CompletedNot Applicable

Dermal Wound Closure Using Silkam®

Spain161 participantsStarted 2022-07-21

Plain-language summary

Assessment of performance of Silkam® suture material for skin closure. A prospective, single center, single arm, observational study in daily practice.

Who can participate

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Adult and paediatric patients undergoing skin closure using Silkam® as suture material. * Written informed consent regarding the data collection for the PMCF study. Exclusion Criteria: * Pregnancy * Visible dirty wounds * Patients taking medication that might affect wound healing * Patients with hypersensitivity or allergy to the suture material

What they're measuring

Surgical Site Infection Rate

Timeframe: at suture removal approx. 10 ± 5 days postoperative

Trial details

NCT IDNCT05225714

SponsorAesculap AG

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2025-06-25

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