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OpenTrials
Completed

NCT Number: NCT02263625

Regional Differences In Indication for Ventral Hernia Repair

The aim of the present study is to investigate whether there are differences in indication for ventral hernia repair and surgical approach among hernia surgeons from different geographical regions of Denmark.

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Køge Sygehus

Køge, 4600, Denmark

About this study

30 outpatient consultation will be taped and distributed among hernia surgeons in different regions of Denmark. The surgeon will then be asked to answer a questionnaire regarding the treatment and surgical technique.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients referred to Køge Hospital Surg. Department with ventral hernia in December 2014

Treatment and study plan

Primary outcomes

  1. Differences in indication for ventral hernia repair

    Time frame: 6 months

    Number of patients offered a ventral hernia repair after primary consultation by different hernia specialists.

Secondary outcomes

  1. Differences in choice of surgical technique between surgeons

    Time frame: 6 months

    Which surgical approach does different surgeons offer patients with a ventral hernia

Sponsors and collaborators

Lead sponsor

Zealand University Hospital

Other

Registry information

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Oct 13, 2014
Registry last updated
Jun 27, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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