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Comparison of Self Fixating Mesh to Mesh Fixation With Metallic Tacks in Laparoscopic Inguinal Hernia Repair

Unknown statusNot applicableNCT03564535
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

This study compares the use of self-fixating mesh to mesh fixation with tackers in the management of inguinal hernia by laparoscopic method. Half of the participants in the study will be treated using self-fixating mesh, while the other half will be treated using conventional mesh fixed with tackers.

Study details

Official title
Comparison of Mesh Fixation With Tackers to Use of Self Fixating Mesh in Total Extra Peritoneal Inguinal Hernia Repair: A Double Blinded Randomized Controlled Trial
Conditions
Interventions
  • Device: Self fixating group
  • Device: Tacker fixation group
Sponsor
All India Institute of Medical Sciences, Bhubaneswar
Start date
2018-04-18
Primary completion
2021-03
Sex
All
Age range
from 18 Years to 80 Years
Results posted
No results posted in this snapshot
Countries
India
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: 1. Unilateral inguinal hernia 2. Age 18-80years 3. American Society of Anesthesiologists (ASA) Grade 1 or 2 Exclusion Criteria: 1. Patient unfit for general anesthesia or laparoscopic surgery 2. Large scrotal hernias 3. Irreducible hernias 4. Morbid obesity 5. Previous pelvic surgery 6. Coagulopathy 7. Those who cannot understand the VAS score 8. Those who did not agree to participate in the study 9. Gastritis 10. Gastroesophageal reflux disease 11. Liver dysfunction 12. kidney dysfunction

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT03564535