Long Term Outcomes Following Hernia Repair With Mesh

ClinicalTrials.gov ID: NCT04578340

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Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The objective of this study is to establish the extent to which mesh improves quality of life and surgical outcomes following hernia repair.

Study identification

NCT ID: NCT04578340
Recruitment status: Not listed
Study type: Observational
Phase: Not listed
Lead sponsor: Endeavor Health; Other
Enrollment: 4,700 participants

Conditions and interventions

Conditions

Abdominal Hernia

Interventions

Not listed

Eligibility (public fields only)

Age range: 18 Years and older
Sex: All
Healthy volunteers: Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date: Oct 1, 2020 (Actual)
Primary completion: Oct 1, 2025 (Estimated)
Completion: Oct 1, 2026 (Estimated)
Last update posted: Nov 14, 2023

2020 – 2026

United States locations

U.S. sites: 1
U.S. states: 1
U.S. cities: 1

Facility	City	State	ZIP	Site status
NorthShore University HealthSystem	Evanston	Illinois	60201	Recruiting

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows: Public field values for ClinicalTrials.gov record NCT04578340, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do: No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from: Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh: Last update posted Nov 14, 2023 · Synced Nov 15, 2026