Completed
High Agreement Between the Danish Ventral Hernia Database and Hospital Files in Region Zealand
What is being collected
Procedure Data
Collected from past medical records and data - RetrospectiveProcedure
Who is being recruted
From 18 to 120 Years
1 Eligibility Criteria
How is the trial designed
Cohort
Tracking disease incidence in order to identify risk factors and understand disease progression over time.Observational
Study Start: October 2010
Summary
Principal SponsorZealand University Hospital
Last updated: July 13, 2023
Sourced from a government-validated database.Claim as a partner
Study start date: October 1, 2010
Actual date on which the first participant was enrolled.Is there agreement between data in the Danish Ventral Hernia Database and patient files
Principal SponsorZealand University Hospital
Last updated: July 13, 2023
Sourced from a government-validated database.Claim as a partner
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.Design Details
408 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Cohort
These studies follow a group of individuals with common characteristics (such as a condition or birth year) over a specific period to study health outcomes or exposures.
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.Criteria
Any sex
Biological sex of participants that are eligible to enroll.From 18 to 120 Years
Range of ages for which participants are eligible to join.Healthy volunteers not allowed
If individuals who are healthy and do not have the condition being studied can participate.Criteria
1 inclusion criteria required to participate
All ventral hernia repairs
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.Treatment Groups
Study Objectives
One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Study Objectives
Primary Objectives
Study Centers
These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.This study has 1 location
CompletedOne Study Center