Does Ioband Coverage Waterproof Dressing Provide Better Outcome Than Isolate Waterproof Dressing After Primary Total Knee Arthroplasty? A Prospective Randomized Controlled Trial
Status: Recruiting
Location: See all (2) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY
Conclusion: The trial aims to provide insights into the benefits of Ioband® coverage waterproof dressing in improving post-operative care for TKA patients, focusing on key outcomes related to dressing performance and patient satisfaction.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 55
Healthy Volunteers: t
View:
• Primary unilateral TKA
• Age 55-80 yrs
Locations
Other Locations
Thailand
Department of Orthopaedics, Thammasat University
RECRUITING
Pathum Thani
Thammasat University Hospital
RECRUITING
Pathum Thani
Contact Information
Primary
Krit Boontanapibul, M.D.
krit.boontanapibul@gmail.com
66613957799
Backup
Chanon Thassanaleelaporn, M.D.
C.pond21@gmail.com
Time Frame
Start Date: 2025-04-06
Estimated Completion Date: 2026-04-16
Participants
Target number of participants: 96
Treatments
Active_comparator: Control Group: Isolated waterproof dressing (Opsite®).
Isolated waterproof dressing (Opsite®).
Experimental: Ioban Coverage group
Participants in this group will receive an Ioban iodine-impregnated antimicrobial incise drape placed over the standard water proof dressing at the end of primary total knee arthroplasty.the ioban drape extends 2 cm beyond the edge of the primary dressing and remain in place until dressing remove
Related Therapeutic Areas
Sponsors
Leads: Thammasat University Hospital