CompletedNot Applicable

Prevention of Postoperative Ventral Hernias

Russia700 participantsStarted 2018-12-12

Plain-language summary

The research is aimed at identifying factors of herniation after median laparotomy and developing surgical methods for preventing postoperative ventral hernias and eventrations.

Who can participate

Age range

18 Years – 90 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Patients of both sexes aged 18 years and older who are expected to perform median laparotomy on a planned or emergency basis.
. Patients who have signed an informed consent to participate in the study, after the purpose and meaning of the study have been explained to them.
. Patients who follow the doctor's instructions.

Exclusion criteria

. The death of the patient.
. Stage IV cancer
. Hernia repair with hernioplasty, including simultaneous surgery
. Refusal of the patient to cooperate with the researcher.

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Wound complications

Timeframe: 2 weeks

Eventration

Timeframe: 2 weeks

Pain syndrome

Timeframe: 2 year

Postoperative ventral hernia

Timeframe: 2 year

Defects in the aponeurosis

Timeframe: 2 year

Trial details

NCT IDNCT04562363

SponsorRyazan State Medical University

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2021-12-12

View on ClinicalTrials.gov More Gangrenous Postoperative Ventral Hernia (Diagnosis) trials

Who can participate

Age range

18 Years – 90 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

. Patients of both sexes aged 18 years and older who are expected to perform median laparotomy on a planned or emergency basis.
. Patients who have signed an informed consent to participate in the study, after the purpose and meaning of the study have been explained to them.
. Patients who follow the doctor's instructions.

Exclusion criteria

. The death of the patient.
. Stage IV cancer
. Hernia repair with hernioplasty, including simultaneous surgery
. Refusal of the patient to cooperate with the researcher.