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A randomized controlled study on the application of biological mesh and polypropylene mesh in inguinal hernia repair

A randomized controlled study on the application of biological mesh and polypropylene mesh in inguinal hernia repair

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070222
Enrollment
Unknown
Registered
2023-04-06
Start date
2023-04-10
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

inguinal hernia

Interventions

Test group:Biological mesh used
Control group:polypropylene mesh used

Sponsors

The First Affiliated Hospital of Zhengzhou University
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Male; Age >= 18 years old; Primary unilateral inguinal hernia; ASA grade I-III.

Exclusion criteria

Exclusion criteria: Incarcerated hernia or strangulated hernia.

Design outcomes

Primary

MeasureTime frame
Recurrence;—

Secondary

MeasureTime frame
Pain;Quality of Life;—

Countries

China

Contacts

Public ContactWang Dianchen

The First Affiliated Hospital of Zhengzhou University

wdc8681949@163.com+86 371 6796 7277

Outcome results

None listed

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