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The effect of Suturing Techniques on aberrant wound recovery after Total Hip Arthroplasty

Conditions
hip prothesis.
skin closure method. Total Hip Arthroplasty
Suturing techniques
10005944
Registration Number
NL-OMON56640
Lead Sponsor
Reinier Haga Orthopedisch Centrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Not specified
Target Recruitment
236
Inclusion Criteria

• >= Eighteen years old
• Scheduled to undergo a primary THA via the anterior approach by one of the
participating surgeons, for any indication
• No prior operations of the hip which is to be operated on for this study
• Able to provide written informed consent
• Patient is able to speak and write in Dutch

Exclusion Criteria

• Use of cytostatic substances in the period ranging from fourteen days prior,
to ninety days after the surgery.
• Difficulty with or inability to communicate with the investigators (e.g.
difficulty with the Dutch language, cognitive /memory disorder).

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The main study parameter is aberrant wound recovery after three days and<br /><br>fourteen days postoperatively in patients after a THA. </p><br>
Secondary Outcome Measures
NameTimeMethod
<p>Secondary outcomes are the occurrence of superficial- and deep wound infections<br /><br>for the four suturing techniques during hospitalisation, fourteen days<br /><br>postoperatively, and ninety days postoperatively, as well as the costs of each<br /><br>of the suturing techniques, and whether, or not, patients have to visit the<br /><br>outpatient clinic for a control appointment in standard care.</p><br>
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