Abdominal Hernia Clinical Trial
Official title:
Long Term Outcomes Following Hernia Repair With Mesh
NCT number | NCT04578340 |
Other study ID # | EH20-388 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | October 1, 2020 |
Est. completion date | October 1, 2026 |
Verified date | November 2023 |
Source | NorthShore University HealthSystem |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational [Patient Registry] |
The objective of this study is to establish the extent to which mesh improves quality of life and surgical outcomes following hernia repair.
Status | Recruiting |
Enrollment | 4700 |
Est. completion date | October 1, 2026 |
Est. primary completion date | October 1, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - abdominal hernia repair using mesh Exclusion Criteria: - less than 18 years old |
Country | Name | City | State |
---|---|---|---|
United States | NorthShore University HealthSystem | Evanston | Illinois |
Lead Sponsor | Collaborator |
---|---|
NorthShore University HealthSystem | Medtronic |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Hernia recurrence rate | Should the hernia repair fail and the hernia reappears, this is counted as a recurrent hernia. | Within 5 years of initial hernia repair | |
Primary | Patient quality of life | Quality of life before and after surgery will be compared using various self-reported assessment tools/questionnaires. | Up to 5 years postopertively | |
Secondary | Postoperative infection rate | Infection related to hernia repair or mesh use will be reported. | Up to 5 years postoperatively |
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