Trials / Not Yet Recruiting
Not Yet RecruitingNCT07140510
Dinalbuphine Sebacate in Postoperative Pain Control After TKA
Effectiveness of Dinalbuphine Sebacate in Postoperative Pain Control Following Total Knee Arthroplasty: A Randomized Double Blinded Placebo-controlled Trial
- Status
- Not Yet Recruiting
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- Sponsor
- Thammasat University · Academic / Other
- Sex
- All
- Age
- 50 Years – 90 Years
- Healthy volunteers
- Not accepted
Summary
To evaluate the effectiveness of Dinalbuphine Sebacate for controlling subacute pain after total knee arthroplasty
Detailed description
A single dose of intramuscular Dinalbuphine Sebacate can mitigate pain for up to 1 week after TKA
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Dinalbuphine Sebacate | Dinalbuphine Sebacate 150 mg intramuscular injection after spinal anesthesia and adductor canal block in the same side of TKA |
| DRUG | Normal Saline | Normal saline 2 mL intramuscular injection after spinal anesthesia and adddutor canal block |
Timeline
- Start date
- 2025-10-01
- Primary completion
- 2026-06-01
- Completion
- 2026-09-01
- First posted
- 2025-08-24
- Last updated
- 2025-08-24
Locations
1 site across 1 country: Thailand
Source: ClinicalTrials.gov record NCT07140510. Inclusion in this directory is not an endorsement.