Viewing Study NCT06298500



Ignite Creation Date: 2024-05-06 @ 8:12 PM
Last Modification Date: 2024-10-26 @ 3:23 PM
Study NCT ID: NCT06298500
Status: RECRUITING
Last Update Posted: 2024-03-08
First Post: 2024-03-01

Brief Title: Clinical Performance of HISTOACRYL LAPFIX - CANNULA for Laparoscopic Inguinal Hernia Repair
Sponsor: Aesculap AG
Organization: Aesculap AG

Study Overview

Official Title: Retrospective Single Center Clinical Study on the Clinical Performance of Histoacryl Lapfix - Cannula for Laparoscopic Inguinal Hernia Repair
Status: RECRUITING
Status Verified Date: 2024-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: HISTOLAP
Brief Summary: The goal of this retrospective study is to identify the incidence of hernia recurrence following the application of Histoacryl Lapfix - Cannula for laparoscopic mesh fixation in patients undergoing hernia repair surgery All adult patients who underwent laparoscopic inguinal hernia repair with Histoacryl Lapfix - Cannula in the period June 2018 - March 2021 at Hospital San Juan de Dios will be analysed The investigator team will access electronical medical records for the cohort of patients identified
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None