Clinical Performance of HISTOACRYL® LAPFIX - CANNULA for Laparoscopic Inguinal Hernia Repair
NCT ID: NCT06298500
Last Updated: 2025-08-20
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
443 participants
OBSERVATIONAL
2024-03-15
2025-05-07
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Histoacryl Lapfix
Histoacryl Lapfix - Cannula for laparoscopic mesh fixation in patients undergoing hernia repair surgery
hernia repair surgery
In recent years, atraumatic mesh fixation with tissue adhesive has increasingly become the method of choice. It is the recommended mesh fixation method by the International Hernia Society Guidelines. In this study patients with inguinal hernia are treated by placing a prosthetic mesh in one of the layers of the abdominal wall to cover the weakness, the mesh is fixed by Histoacryl LapFix,
Interventions
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hernia repair surgery
In recent years, atraumatic mesh fixation with tissue adhesive has increasingly become the method of choice. It is the recommended mesh fixation method by the International Hernia Society Guidelines. In this study patients with inguinal hernia are treated by placing a prosthetic mesh in one of the layers of the abdominal wall to cover the weakness, the mesh is fixed by Histoacryl LapFix,
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* treated between June 2018 and March 2021 at the Hospital San Juan de Dios for laparoscopic mesh fixation with Histoacryl Lapfix - Cannula after inguinal hernia repair surgery.
18 Years
ALL
No
Sponsors
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B.Braun Surgical SA
INDUSTRY
Aesculap AG
INDUSTRY
Responsible Party
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Locations
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Hospital San Juan de Dios
Santa Cruz de Tenerife, Tenerife, Spain
Countries
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Other Identifiers
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AAG-O-H-2115
Identifier Type: -
Identifier Source: org_study_id
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