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Quality of life after inguinal hernia repair

Quality of life After Inguinal Hernia Repair: progrip vs prolene a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN21578845
Enrollment
200
Registered
2017-12-23
Start date
2017-01-01
Completion date
Unknown
Last updated
2018-01-15

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

Conditions

Inguinal hernia Injury, Occupational Diseases, Poisoning Inguinal hernia

Interventions

Five consultants from the Surgical Department of “Agios Dimitrios Hospital” participated in the study, operated one patient at a time consequently, with both techniques, according to the randomization

Sponsors

Agios Dimitrios General Hospital scientific committee
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Male patients with inguinal hernia, fit to surgery. 2. Aged 18-75 years old

Exclusion criteria

Exclusion criteria: 1. Relapse 2. Bilateral inguinal hernia 3. Strangulated inguinal hernia 4. Female patients 5. Inguinoscrotal hernia 6. Laparoscopic repair 7. Other alongside surgery

Design outcomes

Primary

MeasureTime frame
1. Pain in measured using the Visual Analogue Scale Core (VAS) at one and six months 2. Quality of life is mesaured using the questionnaire SF36 at one and six months

Secondary

MeasureTime frame
Immediate and long-term postoperative complications are measured using the medical records when they occur and at six months.

Countries

Greece

Outcome results

None listed

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