Clinical Trials Directory

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

TypeNameDescription
DRUGBetamethasone Dipropionate / Betamethasone Sodium PhosphateSingle intra-articular Betamethasone Dipropionate / Betamethasone Sodium Phosphate (Diprospan) injections to affected knee
DRUGTriamcinolone Acetonide 40mg/mLSingle 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.