Actively Recruiting
HIP-STITCH (Wound Recovery After THA)
Led by Reinier Haga Orthopedisch Centrum · Updated on 2024-10-24
236
Participants Needed
1
Research Sites
191 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This prospective randomised trial will investigate the effect of four different suturing techniques (Monocryl, Vicryl Rapide with Indermil skin glue, Dermabond Prineo, and Stryker Zip) on the amount of aberrant wound recovery within 14 days after total hip arthroplasty at the RHOC in Zoetermeer, The Netherlands. This will be done by assessing photographs of the plaster and photographs of the operation wound with a self-developed classification model. The photographs of the plaster will be taken by the test subject at home at 3 days and 11 days postoperatively. The photographs of the operation wound will be taken by a member of the research team, and the doctor's assistant, respectively, during a visit to the outpatient clinic at 7 days and 14 days postoperatively. Hypothesis: Monocryl sutures give the highest amount of aberrant wound recovery within fourteen days after primary THA.
CONDITIONS
Official Title
HIP-STITCH (Wound Recovery After THA)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Eighteen years or older.
- Scheduled to undergo Total Hip Arthroplasty via the anterior approach for any indication at the RHOC.
- No prior operations to the hip which is to be operated on.
- A good command of the Dutch language
- Able to give written informed consent.
You will not qualify if you...
- Usage of cytostatics in the period ranging from fourteen days prior, to ninety days after the operation.
- Unable to, or difficulty with communicating in the Dutch language (e.g. due to mental disability, inability to understand/speak/write Dutch, et cetera).
AI-Screening
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Trial Site Locations
Total: 1 location
1
Reinier Haga Orthopedisch Centrum
Zoetermeer, South Holland, Netherlands, 2725NA
Actively Recruiting
Research Team
B
Brechtje Hesseling, Msc
CONTACT
N
Nina MC Mathijssen, Dr.
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
4
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