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Optimisation of incision hernia surgery treatment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN45000842
Enrollment
150
Registered
2008-03-04
Start date
2007-07-01
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

Hernia Digestive System Hernia

Interventions

Three groups: 1. Keel technique 2. Onlay technique 3. Sublay technique The follow up period is 2 weeks, 1, 3, 6 and 12 months after surgery. Surgery, blood gas analysis and intra-abdominal pressure i

Sponsors

Kaunas Medical University Hospital (Lithuania) - Department of Surgery
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All 18 - 80 years old patients with incision hernia, who will be operated and agree to participate in this clinical trial.

Exclusion criteria

Exclusion criteria: 1. Patients older than 80 years 2. Incarcerated incision hernia 3. Mental patients with incision hernia 4. Pregnant women with incision hernia 5. Patients with incision hernia do not agree to participate in this clinical trial

Design outcomes

Primary

MeasureTime frame
1. Recurrence rate, measured at 2 weeks, 1, 3, 6 and 12 months after surgery 2. Quality of life, measured using the 36-item Short Form health survey version 2 (SF-36 v2)at 2 weeks, 1, 3, 6 and 12 months after surgery

Secondary

MeasureTime frame
1. Postoperative complications, measured at 2 weeks, 1, 3, 6 and 12 months after surgery 2. Change of the blood gas and intra-abdominal pressure, measured before and after surgery 3. Recovering time to the normal physical activity after surgery, measured at 2 weeks, 1, 3, 6 and 12 months after surgery

Countries

Lithuania

Outcome results

None listed

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