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 range18 Years – 90 Years

SexALL

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.

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