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Mepiform in Simultaneous Bilateral TKA

NCT06312527 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2025-04-09

No results posted yet for this study

Summary

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.

Conditions

  • Scar Prevention

Interventions

DEVICE

Silicone dressing

Participant will apply silicone dressing at 2 weeks after TKA on one side of knee. Silicone dressing will change every week until 12 week postoperative.

Sponsors & Collaborators

  • Thammasat University Hospital

    lead OTHER

Principal Investigators

  • Yot Tanariyakul, M.D. · Department of orthopedics

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
50 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-03-07
Primary Completion
2024-05-31
Completion
2025-05-31

Countries

  • Thailand

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06312527 on ClinicalTrials.gov