Effectiveness of Per-Operative Bupivicaine in Reducing Postoperative Pain at Port Site and Improving Mobility in Knee Arthoscopic Procedures
Recruiting now · Phase 4 · Has a placebo group
Conditions studied: Arthroscopic Surgery
In brief
The investigator's aim is to evaluate the effectiveness of per-operative bupivacaine infiltration at arthroscopic port sites in reducing post-operative pain compared to placebo in patients undergoing knee arthroscopic procedures.
Key facts
- Study ID
- NCT07090928
- Run by
- Khyber Teaching Hospital
- People needed
- 60
- Starts
- 2026-03-10
- Expected to finish
- 2026-06-01
- Last updated by the study team
- 2026-06-25
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Khyber teaching Hospital Peshawer — Peshawar, KPK, Pakistan (enrolling)
Full record on ClinicalTrials.gov
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