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NCT06102551

A Retrospective Analysis of Incisional Hernia Repair's Postoperative Recurrence

Completed Last updated 26 October 2023
What this trial tests

trial testing Recurrence after surgery in Incisional Hernia in 157 participants. Completed in 31 August 2023.

Timeline
1 March 2023
Primary endpoint
1 July 2023
31 August 2023

Quick facts

Lead sponsorFudan University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment157
Start date1 March 2023
Primary completion1 July 2023
Estimated completion31 August 2023
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Fudan University

Who can join

Adults 18 to 80, any sex, with Incisional Hernia or Recurrent Hernia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

ABSTRACT Purpose:A retrospective study was conducted among patients with incisional hernia in our hospital to analyse the factors associated with postoperative recurrence of abdominal wall incisional hernia. Methods:Patients with a diagnosis of incisional hernia obtained from our hospital's electronic medical record system were divided into primary incisional hernia group and recurrent incisional hernia group according to whether or not they had a recurrence after surgery. Baseline information on these patients was recorded and statistically analysed after our review.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Incisional Hernia

Currently open trials in the same condition.

Other Fudan University trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06102551.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing