Clinical Trials Directory

Trials / Completed

CompletedNCT04754451

The Effect of Lidocaine Patch for Postoperative Pain

The Efficacy and Safety of 5% Lidocaine Patch for Postoperative Pain in Unilateral Inguinal Herniorrhaphy

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
32 (actual)
Sponsor
BON WOOK KOO · Academic / Other
Sex
All
Age
19 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The lidocaine patch is currently only permitted for post herpetic neuralgia but the investigators want to study its effectiveness in post operative pain after inguinal herniorrhaphy

Detailed description

After open unilateral inguinal herniorrhaphy, patients are randomly divided into group L and group P groups. Group L attaches two lidocaine patches for 12 hours, above and below the incision site. Group P attaches two placebo patches for 12 hours, above and below the incision site. Pain scores are recorded for 30 minutes, 2 hours, 24 hours, and 1 week after surgery.

Conditions

Interventions

TypeNameDescription
DRUGGroup LAttach two lidocaine patches for 12 hours, one above and below the incision site.

Timeline

Start date
2021-03-15
Primary completion
2022-11-23
Completion
2022-11-30
First posted
2021-02-15
Last updated
2023-12-26

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT04754451. Inclusion in this directory is not an endorsement.

The Effect of Lidocaine Patch for Postoperative Pain (NCT04754451) · Clinical Trials Directory