Clinical Trials Logo

Filter by:
NCT ID: NCT03106545 Completed - Clinical trials for Hallux Valgus (Bunions)

Liposome Bupivacaine for ANKLE Blocks

Start date: January 2, 2017
Phase: Phase 2
Study type: Interventional

Postoperative analgesia for hallux valgus surgery (bunionectomy) is inconsistent and may even result in rebound pain when the (ankle) blocks wear off. It is hypothesized that the mixture of bupivacaine and liposome bupivacaine increases the extent and duration of postoperative analgesia and decreases opioid consumption as compared to bupivacaine alone or to general anesthesia.

NCT ID: NCT03106519 Completed - Clinical trials for Dupuytren's Contracture of the Hand (Viking's Disease)

Liposome Bupivacaine for WRIST Blocks

Start date: January 2, 2017
Phase: Phase 2
Study type: Interventional

Treatment of Dupuytren's contracture requires multiple injections into the palm of the hand to weaken the cords, followed by rupture of the strands 2 days later. Anesthesia is required for both phases of treatment. It is hypothesized that extended-release liposome bupivacaine prolongs nerve blockade of the wrist allowing patients to undergo this 2-part regimen with less pain.

NCT ID: NCT03106194 Completed - Clinical trials for Drug Abuse, Intravenous

Case Management in HCV Infected PWID

CM-HCV
Start date: July 2016
Phase: N/A
Study type: Interventional

To study the impact of case management on the outcome of the care of chronic hepatitis C in people who inject drugs (PWID). By creating the function of case manager, the investigators will target all the barriers to care of the HCV care continuum. Partial objectives are to measure the impact of case management on the uptake for screening, the uptake and outcome of treatment, and the rate of reinfection.

NCT ID: NCT03106142 Completed - Knee Osteoarthritis Clinical Trials

Knee Osteoarthritis Care: A Quality Improvement Intervention in General Practice

Start date: September 2014
Phase: N/A
Study type: Interventional

The aim of this study is to improve the referral rates to physiotherapy of patients with knee osteoarthritis. The intervention consists of one academic detailing visit directed to general practitioners (GPs)

NCT ID: NCT03105453 Completed - Infertility Clinical Trials

The Microbiome in Subfertility and Assisted Reproductive Technologies (ART)

Start date: September 2016
Phase:
Study type: Observational

To assess the impact of the female genital microbiome on ART outcome.

NCT ID: NCT03105128 Completed - Crohn's Disease Clinical Trials

A Study of the Efficacy and Safety of Risankizumab in Participants With Moderately to Severely Active Crohn's Disease

Start date: May 10, 2017
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of risankizumab versus placebo during induction therapy in participants with moderately to severely active Crohn's disease (CD).

NCT ID: NCT03104699 Completed - Cervical Cancer Clinical Trials

Study of AGEN2034 in Advanced Tumors and Cervical Cancer

Start date: April 11, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

This is a 2-part trial: a Phase 1, open-label, dose-escalation study in subjects with metastatic or locally advanced solid tumors, with a consecutive Phase 2 expansion to evaluate efficacy in subjects with recurrent, unresectable, or metastatic (advanced) cervical cancer that has progressed after a platinum-based treatment regimen.

NCT ID: NCT03104413 Completed - Crohn's Disease Clinical Trials

A Study to Assess the Efficacy and Safety of Risankizumab in Participants With Moderately to Severely Active Crohn's Disease Who Failed Prior Biologic Treatment

Start date: December 18, 2017
Phase: Phase 3
Study type: Interventional

The objective of Study M15-991 is to evaluate the efficacy and safety of risankizumab versus placebo during induction therapy in participants with moderately to severely active CD.

NCT ID: NCT03103087 Completed - Uterine Fibroid Clinical Trials

LIBERTY 2: Efficacy & Safety Study of Relugolix in Women With Heavy Menstrual Bleeding Associated With Uterine Fibroids

Start date: June 14, 2017
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine the benefit of relugolix 40 milligrams (mg) once a day co-administered with estradiol (E2) 1 mg and norethindrone acetate (NETA) 0.5 mg compared with placebo for 24 weeks on heavy menstrual bleeding associated with uterine fibroids.

NCT ID: NCT03102671 Completed - Clinical trials for Coronary Artery Disease

Effectiveness of the HeartHab Application on Exercise Capacity in Patients With Coronary Artery Disease

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

The recurrence of major cardiac events after infarction is very high, in some populations up to 20% in the first year. Optimal secondary prevention as organized in cardiac rehabilitation centers is effective in reducing both morbidity and mortality. However, many studies have shown that the participation and adherence rate in CR-programs is low in most European countries. Therefore, novel ways of delivering secondary prevention using information technology and self-monitoring are being explored. Hence, this study will investigate the effectiveness of a mobile, patient tailored, app based multidisciplinary telerehabilitation program (HeartHab app) in improving exercise capacity, lifestyle and risk factors in patients with coronary artery disease in a post-rehabilitation setting.