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Multi-center prospective cohort study of national innovative medical device composite hernia patch

Multi-center prospective cohort study of national innovative medical device composite hernia patch

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000030197
Enrollment
Unknown
Registered
2020-02-25
Start date
2020-03-01
Completion date
Unknown
Last updated
2020-03-02

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

Conditions

Inguinal Hernia

Interventions

Case series:Inguinal hernia repair with patch

Sponsors

Shanghai Pine&Power Biotech Co.,Ltd
Lead Sponsor

Eligibility

Sex/Gender
All
Age
14 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Patients with inguinal hernia, aged over 14 years; 2. Patients whose informed consent is signed by the patient or his guardian after informed in detail by the doctor of the clinical trial.

Exclusion criteria

Exclusion criteria: 1. Any situation that affects the correct evaluation of pain (uncooperatives or drug addicts or mental illness patients); 2. Allergic to the test materials; 3. Patients who are not considered suitable for study by clinical evaluation; 4. Patients who do not agree with the group or could not cooperate to complete the follow-up.

Design outcomes

Primary

MeasureTime frame
Postoperative chronic pain (VAS score);

Secondary

MeasureTime frame
Inguinal hernia pain questionnaire ;Inguinal hernia Sexual function scale;recurrence rate;complications including postoperative infection, seroma, local foreign body sensation, etc.;

Countries

China

Contacts

Public ContactJianxiong Tang

East China Hospital Affiliated to Fudan University

johnxiong@china.com+86 13901791469

Outcome results

None listed

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