Factors Influencing the Results of Treatment in Patients With Hernias of Various Localizations

ConditionsInguinal Hernia Femoral Hernia Umbilical Hernia Ventral Hernia Chronic Pain Acute Post Operative Pain Recrrence Rate

Trial statusRecruiting

Trial phaseNot listed

Trial typeObservational

Biological sexAll

Age18-90

SponsorImmanuel Kant Baltic Federal University

About this trial

The study attempts to quantify the relative risks for acute postoperative pain, complications rate, chronic postoperative pain (CPIP) and recurrence rate after different methods of repair of groin, umbilical and incisional hernia depending on surgical technique, mesh type and fixation suture material.

For this purpose the investigators will analyze data from the Kalinigrad Hernia Registry (KHR).

Eligibility criteria

Qualifiers

All mesh and non-mesh repairs that have been registered in the KHR from January 9, 2020, until December 31, 2023.

Disqualifiers

Patients not having a 11-digit state-assigned Personal insurance policy number.

Parastomal hernia;

infected hernias;

Trial design

Treatments tested in this trial

open non-mesh hernia repair
open mesh hernia repair
MIS hernia repair

Treatment groups

4,000 Participants

are divided into 3 treatment groups

Sponsors and collaborators

Immanuel Kant Baltic Federal University

Lead sponsor

Source ClinicalTrials.gov