 03/12/2018 Input from co-author has been processed. V1.2 03/12/2018 Input from dedicated reviewers has been

2019 EUnetHTA

12. Integrated Primary Care for Chronic Lung Disease: PACK Brazil

Integrated Primary Care for Chronic Lung Disease: PACK Brazil Integrated Primary Care for Chronic Lung Disease: PACK Brazil - 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. Integrated Primary Care (...) for Chronic Lung Disease: PACK Brazil (PACKBrazilR) 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: NCT02786030 Recruitment Status : Recruiting First Posted : May 30, 2016 Last Update Posted : April 27, 2018 See Sponsor

2016 Clinical Trials

13. TRIple in Asthma hiGh strenGth vErsus Ics/Laba hs and tiotRopium (TRIGGER)

old Uncontrolled asthma with double therapy only on high doses of Inhaled CorticoSteroid (ICS) in combination with Long-Acting Beta2 Agonist (LABA) with ACQ-7 (Asthma Control Questionnaire) ≥1.5 Pre-bronchodilator FEV1 <80% of the predicted normal value Positive reversibility test At least 1 documented asthma exacerbation in the previous year Exclusion Criteria: Pregnant or lactating women Diagnosis of Chronic Obstructive Pulmonary Disease (COPD) Patients with any asthma exacerbation (...) or respiratory tract infection in the 4 weeks prior screening Current smoker or ex-smoker (>= 10 packs year) Any change in dose, schedule or formulation of ICS + LABA combination in the 4 weeks prior screening Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number

2016 Clinical Trials

14. TRIple in asthMA With uncontRolled pAtient on Medium streNgth of ICS + LABA

40 years old Uncontrolled asthma with double therapy only on medium doses of Inhaled CorticoSteroid (ICS) in combination with Long-acting beta2 Agonist (LABA) with ACQ-7 (Asthma Control Questionnaire) ≥1.5 Pre-bronchodilator FEV1 <80% of the predicted normal value Positive reversibility test At least 1 documented asthma exacerbation in the previous year Exclusion Criteria: Pregnant or lactating women Diagnosis of Chronic Obstructive Pulmonary Disease (COPD) Patients with any asthma exacerbation (...) or respiratory tract infection in the 4 weeks prior screening Current or ex-smokers (>= 10 packs year) Any change in dose, schedule or formulation of ICS + LABA combination in the 4 weeks prior screening Contacts and Locations Go to Information from the National Library of Medicine To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor. Please refer to this study by its ClinicalTrials.gov identifier (NCT number

2016 Clinical Trials

15. Updated Molecular Testing Guideline for the Selection of Lung Cancer Patients for Treatment With Targeted Tyrosine Kinase Inhibitors

Updated Molecular Testing Guideline for the Selection of Lung Cancer Patients for Treatment With Targeted Tyrosine Kinase Inhibitors CAP Laboratory Improvement Programs Updated Molecular Testing Guideline for the Selection of Lung Cancer Patients for Treatment With Targeted Tyrosine Kinase Inhibitors GuidelineFromtheCollegeofAmericanPathologists,theInternationalAssociation for the Study of Lung Cancer, and the Association for Molecular Pathology Neal I. Lindeman, MD; Philip T. Cagle, MD; Dara L (...) guideline was published by the College of American Pathologists, the InternationalAssociationfortheStudyofLungCancer,and the Association for Molecular Pathology to set standards forthe molecularanalysisof lung cancers to guide treatment decisions with targeted inhibitors. New evi- dencehas promptedanevaluationofadditionallaboratory technologies, targetable genes, patient populations, and tumor types for testing. Objective.—To systematically review and update the 2013 guideline to affirm its validity

2017 College of American Pathologists

16. Exhaled NO Based Treatment of Chronic Obstructive Pulmonary Disease (COPD), ICS/LABA Versus LAMA

Exhaled NO Based Treatment of Chronic Obstructive Pulmonary Disease (COPD), ICS/LABA Versus LAMA Exhaled NO Based Treatment of Chronic Obstructive Pulmonary Disease (COPD), ICS/LABA Versus LAMA - 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. Exhaled NO Based Treatment of Chronic Obstructive Pulmonary Disease (COPD), ICS/LABA Versus LAMA 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: NCT02546349 Recruitment Status : Unknown Verified September 2015 by Taipei Veterans General Hospital, Taiwan. Recruitment

2015 Clinical Trials

17. A Study to Compare the Efficacy of Fluticasone Furoate/Vilanterol Inhalation Powder With Usual Inhaled Corticosteroids (ICS)/Long Acting Beta Agonists (LABA) in Persistent Asthma

A Study to Compare the Efficacy of Fluticasone Furoate/Vilanterol Inhalation Powder With Usual Inhaled Corticosteroids (ICS)/Long Acting Beta Agonists (LABA) in Persistent Asthma A Study to Compare the Efficacy of Fluticasone Furoate/Vilanterol Inhalation Powder With Usual Inhaled Corticosteroids (ICS)/Long Acting Beta Agonists (LABA) in Persistent Asthma - 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. A Study to Compare the Efficacy of Fluticasone Furoate/Vilanterol Inhalation Powder With Usual Inhaled Corticosteroids (ICS)/Long Acting Beta Agonists (LABA) in Persistent Asthma The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing

2015 Clinical Trials

18. MCID in 30 STS Test After PR in COPD Patients

MCID in 30 STS Test After PR in COPD Patients MCID in 30 STS Test After PR in COPD 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. MCID in 30 STS Test After PR in COPD Patients (COPD) The safety (...) Party): elisabetta zampogna, Maugeri Foundation Study Details Study Description Go to Brief Summary: The sit-to-stand test (STST) is a feasible alternative for measuring peripheral muscle strength of the lower limbs. Our aim was to evaluate, in Chronic Obstructive Pulmonary Disease (COPD) patients, the minimal clinically important difference (MCID) of 30-second STST (30-STST) after pulmonary rehabilitation (PR). Stable COPD inpatients undergoing 30-STST and 6-minute walk test (6MWT) before and after

2018 Clinical Trials

19. A Study to Test if a Third Dose of the Vaccine is Safe in Current and Former Smokers Aged 40 to 80 Years Old and to Gather Information on the Immune Response Following the Third Dose of the Vaccine

A Study to Test if a Third Dose of the Vaccine is Safe in Current and Former Smokers Aged 40 to 80 Years Old and to Gather Information on the Immune Response Following the Third Dose of the Vaccine A Study to Test if a Third Dose of the Vaccine is Safe in Current and Former Smokers Aged 40 to 80 Years Old and to Gather Information on the Immune Response Following the Third Dose of the Vaccine - 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. A Study to Test if a Third Dose of the Vaccine is Safe in Current and Former Smokers Aged 40 to 80 Years Old and to Gather Information on the Immune Response Following the Third Dose of the Vaccine The safety and scientific validity of this study is the responsibility

2018 Clinical Trials

20. ICS/LABA Combination With Integrated Dose Counter and Smartphone APP to Improve Asthma Control

ICS/LABA Combination With Integrated Dose Counter and Smartphone APP to Improve Asthma Control ICS/LABA Combination With Integrated Dose Counter and Smartphone APP to Improve Asthma Control - 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. ICS/LABA Combination With Integrated Dose Counter and Smartphone APP to Improve Asthma Control 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: NCT02556073 Recruitment Status : Unknown Verified September 2015 by Taipei Veterans General Hospital, Taiwan. Recruitment

2014 Clinical Trials

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