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The Use of Bio-Mesh and Polypropylene Mesh in Laparoscopic Inguinal Hernia Repair: A Multi-Center Prospective Cohort Study

The Use of Bio-Mesh and Polypropylene Mesh in Laparoscopic Inguinal Hernia Repair: A Multi-Center Prospective Cohort Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400087392
Enrollment
Unknown
Registered
2024-07-26
Start date
2024-08-01
Completion date
Unknown
Last updated
2024-07-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Inguinal Hernia

Interventions

Polypropylene mesh group:Polypropylene mesh
Bio-mesh group:Bio-Mesh

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged = 18 years old, regardless of gender; 2. With clinical diagnosis of inguinal hernia and planned to undergo laparoscopic inguinal hernia repair; 3. Hernia ring diameter = 2 cm; 4. Voluntarily participate in this study, can follow up as required, and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Those who cannot accept porcine devices due to religious, ethnic or other issues; 2. Those who are considered unsuitable for this clinical study by the researcher.

Design outcomes

Primary

MeasureTime frame
Recurrence-free rate;—

Secondary

MeasureTime frame
Surgical success rate;Recurrence-free rate;Complications;Evaluation of device usage;—

Countries

China

Contacts

Public ContactJinghui Lu

Qilu Hospital of Shandong University

201262005933@email.sdu.edu.cn+86 185 6008 5287

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026