Evaluation of Ioband Coverage Waterproof Dressing Versus Isolated Waterproof Dressing After Primary Total Knee Arthroplasty
Sponsored by Thammasat University Hospital
About this trial
Last updated a year ago
Study ID
TUH wound coverage after TKA
Status
Recruiting
Type
Interventional
Phase
N/A
Placebo
No
Accepting
55+ Years
All Sexes
Trial Timing
Ended 11 days ago
What is this trial about?
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.
What are the participation requirements?
Inclusion Criteria
* Primary unilateral TKA
* Age 55-80 yrs
Exclusion Criteria
* Chronic Skin disease such as Psoriasis
* Chronic steroid use
* Allergy to skin adhesive, Cover wound
* Robotic TKA
* Iodine allergy
* Not follow protocol
