Not yet recruiting NCT07210424
Comparative Study on the Post-operative Pain and Other Outcomes of Mesh Fixation With Prolene vs Vicryl vs Skin Staples in Lichtenstein Inguinal Hernia Repair.
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Mesh Fixation.
- Who it may be relevant to
- Registry conditions: Inguinal Hernia. Basic parameters: 18 years — 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Overview
We are going to see the outcome measures for patient and compare them across two groups, those who are undergoing mesh fixation for inguinal hernia by sutures, and those who are fixated by skin staples.
Interventions
- Procedure Mesh Fixation
Mesh fixation during Lichtenstein inguinal hernia repair.
Primary outcome measures
- Post Operative Pain [Time frame: At 3, 7, 14 and 30 post op day]
Eligibility criteria
Inclusion criteria
- Patients undergoing inguinal hernia repair
- 18-65 years
- Both genders
Exclusion criteria
- COPD
- Immunocompromised
- Obstructive Uropathy
- Chronic constipation
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07210424 · 511/RC/KEMU