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Different methods of mesh fixation in hernia surgery: a comparision of post operative outcomes

Comparing Sutures vs. N-hexyl cyanoacrylate glue mesh fixation in reducing postoperative pain in patients undergoing unilateral inguinal hernia repair-A single blinded randomized control trail - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/04/084850
Enrollment
80
Registered
2025-04-15
Start date
Unknown
Completion date
Unknown
Last updated
2025-04-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Comparing sutures vs. n-hexyl-cyanoacrylate glue mesh fixation in reducing pain in post operative period: NOT APPLICABLE Intervention2: n-hexyl-cyanoacrylate glue: mesh fixation will be

Sponsors

JIPMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All consenting patients with primary elective unilateral uncomplicated inguinal hernia planned for open mesh repair

Exclusion criteria

Exclusion criteria: 1.Hernia patients with disorders of hemostasis and coagulation 2.Chronic pain due to previously operated opposite side or due to any other medical problem 3.Patient undergoing concomitant surgeries along with mesh repair

Design outcomes

Primary

MeasureTime frame
To assess the efficacy of sutures vs. N-hexyl-cyanoacrylate for mesh fixation in reducing postoperative pain during elective primary unilateral inguinal hernia repair.fixation in reducing postoperative pain during elective primary unilateral inguinal hernia repair.Timepoint: day 0,1,2,7,30 of surgery

Secondary

MeasureTime frame
1. To compare the short-term outcomes (local numb-ness & hematoma, seroma, rate of SSI, urinary reten-tion, length of operation, intraoperative time for mesh fixation, Length of hospital stay & time to return to work) between the two groups 2. To compare the long-term outcomes (Chronic pain, & recurrence) between the two groups Timepoint: day 0,1,2,7,30, after 6 months & 1year of surgery

Countries

India

Contacts

Public ContactVijaykumar C

JIPMER

johnsonmichael831537@gmail.com09100831537

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026