CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 29 enrolled
Drug / intervention
Su2ura Approximation Device +1 moredevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04393532
NCT04393532N/ACompleted

Laparoscopic Primary Umbilical Hernia Repair With Routine Defect Closure Using Su2ura Approximation Device

Anchora Medical·interventional·Posted May 19, 2020·Updated Jan 22, 2025

In Brief

A clinical study evaluating Su2ura Approximation Device and Laparoscopic hernia repair surgery for Primary Umbilical Hernia. Completed, enrolled 29 participants across 3 sites in 2 countries.

Detailed Summary

Intended Use The Su2ura™ Approximation Device is indicated for tissue approximation in endoscopic and open surgery for the placement of interrupted or running stitches in soft tissue such as hernia repair Objectives To assess the safety and efficacy of the Su2ura approximation device for the laparoscopic repair of primary umbilical hernia Number of Subjects 45 patients Number of Centers Two study centers in Israel and one in Slovenia. Study Duration 6 months Study Procedures Surgery will be performed under general anesthesia. Standard antibiotic prophylaxis will be administered at induction of anesthesia. A single surgeon, the PI, will perform the procedure. A surgical assistant will be selected by the PI from the surgical staff of the department. The procedure will involve placement of laparoscopic ports, reduction of the hernia sac, closure of the defect with the Su2ura approximation device and fixation of mesh with tacks over the closed defect. Study follow up visits: at post operation discharge, 14 days, 3 months, 6 months. Study follow up procedures: Also include SAE's and SADE's during follow up 1. Quality of life questionnaire: patient-reported satisfaction and function will be assessed through the validated, hernia-specific European Hernia Society Quality of Life questionnaire (EuraHS-QoL) 2. Clinical testing to determine hernia recurrence and clinical bulging Statistical analysis The sample size calculation based on the Exact Binomial distribution. The investigators will compute the 95% confidence intervals for a binomial probability, relying on the Clopper-Pearson (exact) method.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesIsrael, Slovenia
Collaborators--

Timeline

N/ACompletedFinished
2020202120222023202420252026
First PostedMay 19, 2020
Enrollment StartFeb 23, 2020
Primary CompletionJan 28, 2024
Study CompletionApr 18, 2024
TodayJul 2, 2026
Enrollment to primary: 3.9 yearsPosted 6.1 years ago

Interventions

Su2ura Approximation Devicedevice

the use of the study device during a laparoscopic surgery

Laparoscopic hernia repair surgeryprocedure

repairing primary umbilical hernia in a laparoscopic procedure using the study device.