”Postoperative pain treatment with fentanyl patch after forefoot surgery/ Jalkateräleikkauksen jälkeinen kivunhoito kipulaastarilla”.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

EU CTR

Registry ID

EUCTR2008-006000-30-FI

Enrollment

Registered

2008-11-07

Start date

2009-01-09

Completion date

Unknown

Last updated

2014-10-27

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

Conditions

The patients will be recruited from 18-75 year old male or female patients undergoing hallux valgus or hallux rigidus surgery. MedDRA version: 9.1 Level: LLT Classification code 10019095 Term: Hallux Valgus correction MedDRA version: 9.1 Level: LLT Classification code 10019092 Term: Hallux rigidus

Interventions

Trade Name: Durogesic Pharmaceutical Form: INN or Proposed INN: FENTANYL CAS Number: 437387 Pharmaceutical form of the placebo: Transdermal patch Route of administration of the placebo: Transdermal

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Main Objective: ;Secondary Objective: ;Primary end point(s):	—

Countries

Finland

Outcome results

None listed

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