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

Conditions
The patients will be recruited from 18-75 year old male or female patients undergoing hallux valgus or hallux rigidus surgery.
MedDRA version: 9.1Level: LLTClassification code 10019095Term: Hallux Valgus correction
MedDRA version: 9.1Level: LLTClassification code 10019092Term: Hallux rigidus
Registration Number
EUCTR2008-006000-30-FI
Lead Sponsor
Riika Merivirta
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
60
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

Not provided

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Main Objective: ;Secondary Objective: ;Primary end point(s):
Secondary Outcome Measures
NameTimeMethod
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