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Laparscopic Inguinal Hernia Repair - Does the Choice of Self-fixated Mesh Matter?

NCT05091853 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 174

Last updated 2024-10-02

No results posted yet for this study

Summary

Self-fixed mesh and postoperative pain after laparoscopic inguinal hernia surgery, a randomized clinical trial

Conditions

  • Inguinal Hernia
  • Surgery

Interventions

DEVICE

Adhesix mesh

2 meshes are used; the self-gripping Progrip mesh and the self-adhesive Adhesix mesh

Sponsors & Collaborators

  • Helsinki University Central Hospital

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-05-09
Primary Completion
2023-07-31
Completion
2024-06-30

Countries

  • Finland

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05091853 on ClinicalTrials.gov