Clinical Trials Directory

Trials / Completed

CompletedNCT00146198

Efficacy and Safety of ALGRX 4975 in Treatment of Postoperative Pain After Hernia Repair

A Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Analgesic Efficacy, Safety and Tolerability of ALGRX 4975 in Subjects After Inguinal Hernia Repair

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
40 (planned)
Sponsor
AlgoRx Pharmaceuticals · Industry
Sex
Male
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Hernia repair is one of the most common operations. Whilst there are few complications, pain may last for several weeks and extend the period of convalescence. ALGRX 4975 is an ultra-pure form of capsaicin, which is a pain medicine that has the potential for long-term pain relief following a single administration. This study will determine whether ALGRX 4975 can provide pain relief following hernia repair.

Detailed description

Inguinal hernia correction in adults is one of the most common operations with an annual rate of approximately 2,800 per 1 million people in the United States. Whilst there is little intra and postoperative morbidity, pain may persist for one to several weeks postoperatively and may extend the period of convalescence. ALGRX 4975 is an ultra-pure form of capsaicin, which is a pain medicine that has the potential for long-term pain relief following a single administration. The purpose of this study is to determine whether a single dose of ALGRX 4975, administered by instillation, is able to reduce the postoperative pain following inguinal hernia correction and to evaluate the potential for long term pain relief.

Conditions

Interventions

TypeNameDescription
DRUGALGRX 4975

Timeline

Start date
2005-09-01
Completion
2006-02-01
First posted
2005-09-07
Last updated
2006-12-20

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT00146198. Inclusion in this directory is not an endorsement.