Study of recurrence and complications of inguinal hernia repair

Investigating the rate of recurrence and other complications of inguinal hernia repair with the standard method without and with the use of propylene mesh in a period of one year

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20251001067442N1

Enrollment

Registered

2025-12-14

Start date

2024-12-30

Completion date

Unknown

Last updated

2026-02-02

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

Conditions

Inguinal hernia.

Interventions

Intervention 1: A. Prolene mesh recipient group: After performing the necessary preoperative measures, patients will undergo inguinal hernia repair surgery under anesthesia using the classic method. F

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Age over 18 years old Having a direct hernia with a defect in the posterior wall Being a candidate for classic hernia repair Consent to participate in the study

Exclusion criteria

Exclusion criteria: Having diabetes or bleeding disorders Being treated with aspirin and other anticoagulants or corticosteroids

Design outcomes

Primary

Measure	Time frame
Recurrence of inguinal hernia repair. Timepoint: Re-evaluation 1, 3, 6 and 12 months after surgery. Method of measurement: Data will be collected by clinical examination. And it will be recorded in the attached questionnaire form (presence and absence) and prepared for recording statistical information.;Pain in inguinal hernia repair. Timepoint: Re-evaluation 1, 3, 6 and 12 months after surgery. Method of measurement: Patient rejection is also recorded using the VAS pain questionnaire (attached).;Hematoma after inguinal hernia repair. Timepoint: Re-evaluation 1, 3, 6 and 12 months after surgery. Method of measurement: Data will be collected by clinical examination. And it will be recorded in the attached questionnaire form (presence and absence) and prepared for recording statistical information.;Seroma after inguinal hernia repair. Timepoint: Re-evaluation 1, 3, 6 and 12 months after surgery. Method of measurement: Data will be collected by clinical examination. And it will be recorded in the attached questionnaire form (presence and absence) and prepared for recording statistical information.	—

Measure

Time frame

Recurrence of inguinal hernia repair. Timepoint: Re-evaluation 1, 3, 6 and 12 months after surgery. Method of measurement: Data will be collected by clinical examination. And it will be recorded in the attached questionnaire form (presence and absence) and prepared for recording statistical information.;Pain in inguinal hernia repair. Timepoint: Re-evaluation 1, 3, 6 and 12 months after surgery. Method of measurement: Patient rejection is also recorded using the VAS pain questionnaire (attached).;Hematoma after inguinal hernia repair. Timepoint: Re-evaluation 1, 3, 6 and 12 months after surgery. Method of measurement: Data will be collected by clinical examination. And it will be recorded in the attached questionnaire form (presence and absence) and prepared for recording statistical information.;Seroma after inguinal hernia repair. Timepoint: Re-evaluation 1, 3, 6 and 12 months after surgery. Method of measurement: Data will be collected by clinical examination. And it will be recorded in the attached questionnaire form (presence and absence) and prepared for recording statistical information.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactBorzo Khalidifar

Shahre-kord University of Medical Sciences

Dr.borzookhaledifar@gmail.com+98 38 3226 4837

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 7, 2026