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Lichtenstein technique versus transinguinal preperitoneal mesh prosthesis (TIPP): less chronic pain?

The Tilburg double-blind randomised controlled trial comparing inguinal hernia repair according to Lichtenstein and the transinguinal preperitoneal technique

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN93798494
Enrollment
300
Registered
2008-12-23
Start date
2008-12-01
Completion date
Unknown
Last updated
2015-01-13

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

Conditions

Unilateral groin hernia Digestive System Inguinal hernia

Interventions

All patients will be operated via anterior approach with a skin incision two centimetres above the Poupart ligament. In half of the study population the groin hernia will be corrected according to t
a soft mesh will be used instead of the polypropylene mesh. The other 150 inguinal hernia patients will be operated by the transinguinal preperitoneal (TIPP) technique with Polysoft® mesh. In this te

Sponsors

St Elisabeth Hospital (Netherlands)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Primary unilateral groin hernia 2. Aged greater than 18 years, either sex 3. American Society of Anaesthesiologists (ASA) classification 1 - 3 4. Signed informed consent letter

Exclusion criteria

Exclusion criteria: 1. Recurrent hernia 2. Aged less than 18 or greater than 80 years 3. Scrotal hernia(s) 4. ASA classification greater than 4 5. Acute incarcerated inguinal hernia(s) 6. Psychiatric disease or other reason making follow-up or questionnaires unreliable

Design outcomes

Primary

MeasureTime frame
Direct post-operative and chronic pain, measured post-operatively during hospital admission and at 14 days/3 months and one year; final measurement will be after follow up completion of the last patient in both groups.

Secondary

MeasureTime frame
1. Operation time 2. Post-operative complications 3. Hospital stay 4. Return to daily activities (e.g. work) 5. Recurrence Measured post-operatively during hospital admission and at 14 days/3 months and one year; final measurement will be after follow up completion of the last patient in both groups.

Countries

Netherlands

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 25, 2026