Effect of oblique external flap and mesh on inguinal hernia's patients

Comparison of the complications of oblique external flap procedure and mesh for the repair of the channel in inguinal hernia's patients

Status

Recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20211129053215N1

Enrollment

Registered

2022-03-07

Start date

2022-02-11

Completion date

Unknown

Last updated

2022-04-04

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

Conditions

Inguinal hernia. Inguinal hernia

Interventions

Intervention 1: Intervention group 1: In this intervention, patients with loose inguinal canal floor will be repaired using the oblique external flap. Intervention 2: Intervention group 2: In this int

Eligibility

Sex/Gender

Male

Inclusion criteria

Inclusion criteria: Patients with a straight inguinal hernia with a loose canal floor

Exclusion criteria

Exclusion criteria: Patients with a history of inguinal hernia surgery Elderly people with weak external oblique fascia Patients with a history of mesh implantation

Design outcomes

Primary

Measure	Time frame
Pain. Timepoint: One day after surgery, 6 months after surgery, 12 months after surgery. Method of measurement: Interview with the patient.	—

Secondary

Measure	Time frame
Recurrence of hernia. Timepoint: 6 months after surgery, 12 months after surgery. Method of measurement: Perform ultrasound.;Infection of surgery site. Timepoint: 6 months after surgery, 12 months after surgery. Method of measurement: Ultrasound.;Post operative hematoma. Timepoint: During the week after surgery. Method of measurement: Perform ultrasound.;Feeling of a foreign body at the operation site. Timepoint: Post operative surgery. Method of measurement: Interview with the patient.	—

Measure

Time frame

Recurrence of hernia. Timepoint: 6 months after surgery, 12 months after surgery. Method of measurement: Perform ultrasound.;Infection of surgery site. Timepoint: 6 months after surgery, 12 months after surgery. Method of measurement: Ultrasound.;Post operative hematoma. Timepoint: During the week after surgery. Method of measurement: Perform ultrasound.;Feeling of a foreign body at the operation site. Timepoint: Post operative surgery. Method of measurement: Interview with the patient.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactElham Jahantabi

Tabriz University of Medical Sciences

zomorrodiaf@gmail.com+98 41 3334 7054

Outcome results

None listed

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