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Clinical study on the changes of polypropylene microparticles in blood after hernial patch implantation

Clinical study on the changes of polypropylene microparticles in blood after hernial patch implantation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200060056
Enrollment
Unknown
Registered
2022-05-16
Start date
2022-05-06
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

abdominal external hernia

Interventions

Abdominal wall hernia repair group:Tension-free repair of external abdominal hernia

Sponsors

The First Affiliated Hospital of Shandong First Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Aged 16-65 years; 2. Patients with external abdominal hernia; 3. Tension-free repair of external abdominal hernia with polypropylene mesh; 4. Agreed to join the research group after explaining the situation to the patients and their families.

Exclusion criteria

Exclusion criteria: 1. Intellectual disability or mental illness; 2. Previous implantation history of polypropylene and other plastic products; 3. Pregnant or lactating patients; 4. Severe complications that cannot tolerate surgery; 5. Participate in conflicting research programmes.

Design outcomes

Primary

MeasureTime frame
Polypropylene microparticle content in blood;

Countries

China

Contacts

Public ContactHu Sanyuan
2532983752@qq.com+86 187658563605

Outcome results

None listed

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