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

NCT05920200 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 4000

Last updated 2024-07-23

No results posted yet for this study

Summary

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).

Conditions

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

Interventions

PROCEDURE

open non-mesh hernia repair

A groin and femoral hernia non-mesh repair. An umbilical hernia non-mesh repair. A ventral and incisional hernia non-mesh repair.

PROCEDURE

open mesh hernia repair

A groin and femoral hernia repair, reinforced by synthetic mesh. The mesh is affixed with sutures for Lichtenstein. Self-fixating mesh is also possible. An umbilical, ventral, incisional hernia repair, reinforced by synthetic mesh. The mesh is affixed with sutures.

PROCEDURE

MIS hernia repair

A groin and femoral minimal invasive hernia repair (TAPP, eTEP). The mesh is affixed with tack/no-fixation. Self-fixation mesh is also possible. An umbilical, ventral, incisional minimal invasive hernia repair (eTEP, IPOM,). The mesh is affixed with tack and no-fixation .

Sponsors & Collaborators

  • Immanuel Kant Baltic Federal University

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
90 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-01-09
Primary Completion
2025-12-31
Completion
2025-12-31

Countries

  • Russia

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05920200 on ClinicalTrials.gov