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15881. Cardiac Rehabilitation in Patients With Refractory Angina

Cardiac Rehabilitation in Patients With Refractory Angina Cardiac Rehabilitation in Patients With Refractory Angina - 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. Cardiac Rehabilitation in Patients (...) ; Detection of ischemic episodes and arrhythmias identified during the Rehabilitation sessions through external cardiac monitoring (telemetry); Evaluate the quality of life assessment through the SF-36 questionnaire, Canadian Cardiovascular Society, the number of symptomatic episodes of ischemia, daily sublingual nitrate intake. Condition or disease Intervention/treatment Phase Refractory Angina Behavioral: Cardiac Rehabilitation Not Applicable Detailed Description: After signing the informed consent form

2017 Clinical Trials

15882. Effectiveness of Proprioceptive Exercise in Neck Pain

links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: Control group Follow the usual treatment and perform the exercises of cervical mobility before a mirror. Other: Mobility exercises Usual treatment and exercises of cervical mobility before a mirror. Experimental: Experimental group The same procedure is followed by substituting proprioceptive exercises for craniocervical sensorimotor control with a laser (...) Effectiveness of Proprioceptive Exercise in Neck Pain Effectiveness of Proprioceptive Exercise in Neck Pain - 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. Effectiveness of Proprioceptive Exercise in Neck

2017 Clinical Trials

15883. Tourniquets Type Combat Application Tourniquet: Proximal or Distal Location, Simple or Staggered on Upper and Lower Limb

or Distal Location, Simple or Staggered. Study to Upper and Lower Limbs Actual Study Start Date : July 31, 2017 Actual Primary Completion Date : October 23, 2017 Actual Study Completion Date : October 23, 2017 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: Proximal single upper limb Laying a single tourniquet on the root of the upper limb Device: Proximal single upper limb Measurement of pain (...) will be evaluated by the loss of the radial doppler flux for the tourniquets placed on the upper limb and in the tibial anterior to the lower limb by the loss of the pulse oximetry pulse and the collection of the signs described by the volunteers (pain, Paresthesia, cold sensation). Condition or disease Intervention/treatment Phase Hemorrhage Device: Proximal single upper limb Device: Proximal staggered upper limb Device: Distal single upper limb Device: Distal staggered upper limb Device: Proximal single lower

2017 Clinical Trials

15884. Optimal Remifentanil Concentration and Thyroidectomy

topics: available for: Arms and Interventions Go to Arm Intervention/treatment Experimental: remifentanil After skin suture, a predetermined Effect site remifentanil concentration will be achieved. Starting from 1.5 ng/ml in the first patient and increased or decreased by 0.2 ng/ml intervals based on the previous patient response: up if cough present, down otherwise ("Dixon's up and down" method). Other: Remifentanil Effect site concentration After skin suture, a predetermined Effect site (...) Optimal Remifentanil Concentration and Thyroidectomy Optimal Remifentanil Concentration and Thyroidectomy - 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. Optimal Remifentanil Concentration and Thyroidectomy

2017 Clinical Trials

15885. Clinical Trial to Evaluate the Efficacy and Safety of 'GLA5PR GLARS-NF1 Tab.' in Peripheral Neuropathic Pain

Posted : March 19, 2019 Sponsor: Daewon Pharmaceutical Co., Ltd. Information provided by (Responsible Party): Daewon Pharmaceutical Co., Ltd. Study Details Study Description Go to Brief Summary: A multi-center, randomized, double-blind, parallel, active-controlled phase III clinical trial to evaluate the efficacy and safety of 'GLA5PR GLARS-NF1 Tab.' and 'Pregabalin' in peripheral neuropathic pain Condition or disease Intervention/treatment Phase Pain of Mononeuropathy Drug: GLA5PR GLARS-NF1 Drug (...) GLARS-NF1 Tab.' and 'Pregabalin' in Peripheral Neuropathic Pain Actual Study Start Date : April 11, 2016 Actual Primary Completion Date : January 8, 2019 Actual Study Completion Date : January 8, 2019 Resource links provided by the National Library of Medicine related topics: related topics: available for: resources: Arms and Interventions Go to Arm Intervention/treatment Experimental: GLA5PR GLARS-NF1 & Pregabalin placebo GLA5PR GLARS-NF1 150mg, 300mg tablet by mouth, every after dinner for about 3

2017 Clinical Trials

15886. Remifentanil and Desflurane Inhalational Anesthesia in Bariatric Surgeries

to the first painkiller required will be registered Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Estimated Enrollment : 120 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: Triple (Participant, Care Provider, Outcomes Assessor) Primary Purpose: Treatment Official Title: The Recovery Profile of Different Doses of Remifentanil After Desflurane Inhalational Anesthesia for Bariatric Surgeries: Two Centers Controlled (...) Prospective Study Estimated Study Start Date : July 20, 2017 Estimated Primary Completion Date : November 1, 2017 Estimated Study Completion Date : November 1, 2017 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Placebo Comparator: Group 1(Normal saline) Patients who will receive placebo (one ml normal saline). The drug will be given after closure of desflurane at an exhaled MAC of 0.3. Drug: Normal Saline

2017 Clinical Trials

15887. Sleep Apnea, Cardiovascular and Exercise Study

the Effects of Exercise on Vascular Function in Obstructive Sleep Apnea Actual Study Start Date : January 15, 2017 Estimated Primary Completion Date : April 1, 2019 Estimated Study Completion Date : June 30, 2019 Resource links provided by the National Library of Medicine related topics: related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: Exercise Intervention Exercise training will take place three times per week for six weeks and involve both aerobic and resistance (...) Sleep Apnea, Cardiovascular and Exercise Study Sleep Apnea, Cardiovascular and Exercise Study - 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. Sleep Apnea, Cardiovascular and Exercise Study The safety

2017 Clinical Trials

15888. A Study Comparing the Safety and Efficacy of Risankizumab to Methotrexate in Subjects With Moderate to Severe Plaque Psoriasis

: risankizumab Drug: methotrexate Phase 3 Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Estimated Enrollment : 100 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: Double (Participant, Investigator) Primary Purpose: Treatment Official Title: A Multicenter, Randomized, Double-Blind, Double-Dummy, Active Controlled Study Comparing the Safety and Efficacy of Risankizumab to Methotrexate in Subjects With Moderate to Severe (...) Plaque Psoriasis Actual Study Start Date : July 30, 2018 Estimated Primary Completion Date : January 21, 2020 Estimated Study Completion Date : September 20, 2021 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Active Comparator: Methotrexate Participants to receive double-blind methotrexate. Drug: methotrexate capsule Experimental: Risankizumab Participants to receive double-blind risankizumab. Drug

2017 Clinical Trials

15889. Dyspareunia and Central Sensitization

Completion Date : August 2021 Resource links provided by the National Library of Medicine related topics: Groups and Cohorts Go to Group/Cohort Intervention/treatment Case Consented to participate in the Data Registry (H16-00264) prior to their physician appointment at the BC Women's Health Centre. New or re-referred to the BC Women's Health Centre for Pelvic Pain and Endometriosis. Endometriosis (previously surgically diagnosed, or current endometrioma, or current nodule) Willing and committed (...) to indicating pain scores and menstrual data on a REDCap survey every day for 6 weeks after the test date. At least 18 years old Other: No Intervention There is no treatment intervention. We are assigning measurement tools such as the Electronic Thimble Algometer for QST and questionnaires to both groups. Control Reproductive aged female with no suspected or diagnosed endometriosis. Have not experienced any sexual pain scores over 4/10 on a 11-point numeric rating scale, as determined on an online

2017 Clinical Trials

15890. SIBO & SIFO After Colectomy

SIBO & SIFO After Colectomy SIBO & SIFO After Colectomy - 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. SIBO & SIFO After Colectomy 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: NCT03216239 Recruitment Status : Completed First Posted : July 13, 2017 Last Update Posted : June 27, 2018 Sponsor: Augusta University Information provided by (Responsible Party): Satish Rao, Augusta University Study Details Study Description Go to Brief Summary: After subtotal colectomy, 40% of patients report abdominal pain, gas

2017 Clinical Trials

15891. Chronic Pain After Childbirth

Chronic Pain After Childbirth Chronic Pain After Childbirth - Caesarean Section Compared to Vaginal Delivery and the Impact of Pre-existing Pain - 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. Chronic Pain (...) Design Go to Layout table for study information Study Type : Observational Actual Enrollment : 355 participants Observational Model: Cohort Time Perspective: Prospective Official Title: Incidence and Predictors of Chronic Pain After Vaginal Childbirth and C-section - a Prospective Cohort Study Actual Study Start Date : January 2013 Actual Primary Completion Date : January 1, 2017 Actual Study Completion Date : June 27, 2017 Resource links provided by the National Library of Medicine related topics

2017 Clinical Trials

15892. A Study of Enfortumab Vedotin for Patients With Locally Advanced or Metastatic Urothelial Bladder Cancer

A Study of Enfortumab Vedotin for Patients With Locally Advanced or Metastatic Urothelial Bladder Cancer A Study of Enfortumab Vedotin for Patients With Locally Advanced or Metastatic Urothelial Bladder Cancer - 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 (...) to a drug that is not part of the treatment effect. Patients who sign up for this trial must also fall into one of these categories: Patients have already received treatment with platinum-containing chemotherapy Patients have never received platinum-containing treatment and are not eligible for treatment with cisplatin. Condition or disease Intervention/treatment Phase Carcinoma, Transitional Cell Urinary Bladder Neoplasms Urologic Neoplasms Renal Pelvis Neoplasms Urothelial Cancer Ureteral Neoplasms

2017 Clinical Trials

15893. Efficacy and Safety of NYX-2925 in Subjects With Neuropathic Pain Associated With Diabetic Peripheral Neuropathy

: Supportive Care Official Title: A Randomized, Double-Blind, Parallel-Group, Placebo-Controlled, Multiple-Dose Study to Assess the Efficacy and Safety of NYX-2925 in Subjects With Neuropathic Pain Associated With Diabetic Peripheral Neuropathy Actual Study Start Date : June 27, 2017 Actual Primary Completion Date : November 2, 2018 Actual Study Completion Date : November 2, 2018 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention (...) anti-inflammatory drugs (except cardiac preventive acetylsalicylic acid), opioids, muscle relaxants, dextromethorphan (except low dose intermittent use for cough), tramadol, topical lidocaine, topical capsaicin, and selective norepinephrine reuptake inhibitors. Subjects are allowed to enter with a maximum of 1 allowed analgesic medication for neuropathic pain that has been taken at stable dose for at least 1 month (30 days) prior to Visit 1. Allowed analgesics may not be N-methyl-D-aspartate

2017 Clinical Trials

15894. Effects of Perioperative Administration of Dexamethasone on Postoperative Complications and Mortality After Non-cardiac Major Surgery

significant risk of anastomotic leakage. At present, no large randomized controlled trial has been performed in patients undergoing major non-cardiac surgery. In acute medicine, several lines of evidence have shown that low to moderate doses of corticosteroids decrease the excessive inflammatory response, without inducing immuno suppression. However, despite the widespread use of corticosteroids to reduce postoperative nausea and vomiting and to improve analgesia, concerns continue to be raised about (...) : a Randomized, Multicentre, Double Blind, Study Actual Study Start Date : December 13, 2017 Estimated Primary Completion Date : December 2019 Estimated Study Completion Date : December 2019 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Experimental: Dexamethasone Standard cares plus postoperative administrations of glucocorticoid Drug: Dexamethasone Dexamethasone : first dose : 0,2mg.kg-1 at the end

2017 Clinical Trials

15895. Which Physical Activity Influences Achilles Tendon Blood Flow the Most?

: a Cohort Study Actual Study Start Date : March 2014 Estimated Primary Completion Date : January 2018 Estimated Study Completion Date : January 2018 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: healthy active participants Other: physical activity Subjects performed five activities: running, static stretch, dynamic stretch, cycling and rope skipping Outcome Measures Go to Primary Outcome Measures : Change (...) Which Physical Activity Influences Achilles Tendon Blood Flow the Most? Which Physical Activity Influences Achilles Tendon Blood Flow the Most? - 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. Which Physical

2017 Clinical Trials

15896. Meditoxin® Treatment in Patients With Cervical Dystonia

Assignment Masking: Double (Participant, Investigator) Primary Purpose: Treatment Official Title: A Prospective, Randomized, Multi-center, Phase III, Double-blind, Placebo-Controlled, Parallel-Group Study to Evaluate the Efficacy and Safety of MEDITOXIN in Treatment of Cervical Dystonia Actual Study Start Date : July 6, 2017 Estimated Primary Completion Date : October 31, 2019 Estimated Study Completion Date : December 31, 2019 Resource links provided by the National Library of Medicine related topics (...) : related topics: resources: Arms and Interventions Go to Arm Intervention/treatment Experimental: MEDITOXIN Drug: Meditoxin Meditoxin (Botulinum toxin type A) Placebo Comparator: Placebo Drug: Placebo Placebo (Normal saline) Outcome Measures Go to Primary Outcome Measures : Change in Toronto Western Spasmodic Torticollis Rating Scale Total Score From Baseline [ Time Frame: week 4 follow-up visit ] Secondary Outcome Measures : Toronto Western Spasmodic Torticollis Rating Scale Severity Subscale

2017 Clinical Trials

15897. A Strategy to Improve Success of Treatment Discontinuation in Buprenorphine Responders

: Interventional (Clinical Trial) Estimated Enrollment : 60 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: None (Open Label) Primary Purpose: Treatment Official Title: A Strategy to Improve Success of Treatment Discontinuation in Buprenorphine Responders Actual Study Start Date : August 1, 2017 Estimated Primary Completion Date : August 1, 2019 Estimated Study Completion Date : December 1, 2019 Resource links provided by the National Library of Medicine related topics (...) A Strategy to Improve Success of Treatment Discontinuation in Buprenorphine Responders A Strategy to Improve Success of Treatment Discontinuation in Buprenorphine Responders - 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

2017 Clinical Trials

15898. Study to Compare the Oestradiol Suppression, Clinical Efficacy and Safety of Two Formulations of Triptorelin (Triptorelin Pamoate PR 3-month and Triptorelin Acetate PR 1-month) in Chinese Subjects With Endometriosis

3 Study Design Go to Layout table for study information Study Type : Interventional (Clinical Trial) Estimated Enrollment : 300 participants Allocation: Randomized Intervention Model: Parallel Assignment Masking: Single (Outcomes Assessor) Primary Purpose: Treatment Official Title: A Phase III, Multicentre, Randomised, Open-label, Parallel, Active-controlled Study to Compare the Oestradiol Suppression, Clinical Efficacy and Safety of Two Formulations of Triptorelin (Triptorelin Pamoate PR 3 (...) -month and Triptorelin Acetate PR 1-month) in Chinese Subjects With Endometriosis Actual Study Start Date : July 28, 2017 Estimated Primary Completion Date : October 31, 2019 Estimated Study Completion Date : February 28, 2020 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Experimental: triptorelin pamoate PR 3-month Drug: Triptorelin Pamoate PR 3-month 15mg/injection, administered as an intramuscular

2017 Clinical Trials

15899. Clinical Benefit of a Mouthrinse for the Treatment of Dentine Hypersensitivity

(Open Label) Primary Purpose: Treatment Official Title: Clinical Benefit of a Mouthrinse for the Treatment of Dentine Hypersensitivity Actual Study Start Date : August 25, 2017 Actual Primary Completion Date : December 7, 2017 Actual Study Completion Date : December 7, 2017 Resource links provided by the National Library of Medicine related topics: Arms and Interventions Go to Arm Intervention/treatment Experimental: Treatment Group Other: Mouthrinse (IQP-OLP-101) Rinse/gargle 10mL of Mouthrinse (...) hypersensitivity to air stimulation → VAS ≥ 40mm at study entry Any sensitive tooth showing exposure of cervical dentine (gum recession) and no acute signs of caries on the exposed root For subjects entering the study at stage PAR-control: good healing of the periodontal surgery site, cause of pain must not be the result of the periodontal surgery Age ≥ 18 years and ≤ 75 years Willing and able to attend the on-study visits Willing and able to understand and to follow the study procedures and instructions Good

2017 Clinical Trials

15900. Vitamin D Supplementation and Tibia Fracture. Does it Improve Healing Rate?

With Operated Tibia Fracture and Low Vitamin D. Does it Improve Healing Rate?. Randomized Controlled Trial Actual Study Start Date : November 21, 2017 Estimated Primary Completion Date : August 18, 2021 Estimated Study Completion Date : August 18, 2023 Resource links provided by the National Library of Medicine related topics: available for: Arms and Interventions Go to Arm Intervention/treatment Experimental: Vitamin D3 supplementation. Deficiency. Vitamin D3 50.000 UI in each packet of powder for solution (...) Vitamin D Supplementation and Tibia Fracture. Does it Improve Healing Rate? Vitamin D Supplementation and Tibia Fracture. Does it Improve Healing Rate? - 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

2017 Clinical Trials

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