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(PREVENT)A Randomized, Double-blind, Placebo-controlled Trial on the Prevention of Chronic Postoperative Pain after Inguinal Hernia and Knee Surgery by Postoperative Treatment with Tapentadol

Status
Not yet recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-511010-21-00
Enrollment
540
Registered
2024-07-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

chronic postoperative pain

Brief summary

The effect of Tapentadol compared to placebo on the development of chronic pain in the first year after surgery in patients planned for elective inguinal hernia surgery and knee replacement surgery.

Interventions

DRUGPALEXIA Retard 50 mg tabletten met verlengde afgifte

Sponsors

Leids Universitair Medisch Centrum (LUMC)
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
The effect of Tapentadol compared to placebo on the development of chronic pain in the first year after surgery in patients planned for elective inguinal hernia surgery and knee replacement surgery.

Countries

Netherlands

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026