Fewer stitches, less pain? new hernia fix shows promise
NCT ID NCT07334548
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether using only three fixation points for mesh in hernia repair reduces pain and complications compared to the standard method. Sixty-four adults with inguinal hernia were randomly assigned to one of the two techniques. The goal is to see if a less invasive fixation can improve recovery without raising the risk of hernia recurrence.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- polypropylene mesh
- What this could lead to
- If successful, this simpler fixation method could reduce pain and complications after hernia surgery without increasing the risk of hernia recurrence.
- What could go wrong
- This is a small, single-center trial with only 64 participants, so results may not apply widely. The new technique might not significantly improve outcomes or could lead to higher recurrence rates.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
64 people
The number who actually took part.
- Started
-
Sep 2025
- Finished
-
Feb 2026
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 70 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: Patients presenting to the outpatient department with unilateral inguinal hernia requiring Lichtenstein repair Age between 18-70 years Both male and female ASA I-II Exclusion Criteria: Recurrent, bilateral, complicated, or incisional hernia Patients with pre-existing obstructive LUTS Chronic kidney disease (CKD), patients on hemodyalysis. Chronic liver disease (CLD)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Sindh Institute of Urology and Transplantation
Karachi, Sindh, 74200, Pakistan
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