Viewing Study NCT02263612


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Study NCT ID: NCT02263612
Status: COMPLETED
Last Update Posted: 2018-06-27
First Post: 2014-09-20
Is Gene Therapy: True
Has Adverse Events: False

Brief Title: Late Mesh Complications After 3258 Incisional Hernia Operations
Sponsor: Zealand University Hospital
Organization:

Study Overview

Official Title: Late Mesh Complications After 3258 Incisional Hernia Operations
Status: COMPLETED
Status Verified Date: 2018-06
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The Danish Hernia Database (DHD) registers 37 different perioperative parameters. The aim of present study is to use large-scale data from DHD to uncover risk factors for long-term (30 days postoperative and later) readmission, reoperation, death and reoperation for recurrence after incisional hernia repair with use of a synthetic mesh.
Detailed Description: All principal incisional hernias registered in the Danish Hernia Database are included in the study. The included patients have been followed for more than 4 years in order to identify correlation between technical aspects of the hernia repair and postoperative morbidity.

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: