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Novosyn® Quick in Patients Undergoing Episiotomy Closure

Novosyn® Quick in Patients Undergoing Episiotomy Closure

Recruiting
18 years and older
Female
Phase N/A
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  • Simplified (AI rewritten)

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Overview

Retrospective, monocentric clinical study on the clinical performance of Novosyn® Quick in patients undergoing episiotomy closure.

Description

The study design is a retrospective, consecutive series of women with a spontaneous vaginal delivery who required an indicated episiotomy with Novosyn® Quick between the period January 2020 - December 2020 at Hospital General de Catalunya.

All women treated with Novosyn® Quick between January 2020 - December 2020 at the Hospital General de Catalunya will be analyzed. The investigator team will access medical records for the cohort of patients identified.

Eligibility

Inclusion Criteria:

  • Women who underwent an indicated episiotomy between January 2020 - December 2020 at the Hospital General de Catalunya (Sant Cugat del Vallès, Spain) and received Novosyn® Quick

Exclusion Criteria:

  • No exclusion criteria have been set

Study details
    Episiotomy Wound

NCT05233527

Aesculap AG

6 September 2025

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