Evaluation of Ioband Coverage Waterproof Dressing Versus Isolated Waterproof Dressing After Primary Total Knee Arthroplasty
Recruiting now · Not applicable
Conditions studied: Postoperative Wound Care After TKA
In brief
Title: Evaluation of Ioband® Coverage Waterproof Dressing in Post-Operative Total Knee Arthroplasty (TKA) Goal: To evaluate the effectiveness of Ioband® coverage waterproof dressing compared to standard waterproof dressing in reducing dressing change frequency and peel-off degree post-op TKA. Main Research Questions: 1. Does Ioband® coverage waterproof dressing significantly decrease the degree of peel-off compared to standard waterproof dressing? 2. Does Ioband® coverage reduce the number of wound dressing changes required post-operatively? 3. Does Ioband® coverage improve overall patient satisfaction compared to standard waterproof dressing? Participants: Participants will include patients who have undergone total knee arthroplasty (TKA). Main Tasks and Interventions: 1. Randomization: Participants will be randomly assigned to receive either the Ioband® coverage waterproof dressing or the standard waterproof dressing. 2. Application of Dressings: Participants will have the assigned dressing applied to their surgical site post-operatively. 3. Assessment of Peel-Off Degree: Participants will undergo assessments to evaluate the degree of peel-off of the dressing over a specified time. 4. Wound Dressing Changes: Participants will have their dressing changed as per routine care protocols, with documentation of the number of changes. 5. Patient Satisfaction Survey: Participants will complete a satisfaction survey to assess their experiences with the dressing and overall comfort. 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.
Key facts
- Study ID
- NCT06943053
- Run by
- Thammasat University Hospital
- People needed
- 96
- Starts
- 2025-04-06
- Expected to finish
- 2026-04-16
- Last updated by the study team
- 2025-04-24
Who can join
Age: 55 and older. Sex: any. Healthy volunteers: accepted.
You may qualify if…
- Primary unilateral TKA
- Age 55-80 yrs
You may not qualify if…
- Chronic Skin disease such as Psoriasis
- Chronic steroid use
- Allergy to skin adhesive, Cover wound
- Robotic TKA
- Iodine allergy
- Not follow protocol
Where it is running
- Thammasat University Hospital — Pathum Thani, Khlong luang, Thailand (enrolling)
- Department of Orthopaedics, Thammasat University — Pathum Thani, Thailand (enrolling)
Full record on ClinicalTrials.gov
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