Late Mesh Complications After 3258 Incisional Hernia Operations

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02263612

Enrollment

3258

Registered

2014-10-13

Start date

2007-01-31

Completion date

2015-09-30

Last updated

2018-06-27

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

Conditions

Incisional Hernia

Keywords

Incisional Hernia, Complications, Long-term

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.

Interventions

None listed

Study design

Observational model

COHORT

Time perspective

RETROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

Yes

Inclusion criteria

* Incisional Hernia Repair

Design outcomes

Primary

Measure	Time frame	Description
Reoperation	Up to 7 years	Riskfactors for reoperation (any procedure) more than 30 days after incisional hernia repair

Secondary

Measure	Time frame	Description
Readmission	Up to 7 years	Riskfactors for readmission later than 30 days after incisional hernia repair

Other

Measure	Time frame	Description
Death	Up to 7 years	Riskfactors for death later than 30 days after incisional hernia repair

Countries

Denmark

Outcome results