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Dry Mouth

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121. Assess the Safety and Efficacy of CsA Ophthalmic Gel in Subjects With Dry Eye

Assess the Safety and Efficacy of CsA Ophthalmic Gel in Subjects With Dry Eye Assess the Safety and Efficacy of CsA Ophthalmic Gel in Subjects With Dry Eye - 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 (...) . Assess the Safety and Efficacy of CsA Ophthalmic Gel in Subjects With Dry Eye 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: NCT03676335 Recruitment Status : Recruiting First Posted : September 18, 2018 Last Update Posted

2018 Clinical Trials

122. Does Dry Needling Increase the Efficacy of Botulinum Toxin Injection in the Treatment of Poststroke Spasticity: A Randomized Controlled Study

Does Dry Needling Increase the Efficacy of Botulinum Toxin Injection in the Treatment of Poststroke Spasticity: A Randomized Controlled Study Dry Needling and Botulinum Toxin in the Management of Poststroke Spasticity - 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. Dry Needling and Botulinum Toxin in the Management of Poststroke Spasticity 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: NCT03747900 Recruitment Status : Completed First Posted : November 20, 2018 Last Update Posted : December 18, 2018

2018 Clinical Trials

123. Investigation of the Safety and Pharmacology of Dry Powder Inhalation of Treprostinil

Investigation of the Safety and Pharmacology of Dry Powder Inhalation of Treprostinil Investigation of the Safety and Pharmacology of Dry Powder Inhalation of Treprostinil - 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. Investigation of the Safety and Pharmacology of Dry Powder Inhalation of Treprostinil (INSPIRE) 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: NCT03399604 Recruitment Status : Recruiting First Posted : January

2018 Clinical Trials

124. Efficacy of Two Concentrations of Autologous Serum for the Treatment of Severe Dry Eye

Efficacy of Two Concentrations of Autologous Serum for the Treatment of Severe Dry Eye Efficacy of Two Concentrations of Autologous Serum for the Treatment of Severe Dry Eye - 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. Efficacy of Two Concentrations of Autologous Serum for the Treatment of Severe Dry Eye 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: NCT03436576 Recruitment Status : Enrolling by invitation First Posted : February 16, 2018 Last Update Posted : September 5, 2018 Sponsor: Pontificia

2018 Clinical Trials

125. Dietary Supplementation with a Combination of Lactoferrin, Fish Oil, and Enterococcus faecium WB2000 for Treating Dry Eye: A Rat Model and Human Clinical Study. (Abstract)

volunteers aged 22 to 59 years were randomized into combined dietary supplement (2 capsules/day; 20 participants) and placebo (vehicle; 19 participants) groups and treated once daily for 8 weeks. Rats received the combined dietary supplement components (10 or 50 mg/kg orally) or vehicle (2% DMSO), and dry eye was mechanically induced for 2 days. Tear production was measured in rats after dry eye was induced. Humans were assessed at baseline and weeks 4 and 8 post-supplementation based (...) Dietary Supplementation with a Combination of Lactoferrin, Fish Oil, and Enterococcus faecium WB2000 for Treating Dry Eye: A Rat Model and Human Clinical Study. To examine the effect of a combined dietary supplement containing fish oil, lactoferrin, zinc, vitamin C, lutein, vitamin E, γ-aminobutanoic acid, and Enterococcus faecium WB2000 on dry eye.A preliminary study in a rat model and a prospective, randomized, double-blind, placebo-controlled study in humans were conducted. Forty Japanese

2018 The ocular surface Controlled trial quality: uncertain

126. Antiocoagulation - oral

Antiocoagulation - oral Prodigy Toggle navigation Topics Specialities A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Allergies Cancer Cardiovascular Child health Drugs and devices Ear, nose and throat Endocrine and metabolic Eyes Gastroenterology Gastrointestinal Haematology Immunizations Infections and infestations Injuries Kidney disease and urology Men's health Mental health Musculoskeletal Neurological Oral health Palliative care Poisoning Pregnancy Preventative medicine Respiratory (...) Sexual health Skin and nail Women's health child health Anticoagulation - oral - Topic Menu Anticoagulation - oral: Summary There are five oral anticoagulants licensed for use in the UK: warfarin, apixaban, dabigatran, edoxaban and rivaroxaban. Apixaban, dabigatran, edoxaban and rivaroxaban are newer anticoagulants which may be prescribed instead of warfarin for people with non-valvular atrial fibrillation (NVAF): Apixaban, dabigatran, edoxaban and rivaroxaban have been approved by the National

2017 Prodigy

127. Clindamycin Exhibits No Statistical Difference in Preoperative Compared to Postoperative Administration For The Prevention of Dry Socket

Clindamycin Exhibits No Statistical Difference in Preoperative Compared to Postoperative Administration For The Prevention of Dry Socket UTCAT2622, Found CAT view, CRITICALLY APPRAISED TOPICs University: | | ORAL HEALTH EVIDENCE-BASED PRACTICE PROGRAM View the CAT / Title Clindamycin Exhibits No Statistical Difference in Preoperative Compared to Postoperative Administration For The Prevention of Dry Socket Clinical Question For dry socket prevention is it more efficacious to administer (...) , and limitations to the Kupfer study are the publication date and age of the study sample. Applicability For the prevention of dry socket with administration of Clindamycin, there is no significant difference in the gender and age of the patient or the location of the retained tooth. Clindamycin would be feasible in any clinical setting with the potential benefit of the prevention of dry socket following tooth extraction. Specialty/Discipline (General Dentistry) (Oral Surgery) Keywords Dry socket, clindamycin

2014 UTHSCSA Dental School CAT Library

128. Safety and efficacy of an intra-oral electrostimulator for the relief of dry mouth in patients with chronic graft versus host disease: Case series. Full Text available with Trip Pro

Safety and efficacy of an intra-oral electrostimulator for the relief of dry mouth in patients with chronic graft versus host disease: Case series. Patients with chronic graft-versus-host disease (cGVHD) often suffer from dry mouth and oral mucosal lesions. The primary objective of this study was to investigate the safety of an intra-oral electrostimulator (GenNarino) in symptomatic cGVHD patients. The secondary objective was to study the impact on the salivary gland involvement of cGVHD (...) lesions in areas in contact with the GenNarino during the study. However, only one of them had a change in the National Institutes of Health (NIH) score for oral cGVHD. The unstimulated and stimulated salivary flow rate increased in 4 out of the 5 patients included in this analysis. Symptoms of dry mouth and general oral comfort improved.This study suggests that GenNarino is safe in cGVHD patients with respect to oral tissues. Furthermore the use of GenNarino resulted in subjective and objective

2014 Medicina oral, patología oral y cirugía bucal Controlled trial quality: uncertain

129. The effect of cognitive appraisal for stressors on the oral health-related QOL of dry mouth patients Full Text available with Trip Pro

The effect of cognitive appraisal for stressors on the oral health-related QOL of dry mouth patients Dry mouth is very common symptom, and psychological factors have an influence on this symptom. Although the influence of emotional factor related to patients with oral dryness has been examined in previous studies, the cognitive factors have not been examined thus far.The purpose of this study was to examine the influence of cognitive factors on patients with oral dryness.The participants were (...) 106 patients complaining of oral dryness. They were required to complete a questionnaire measuring subjective oral dryness, oral-related QOL, cognition for stressors, and mood state.Correlational analyses revealed that OHIP-14 is significantly related to oral dryness, appraisal for effect, appraisal for threat, and commitment. These correlations were maintained even after controlling for the influence of depression and anxiety. Using oral dryness, appraisal for effect, appraisal for threat

2014 BioPsychoSocial medicine

130. Low level evidence suggests chlorhexidine gel (0.2%) is a better alternative to chlorhexidine rinse (0.12%) in preventing dry socket in third molar extractions when both are applied post-operatively.

Low level evidence suggests chlorhexidine gel (0.2%) is a better alternative to chlorhexidine rinse (0.12%) in preventing dry socket in third molar extractions when both are applied post-operatively. UTCAT2587, Found CAT view, CRITICALLY APPRAISED TOPICs University: | | ORAL HEALTH EVIDENCE-BASED PRACTICE PROGRAM View the CAT / Title Low Level Evidence Suggests Chlorhexidine Gel (0.2%) is a Better Alternative to Chlorhexidine Rinse (0.12%) in Preventing Dry Socket in Third Molar Extractions (...) When Both are Applied Post-Operatively Clinical Question Is chlorhexidine gel (0.2%) more effective than chlorhexidine rinse (0.12%) in preventing dry socket in third molar extractions? Clinical Bottom Line In the prevention of dry socket, treatment with chlorhexidine (gel and rinse) is better than placebo. There is minimal evidence to support that the gel has better effectiveness than the rinse. Both gel and rinse were post-operative applications. Best Evidence (you may view more info by clicking

2013 UTHSCSA Dental School CAT Library

131. Papules, Arthralgia, Dry Mouth and Dry Eyes: A Quiz. Full Text available with Trip Pro

Papules, Arthralgia, Dry Mouth and Dry Eyes: A Quiz. 22367265 2013 05 28 2013 01 10 1651-2057 93 1 2013 Jan Acta dermato-venereologica Acta Derm. Venereol. Papules, arthralgia, dry mouth and dry eyes: a quiz. Diagnosis: Multicentric reticulohistocytosis. 124-5 10.2340/00015555-1327 Jung Hee Dam HD Department of Dermatology, College of Medicine, The Catholic University of Korea 620-56, Jeonnong-dong, Dongdaemun-ku, Seoul, Korea. Kim Hei Sung HS Lee Jun Young JY Kim Hyung Ok HO Park Young Min YM

2013 Acta Dermato-Venereologica

132. Cold Sore - Guidelines for Prescribing Oral Antivirals

Cold Sore - Guidelines for Prescribing Oral Antivirals Cold Sore - Guidelines for Prescribing Oral Antivirals - medSask Home - College of Pharmacy and Nutrition - University of Saskatchewan Toggle Menu Search the U of S Search Cold Sore - Guidelines for Prescribing Oral Antivirals Commonly transmitted via saliva About 20 to 40% of patients who experience a primary herpes infection develop subsequent recurrent herpes infections caused by reactivation of HSV that remains latent in neural ganglion (...) , but still possible until lesions are fully healed and no longer producing exudate. Systemic symptoms are unusual and should cause suspicion for another condition. Orolabial herpes (cold sore) is diagnosed based on the presence of typical signs and symptoms (listed above). Rule out the following conditions that may present with similar signs / symptoms: - a bacterial infection most commonly caused by staphylococcus aureus. Can cause pustules to form around the mouth. It will be non-inflamed

2017 medSask

133. Blood and Clots Quizlet 1: Oral Contraceptives and Pulmonary Embolism

Blood and Clots Quizlet 1: Oral Contraceptives and Pulmonary Embolism Blood and Clots Quizlet 1: Oral Contraceptives and Pulmonary Embolism - CanadiEM Blood and Clots Quizlet 1: Oral Contraceptives and Pulmonary Embolism In , by Eric Tseng October 27, 2017 Hello Blood & Clots/CanadiEM community! Before we post our blog series on thrombosis and bleeding, we encourage you to test your initial knowledge by going through a few brief case scenarios. These cases were originally posted as part of our (...) needs assessment in Fall 2016, and you can find the answers after each question below. The Introduction to Blood and Clots post can be found . All the content from the Blood and Clots series can be found . Yours sincerely, The Blood & Clots Team * * * * * QUIZLET #1 Case Vignette Maria is a 27-year-old female university student with no past medical or surgical history, and has been taking an oral contraceptive pill for the past 8 years. She has never smoked. 2 days ago, she developed a new sharp

2017 CandiEM

134. CRACKCast E070 – Oral Medicine

CRACKCast E070 – Oral Medicine CRACKCast E070 - Oral Medicine - CanadiEM CRACKCast E070 – Oral Medicine In , by Adam Thomas April 10, 2017 This episode of CRACKCast covers Rosen’s Chapter 70, Oral Medicine. This chapter covers common tooth and mouth complaints that present to the ED and provides treatment and management tips to help with your next patient. Shownotes – Rosen’s in Perspective The oral cavity and associated facial structures, AKA stomatognathic system, is made up of the: Mandible (...) causes of oral ulcerations: Hand-foot-mouth / Herpetic stomatitis/ HIV / Syphilis / TB / Wegner’s / Scleroderma / Lupus / to name a few Symptomatic care Saline and Hydrogen peroxide rinses Mix of Benzocaine and diphenhydramine gel Rx for steroid – antibiotic ointments (Kenalog or orabase) F/U with GP to ensure resolution WiseCracks Case 1: Spot Diagnosis! 32yo male with obvious right sided deep space neck infection and chest pain, SOB and severe septic shock. Remember: Deep fascial layers of neck

2017 CandiEM

135. The Oral Management of Oncology Patients Requiring Radiotherapy, Chemotherapy and / or Bone Marrow Transplantation

be undertaken to stabilise periodontal disease. 2.1.8. Dental caries: Where possible carious teeth should be definitively restored or stabilised with appropriate restorations. 2.1.9. Removal of trauma: All sharp teeth and restorations are suitably adjusted and polished. 2.1.10. Impressions: Impressions of the mouth are taken for study casts to construct applicator trays and, where appropriate, for intra-oral radiation stents and obturator planning. 2.1.11. Dentures / obturators: The patient is counselled (...) Infections: Children and adults receiving bone marrow transplants often receive aciclovir as a prophylaxis if there is a high risk of viral infections. This is usually prescribed by the oncology team (Sanderr et al., 2015) (Ullmann et al., 2016). 2.2.6. Fungal Infections: Antifungal medication is used following detection of oral candida (Pappas et al., 2016). For children, this may be used routinely as a prophylaxis in some cancer centres. 2.2.7. Mucositis: Regular assessment of the mouth should

2018 British Society for Disability and Oral Health

136. Chlorhexidine gels and rinses reduce dry socket after third molar extraction

Chlorhexidine gels and rinses reduce dry socket after third molar extraction Chlorhexidine gels and rinses reduce dry socket after third molar extraction - National Elf Service Search National Elf Service Search National Elf Service » » » » Chlorhexidine gels and rinses reduce dry socket after third molar extraction Mar 13 2017 Posted by Dry socket (alveolar osteitis) is a common post-operative complication of permanent tooth extraction. Incidence of alveolar osteitis (AO) has been reported (...) . The primary outcome was incidence of AO and efficacy summaries using risk ratios (RR), preventive fraction and number needed to treat (NNT). Meta-analysis of binary data was conducted using a fixed-effects model. Result s 18 RCTs (16 parallel-group and 2 split-mouth) were included There were 2,824 third molar extractions (1,458 in experimental group and 1,366 in control group). 10 studies involved rinses, 4 using 0.2% concentration others 0.12%. 10 studies used gels, most using 0.2% concentration, 1 using

2017 The Dental Elf

137. Changes in bacterial number at different sites of oral cavity during perioperative oral care management in gastrointestinal cancer patients: preliminary study Full Text available with Trip Pro

days after the operation in patients who underwent open surgery. Furthermore, the dry mouth index level was higher in the open surgery group when compared to the laparoscopic surgery group on postoperative days 2 and 7.Even with regular oral health care, bacterial numbers remained high in the upper incisor tooth gingiva in gastrointestinal cancer patients who received open surgery. Additional procedures are likely needed to effectively reduce the number of bacteria in the gingival area associated (...) , Takarazuka Municipal Hospital, from 2015 to 2017 (n=71; 42 laparoscopic surgery, 29 open surgery) to determine changes in bacterial numbers at different sites of the oral cavity (tongue dorsum, gingiva of upper anterior teeth, palatoglossal arch), as well as mouth dryness and tongue coating indices. Specifically, patients received professional tooth cleaning (PTC), scaling, tongue cleaning, and self-care instruction regarding tooth brushing from a dental hygienist a day before the operation. Professional

2018 Journal of Applied Oral Science

138. Study to Evaluate the Efficacy and Safety of Tezepelumab in Reducing Oral Corticosteroid Use in Adults With Oral Corticosteroid Dependent Asthma

Study to Evaluate the Efficacy and Safety of Tezepelumab in Reducing Oral Corticosteroid Use in Adults With Oral Corticosteroid Dependent Asthma Study to Evaluate the Efficacy and Safety of Tezepelumab in Reducing Oral Corticosteroid Use in Adults With Oral Corticosteroid Dependent 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. Study to Evaluate the Efficacy and Safety of Tezepelumab in Reducing Oral Corticosteroid Use in Adults With Oral Corticosteroid Dependent Asthma (SOURCE) 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

2018 Clinical Trials

139. Bioequivalence Study of Ibuprofen D, Oral Suspension, 200 mg/5ml and Nurofen®, Oral Suspension 100 mg/5 ml in Healthy Volunteers Under Fasting Conditions

Bioequivalence Study of Ibuprofen D, Oral Suspension, 200 mg/5ml and Nurofen®, Oral Suspension 100 mg/5 ml in Healthy Volunteers Under Fasting Conditions Bioequivalence Study of Ibuprofen D, Oral Suspension, 200 mg/5ml and Nurofen®, Oral Suspension 100 mg/5 ml in Healthy Volunteers Under Fasting Conditions - 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. Bioequivalence Study of Ibuprofen D, Oral Suspension, 200 mg/5ml and Nurofen®, Oral Suspension 100 mg/5 ml in Healthy Volunteers Under Fasting Conditions 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

2018 Clinical Trials

140. Bioequivalence Study of Clavamox, Powder for Oral Suspension, 400 mg + 57 mg / 5 ml (Pharmtechnology LLC, Belarus), and Augmentin®, Powder for Oral Suspension, 400 mg + 57 mg / 5 ml (GlaxoSmithKline Trading CJSC, Russia), in Healthy Volunteers Under Fast

Bioequivalence Study of Clavamox, Powder for Oral Suspension, 400 mg + 57 mg / 5 ml (Pharmtechnology LLC, Belarus), and Augmentin®, Powder for Oral Suspension, 400 mg + 57 mg / 5 ml (GlaxoSmithKline Trading CJSC, Russia), in Healthy Volunteers Under Fast Bioequivalence Study of Clavamox, Powder for Oral Suspension, 400 mg + 57 mg / 5 ml (Pharmtechnology LLC, Belarus), and Augmentin®, Powder for Oral Suspension, 400 mg + 57 mg / 5 ml (GlaxoSmithKline Trading CJSC, Russia), in Healthy Volunteers (...) Under Fasting Conditions - 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. Bioequivalence Study of Clavamox, Powder for Oral Suspension, 400 mg + 57 mg / 5 ml (Pharmtechnology LLC, Belarus), and Augmentin®, Powder

2018 Clinical Trials

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