← Back to Clinical Trials
Recruiting NCT05920200

NCT05920200 Factors Influencing the Results of Treatment in Patients With Hernias of Various Localizations

◆ AI Clinical Summary
Plain-language summary for patients
Clinical Trial Summary
NCT ID NCT05920200
Status Recruiting
Phase
Sponsor Immanuel Kant Baltic Federal University
Condition Inguinal Hernia
Study Type OBSERVATIONAL
Enrollment 4,000 participants
Start Date 2020-01-09
Primary Completion 2025-12-31

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 90 Years
Study Type OBSERVATIONAL
Interventions
open non-mesh hernia repairopen mesh hernia repairMIS hernia repair

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 4,000 participants in total. It began in 2020-01-09 with a primary completion date of 2025-12-31.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief 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).

Eligibility Criteria

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;

Contact & Investigator

Central Contact

Viktor V Kakotkin, MD

✉ Vkakotkin@kantiana.ru

📞 +74012595071

Frequently Asked Questions

Who can join the NCT05920200 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 90 Years, studying Inguinal Hernia. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05920200 currently recruiting?

Yes, NCT05920200 is actively recruiting participants. Contact the research team at Vkakotkin@kantiana.ru for enrollment information.

Where is the NCT05920200 trial being conducted?

This trial is being conducted at Kaliningrad, Russia.

Who is sponsoring the NCT05920200 clinical trial?

NCT05920200 is sponsored by Immanuel Kant Baltic Federal University. The trial plans to enroll 4,000 participants.

Related Trials

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology