Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05750368
Other study ID # women-epigastric
Secondary ID
Status Completed
Phase
First received
Last updated
Start date September 1, 2022
Est. completion date February 1, 2023

Study information

Verified date March 2023
Source Bispebjerg Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim was to evaluate outcomes after epigastric hernia repair in women on a nationwide basis. The primary outcome iss recurrence - secondary outcomes are readmission, operation for complication, risk factors for recurrence, and readmittance.


Description:

Aim Outcomes after epigastric hernia repair are rarely reported independently. Furthermore, women have the highest prevalence of epigastric hernia repair in the age of 41-50 years. The aim of this study was to evaluate long-term outcomes after epigastric hernia repairs in women on a nationwide basis. Methods Nationwide database cohort study using prospectively recorded data from the Danish Hernia Database from women undergoing elective repair for epigastric hernias, during a 4-year period (2018-2021). A 100% follow-up was obtained by combining intra-operative data with data from the National Civil Register (NRC). The primary outcome was operation for recurrence, secondary outcomes were readmission and operation for complications. We compared open vs. laparoscopic repairs, and subgroup analysis were made for open repairs (sutured vs. mesh).


Recruitment information / eligibility

Status Completed
Enrollment 3031
Est. completion date February 1, 2023
Est. primary completion date January 1, 2023
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 120 Years
Eligibility Inclusion Criteria: - All female patients undergoing elective repair with a laparoscopic or open technique for an epigastric hernia were included. Exclusion Criteria: - umbilical or incisional hernias, male patients, recurrent hernia repairs, and hernia repairs performed in relation to other surgical procedures.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
Denmark Bispebjerg Hospital Copenhagen

Sponsors (2)

Lead Sponsor Collaborator
Bispebjerg Hospital Herlev Hospital

Country where clinical trial is conducted

Denmark, 

Outcome

Type Measure Description Time frame Safety issue
Primary operation for recurrence operation for recurrence during the observation period 4 year
Secondary Readmittance readmittance within 90 days after repair 90 days
Secondary operation for complications 90 days operation for complications 90 days
See also
  Status Clinical Trial Phase
Recruiting NCT06092073 - Bilateral Recto-Intercostal Fascial Plane Block in Epigastric Hernia Repair N/A
Completed NCT04150796 - Comparing eTEP and Laparoscopic Intraperitoneal Onlay Mesh (IPOM) for Ventral Hernias N/A
Completed NCT06115941 - Using Pre-op Incentive Spirometer Reduces Chances of Basal Atelectasis in Patients Undergoing Upper Abdominal Surgeries N/A
Active, not recruiting NCT01761708 - Case-control Study of Mesh-infection After a Size Tailored Hernia Repair With C-Qur V-Patch N/A
Terminated NCT01639118 - Prospective Study Of A Size Tailored Approach To Repair Umbilical And Epigastric Primary Ventral Hernias N/A
Completed NCT01665859 - Risk Factors for Poor Outcome After Epigastric and Umbilical Hernia Repair
Completed NCT06074146 - Outcomes After Epigastric Hernia Repair in Women.