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

I

Immanuel Kant Baltic Federal University

Status

Enrolling

Conditions

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

Treatments

Procedure: MIS hernia repair
Procedure: open mesh hernia repair
Procedure: open non-mesh hernia repair

Study type

Observational

Funder types

Other

Identifiers

NCT05920200
HR202339

Details and patient eligibility

About

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).

Enrollment

4,000 estimated patients

Sex

All

Ages

18 to 90 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  • Patients not having a 11-digit state-assigned Personal insurance policy number.
  • Parastomal hernia;
  • infected hernias;

Trial design

4,000 participants in 3 patient groups

Patients with groin and femoral hernia/IG
Treatment:
Procedure: open non-mesh hernia repair
Procedure: open mesh hernia repair
Procedure: MIS hernia repair
Patients with umbilical hernia/IG
Treatment:
Procedure: open non-mesh hernia repair
Procedure: open mesh hernia repair
Procedure: MIS hernia repair
Patients with ventral and incisional hernia/InG
Treatment:
Procedure: open non-mesh hernia repair
Procedure: open mesh hernia repair
Procedure: MIS hernia repair

Trial contacts and locations

1

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Central trial contact

Viktor V Kakotkin, MD

Data sourced from clinicaltrials.gov

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