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Comparison of the effect of fix and non-fix mesh (Use of external fixation (hernia band) after surgery) in causing complications after hernioplasty surgery

Comparative study of the effect of fixation mesh and non-fixation of mesh (Use of external fixation (hernia band) after surgery) in causing postoperative complications in patients with inguinal hernia undergoing laparoscopic hernioplasty

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200825048515N25
Enrollment
64
Registered
2021-03-17
Start date
2021-02-07
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

Inguinal hernia. Unilateral inguinal hernia, with obstruction, without gangrene

Interventions

Intervention 1: Control group: Patients in this group are treated for inguinal hernia repair by laparoscopic method and for these patients the mesh(Bard 3D Max) is fixed internally (using Vicryl sutur

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Having an inguinal hernia Satisfaction with participation in this study

Exclusion criteria

Exclusion criteria: Having an incarcerated hernia Having a strangulated hernia Having a very large inguinal hernia (scrotal) Having a femoral inguinal hernia

Design outcomes

Primary

MeasureTime frame
Seroma. Timepoint: 1, 3 and 6 months after surgery. Method of measurement: Observation.;Hematoma. Timepoint: 1, 3 and 6 months after surgery. Method of measurement: Observation.;Pain. Timepoint: 1, 3 and 6 months after surgery. Method of measurement: Visual Analogue Scale (VAS).

Secondary

MeasureTime frame
Recurrence of hernia. Timepoint: 1, 3 and 6 months after surgery. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasoud Sayadi Shahraki

Esfahan University of Medical Sciences

sayadi@med.mui.ac.ir+98 31 3620 2020

Outcome results

None listed

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