Novosyn® Quick in Patients Undergoing Episiotomy Closure (RETRO-EPINOQ)

Aesculap

Status: Enrolling

Conditions: Episiotomy Wound

Treatments: Procedure: Episiotomy Closure

Study type: Observational

Funder types: Industry

Identifiers

NCT05233527

AAG-O-H-2111

Details and patient eligibility

About

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

Full 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.

Enrollment: 300 estimated patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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