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A randomized study comparing etoricoxib and diclofenac sodium in post hallux valgus surgery pai

Phase 1
Conditions
Postoperative pain
MedDRA version: 12.1Level: PTClassification code 10056350Term: Pain management
Registration Number
EUCTR2010-020547-13-SE
Lead Sponsor
Foot and Ankle Surgical center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
All
Target Recruitment
200
Inclusion Criteria

Patient 18 - 70 years undergoing elective hallux valgus surgery
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) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

NSAID allergy
sever/uncontrolled cardiovascular disease
severe renal or hepatic disease

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Main Objective: Study patients assessment of globbal satisfaction with pain medicatiion;Secondary Objective: Pain, ;Primary end point(s): Patients Global Evaluation of Study Medication
Secondary Outcome Measures
NameTimeMethod
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