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Study protocol for a randomised clinical trial comparing TREPP versus Lichtenstein*s technique in Inguinal hernia patients

Study protocol for a randomised clinical trial comparing TREPP versus Lichtenstein*s technique in Inguinal hernia patients - TREPPoLi Trial

Status
Unknown
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON45767
Enrollment
750
Registered
2018-12-17
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

Inguinal hernia

Interventions

TREPP or Lichtenstein

Sponsors

Medisch Centrum Leeuwarden
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Adults with a clinically apparent primary unilateral inguinal hernia Age > 18 years ASA classification 1-3 Signed informed consent

Exclusion criteria

Exclusion criteria: Recurrent inguinal hernia bilateral inguinal hernia ASA class 4 Acute incarcerated inguinal hernia psychiatric disease or other reasons making follow-up or questionnaires unreliable previous preperitoneal surgery (e.g. radical prostatectomy)

Design outcomes

Primary

MeasureTime frame
Chronic postoperative inguinal pain—

Secondary

MeasureTime frame
Secondary outcomes are complications, recurrences, sexual complaints, bleeding, time of return to daily activities and operating time.—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)