Trials / Completed
CompletedNCT02065804
Trigger-point Blockade in Persistent Pain After Laparoscopical Groin Hernia Repair
Trigger-point Blockade in Persistent Pain After Laparoscopically Assisted Groin Hernia Repair
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 14 (actual)
- Sponsor
- University of Copenhagen · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Groin hernia repair is a common procedure performed in approximately 2,000 patients per one million inhabitants. Severe chronic pain following groin hernia repair is seen in 2-5% of the patients indicating that a large number of patients each year suffer from debilitating reduction in health-related quality of life. This study examines the effect of ultra-sound guided blocks with local anesthesia in the groin in regard to pain relief and sleep quality. The hypothesis of the study is that a block will confer significant pain relief to patients with severe chronic pain following laparoscopical groin hernia repair.
Detailed description
This placebo-controlled, randomized, double-blind, cross-over study in subjects with severe pain after laparoscopically assisted groin hernia repair, examines the effect of an ultra-sound guided local anesthetic block of a trigger-point, situated near the spermatic cord at the superficial inguinal ring.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Bupivacaine | injection, once, 5 min |
Timeline
- Start date
- 2013-10-01
- Primary completion
- 2014-07-01
- Completion
- 2014-07-01
- First posted
- 2014-02-19
- Last updated
- 2017-10-18
Locations
1 site across 1 country: Denmark
Source: ClinicalTrials.gov record NCT02065804. Inclusion in this directory is not an endorsement.