Trials / Completed
CompletedNCT05139875
Comparing Intra-articular Betamethasone (Diprospan) and Triamcinolone Acetonide Injection in Knee Osteoarthritis
A Comparative Study of Betamethasone (Diprospan) and Triamcinolone Acetonide as Single Intra-Articular Injection in Knee Osteoarthritis, A Double-Blinded, Randomized Controlled Trial
- Status
- Completed
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 105 (actual)
- Sponsor
- Thammasat University · Academic / Other
- Sex
- All
- Age
- —
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to compare the efficacy of Intra-articular corticosteroid injection between Betamethasone (Diprospan) and Triamcinolone acetonide for treatment of knee osteoarthritis
Detailed description
After being informed about the study and potential risks, all patients giving written informed consent will be chosen for eligibility for the study entry. At day 0 (before intra-articular injection), patients who meet the eligibility criteria will be randomized in a double-blind manner (participant and investigator) in a 1:1 ratio to Betamethasone (Diprospan 1 ml) or Triamcinolone acetonide (40 mg) single intra-articular injection
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Betamethasone Dipropionate / Betamethasone Sodium Phosphate | Single intra-articular Betamethasone Dipropionate / Betamethasone Sodium Phosphate (Diprospan) injections to affected knee |
| DRUG | Triamcinolone Acetonide 40mg/mL | Single intra-articular Triamcinolone Acetonide injections to affected knee |
Timeline
- Start date
- 2022-01-01
- Primary completion
- 2024-04-30
- Completion
- 2024-04-30
- First posted
- 2021-12-01
- Last updated
- 2024-08-30
Locations
1 site across 1 country: Thailand
Source: ClinicalTrials.gov record NCT05139875. Inclusion in this directory is not an endorsement.