Status:
RECRUITING
Performance of SYMMCORA® vs. V-Loc® Suture Material in Patients Undergoing Laparoscopic Total Hysterectomy
Lead Sponsor:
Aesculap AG
Collaborating Sponsors:
B.Braun Surgical SA
Conditions:
Abnormal Uterine Bleeding
Endometriosis
Eligibility:
FEMALE
18+ years
Brief Summary
The aim of this study is to show the superiority of the new unidirectional barbed suture (SYMMCORA® mid-term, unidirectional) to conventional suture material in terms of time to perform the vaginal cu...
Eligibility Criteria
Inclusion
- Females undergoing an elective, laparoscopic total hysterectomy
- Age ≥ 18 years
- Written informed consent
Exclusion
- Emergency surgery
- Open surgery
- Patients undergone immunosuppressive drug treatment within the prior 6 months
- Patients with hypersensitivity or allergy to the suture material.
- Participation in another clinical study
- Non-compliance of patient
Key Trial Info
Start Date :
March 19 2024
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
January 1 2027
Estimated Enrollment :
132 Patients enrolled
Trial Details
Trial ID
NCT06024109
Start Date
March 19 2024
End Date
January 1 2027
Last Update
May 13 2025
Active Locations (2)
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1
Klinikum Sachsenhausen der DGD
Frankfurt am Main, Hesse, Germany, 60594
2
Hospital Sant Joan de Déu de Manresa
Manresa, Barcelona, Spain, 08243