Efficacy of perioperative duloxetine in patients at high risk for developing chronic postsurgical pain after inguinal hernia repair: a multicenter randomized controlled trial

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

EU CTIS

Registry ID

CTIS2023-505860-12-00

Acronym

ICI21/00006l

Enrollment

294

Registered

2023-09-15

Start date

2024-06-26

Completion date

Unknown

Last updated

2025-04-25

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

Conditions

Chronic postsurgical pain after inguinal hernia repair

Brief summary

Incidence of CSPS (Chronic post-surgical pain) at 4 months

Detailed description

Quality of life by means of questionnaire SF-12, Rate of adverse events perioperatively

Interventions

DRUGCapsules of maltodextrine

DRUGDulotex 30 mg cápsulas duras gastrorresistentes EFG

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Design outcomes

Primary

Measure	Time frame
Incidence of CSPS (Chronic post-surgical pain) at 4 months	—

Secondary

Measure	Time frame
Quality of life by means of questionnaire SF-12, Rate of adverse events perioperatively	—

Countries

Spain

Outcome results

None listed

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