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Bunion clinical trials

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NCT ID: NCT01791634 Completed - Hallux Valgus Clinical Trials

Prospective, Multi-Center Clinical Evaluation of the Open Wedge Osteotomy and Low Profile Plate & Screw (LPS) System Compared to the Proximal Chevron Osteotomy for the Treatment of Hallux Valgus With an Increased Intermetatarsal Angle

Hallux valgus
Start date: April 2007
Phase: N/A
Study type: Interventional

Is there a difference in clinical outcome measures as assessed by the AOFAS, SF-36 and Visual Analogue Scale of adult patients with moderate to severe hallux valgus with increased intermetatarsal angles treated with a proximal open wedge osteotomy with LPS system versus the proximal chevron osteotomy?

NCT ID: NCT01743625 Completed - Pain, Postoperative Clinical Trials

Safety and Efficacy Study of COV155 for Post-operative Bunionectomy Pain

Start date: November 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to show the effectiveness of COV155 compared to placebo in subjects with acute moderate to severe pain following bunionectomy surgery.

NCT ID: NCT01484652 Completed - Pain, Postoperative Clinical Trials

Safety and Efficacy of COV795 in Moderate to Severe Post-Operative Bunionectomy Pain With an Open-label Extension

Start date: November 2011
Phase: Phase 3
Study type: Interventional

The primary objective of this study is to show the effectiveness of repeated doses of COV795 versus placebo, using the summed pain intensity difference over the first 48 hours in subjects with acute moderate to severe pain following bunionectomy.

NCT ID: NCT01435577 Completed - Pain Clinical Trials

Intravenous Tapentadol in Post-Bunionectomy Pain

Start date: September 2011
Phase: Phase 2
Study type: Interventional

The purpose of this trial is to established the safety and efficacy of multiple dose treatment with tapentadol IV in an adult population with moderate to severe pain following bunionectomy.

NCT ID: NCT00890682 Completed - Hallux Valgus Clinical Trials

Study of Postoperative Analgesia in Bunionectomy

Start date: April 2009
Phase: Phase 3
Study type: Interventional

After undergoing bunion surgery, patients are given a pain medicine injection that may last for up to several days or a placebo. Their pain and pain medicine use is then monitored.

NCT ID: NCT00613938 Completed - Pain Clinical Trials

A Study to Evaluate the Effectiveness and Safety of Tapentadol (CG5503) in the Treatment of Acute Pain From Bunionectomy.

Start date: February 2008
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the effectiveness (level of pain control) and safety of the administration of 2 different dose levels of tapentadol (CG5503) compared with oxycodone and with placebo in subjects who have had a bunionectomy.

NCT ID: NCT00364247 Completed - Hallux Valgus Clinical Trials

A Study to Evaluate the Effectiveness and Safety of Tapentadol(CG5503) in the Treatment of Acute Pain From Bunionectomy Compared With Placebo Followed by a Voluntary Open Label Extension for Safety.

Start date: n/a
Phase: Phase 3
Study type: Interventional

The purpose of this study is to evaluate the effectiveness (level of pain control) and safety of the administration of 3 different dose levels of CG5503 compared with oxycodone and with placebo in patients who have had a bunionectomy, and to assess the safety of the drug for 9 days after patients are discharged from the hospital.