HIP-STITCH (Wound Recovery After THA)
Recruiting
N/A
Interventional Study
Wound Healing Disturbance of
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 236 (estimated)
- Sponsor
- Reinier Haga Orthopedisch Centrum · Other
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About This Trial
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 oper…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 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.
Exclus…
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