Complication Rate of Onlay vs Sublay Mesh Repair in Incisional Hernia (NCT07401446) | Clinical Trial Compass
CompletedNot Applicable
Complication Rate of Onlay vs Sublay Mesh Repair in Incisional Hernia
Pakistan350 participantsStarted 2020-08-01
Plain-language summary
This randomized controlled trial was conducted at the Department of Surgery, Hayatabad Medical Complex, Peshawar. Eligible patients with incisional hernia were randomized into two parallel groups: sublay mesh repair and onlay mesh repair. Procedures were performed by a single experienced general surgeon. Postoperative complications were assessed by an independent surgeon blinded to the type of procedure. Patients were followed for a period of three months to evaluate safety and recurrence outcomes.
Who can participate
Age range
18 Years – 60 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:
* Adults aged 18-60 years.
* Patients diagnosed with primary incisional hernia on clinical examination.
* Hernia suitable for open surgical repair with mesh.
* Both male and female patients.
* Patients able and willing to provide written informed consent.
Exclusion Criteria:
* Obstructed or strangulated hernia on presentation.
* Recurrent incisional hernia.
* Patients with BMI \> 40.
* Patients with debilitating chronic diseases, including:
* Chronic liver disease
* Chronic renal impairment
* Chronic cardiac disease
* Chronic pulmonary disease
* Patients with American Society of Anesthesiologists (ASA) physical status ≥ 3.
* Patients unfit for general anesthesia.
* Patients unable or unwilling to follow up for postoperative assessment.
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.