Trials / Active Not Recruiting
Active Not RecruitingNCT06742554
Comparative Efficacy of Buprenorphine Transdermal Patch Versus Tramadol in Postoperative Analgesia for Shoulder Arthroscopy
Comparative Efficacy of Buprenorphine Transdermal Patch Versus Tramadol in Postoperative Analgesia for Shoulder Arthroscopy: a Randomized Controlled Trial.
- Status
- Active Not Recruiting
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 70 (estimated)
- Sponsor
- medina medical center · Academic / Other
- Sex
- All
- Age
- 18 Years – 65 Years
- Healthy volunteers
- Not accepted
Summary
This study compares the efficacy, safety, and patient satisfaction of the Buprenorphine 10 mg transdermal patch versus Tramadol for postoperative analgesia in shoulder arthroscopic surgery. The study hypothesizes that Buprenorphine provides superior pain relief with fewer side effects compared to Tramadol.
Conditions
- Postoperative Pain
- Shoulder Pain
- Opioid Analgesia
- Tramadol
- Buprenorphine
- Arthroscopy
- Interscalene Brachial Plexus Block
- Analgesic
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Buprenorphine transdermal patch | Buprenorphine Transdermal Patch (10 mg): Applied once before surgery for continuous pain control. Interscalene Brachial Plexus Block: Administered intraoperatively using 25 mL of 0.5% bupivacaine. |
| DRUG | Tramadol | Tramadol: Administered orally or intravenously at a standard dose of 100 mg every 8 hours, based on patient-reported pain levels. Interscalene Brachial Plexus Block: Administered intraoperatively using 25 mL of 0.5% bupivacaine. |
Timeline
- Start date
- 2024-12-01
- Primary completion
- 2025-04-01
- Completion
- 2025-04-30
- First posted
- 2024-12-19
- Last updated
- 2024-12-20
Locations
1 site across 1 country: Saudi Arabia
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT06742554. Inclusion in this directory is not an endorsement.