Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
270 participants
INTERVENTIONAL
2021-04-19
2023-11-11
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Non absorbable suture
Wound closure with non absorbale suture. Dimension and brand at the discretion of the surgeon.
Skin closure
Skin closure
Absorbable suture
Wound closure with absorbale suture. Dimension and brand at the discretion of the surgeon.
Skin closure
Skin closure
Interventions
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Skin closure
Skin closure
Eligibility Criteria
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Exclusion Criteria
* Patients with known healing problems in the past, for example patients with burns or during cortisone treatment.
* Patients undergoing surgery where skin grafting occurs.
* Patients with acute injuries that include a traumatic wound-ie what is usually referred to as "open injuries" -where the risk of infection is higher from the beginning.
18 Years
99 Years
ALL
No
Sponsors
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Department of Hand surgery Södersjukhuset
OTHER
Responsible Party
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Mirjam Hägg
Resident Physician
Locations
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Södersjukhuset Hospital
Stockholm, , Sweden
Countries
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Other Identifiers
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2020-06004
Identifier Type: -
Identifier Source: org_study_id