Clinical Trials Directory

Trials / Completed

CompletedNCT06766474

The Rule of Bupivacaine Hydrochloride in Skin Graft Donor Site

Bupivacaine Hydrochloride-Soaked Dressing Versus Subcutaneous Infiltration for Postoperative Analgesia in Skin Graft Donor Site: a Randomized Controlled Clinical Trial

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
90 (actual)
Sponsor
Minia University · Academic / Other
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

Split Thickness Skin Graft is frequently utilized for reconstructing skin loss of various causes. Unfortunately, the donor site of the STSG has an unavoidable, annoying post-operative pain

Detailed description

The primary objective of this study was to compare the efficacy of bupivacaine hydrochloride-soaked dressing versus bupivacaine HCL subcutaneous infiltration for postoperative donor site pain control for patients undergoing STSG procedures. The patients were divided in 3 equal groups, investigated soaked dressing vs subcutaneous infiltration vs conventional dressing .

Conditions

Interventions

TypeNameDescription
DRUGBupivacainto our knowledge, this study is the 1st to compare the efficacy of bupivacaine hydrochloride-soaked dressing versus subcutaneous infiltration for postoperative donor site pain control for patients undergoing STSG procedures.

Timeline

Start date
2023-03-01
Primary completion
2024-10-15
Completion
2024-10-30
First posted
2025-01-09
Last updated
2025-01-13

Locations

1 site across 1 country: Egypt

Regulatory

Source: ClinicalTrials.gov record NCT06766474. Inclusion in this directory is not an endorsement.