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NCT06312527
Mepiform in Simultaneous Bilateral TKA
NA trial testing Silicone dressing in Scar Prevention in 30 participants. Participants enrolled and being followed up; not accepting new ones.
31 May 2024
Quick facts
| Lead sponsor | Thammasat University Hospital |
|---|---|
| Phase | NA |
| Status | Active, enrolled |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | double |
| Primary purpose | treatment |
| Enrollment | 30 |
| Start date | 7 March 2024 |
| Primary completion | 31 May 2024 |
| Estimated completion | 31 May 2025 |
| Sites | 1 location across Thailand |
Drugs / interventions tested
- Silicone dressing
Conditions studied
- Scar Prevention — all drugs for Scar Prevention →
Sponsor
Thammasat University Hospital
Who can join
Adults 50 to 80, any sex, with Scar Prevention. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The goal of this RCT is comparing efficacy of silicone dressing in scar preventing after simultaneous bilateral total knee arthroplasty. The main question\[s\] it aims to answer are: * Does silicone dressing can prevent scar formation after total knee arthroplasty? * Does silicone dressing have similar functional outcomes and complications after total knee arthroplasty? Participants will apply silicone dressing after wound healed and apply for 10 weeks. Researchers will compare to the other side that is no intervention.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT06312527
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
Related trials
Other Thammasat University Hospital trials
Trials by the same sponsor.
- NCT06910930 — Impact of Muscle Training Device on Non-Severe OSA · NA · recruiting
- NCT06943053 — Evaluation of Ioband Coverage Waterproof Dressing Versus Isolated Waterproof Dressing After Primary Total Knee Arthropla · NA · recruiting
- NCT06800846 — Comparative Analgesic Effect After Total Knee Arthroplasty Between Intraosseous and Peri-articular Injection · Phase 4 · enrolling by invitation
- NCT06328062 — Comparing Efficiency of Mirogabalin and Pregabalin in Primary TKA · NA · recruiting
- NCT06323577 — Comparing Efficacy Between Restricted Kinematic Alignment vs Mechanical Alignment in Bilateral TKA · NA · recruiting
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06312527 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Thammasat University Hospital
- Last refreshed: 9 April 2025
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06312527.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing