CTRI/2009/091/000056
Completed
Phase 3
A comparative clinical trial for the evaluation of the efficacy and safety of FDC of Lornoxicam (4 mg) and Paracetamol (500 mg)with Lornoxicam (4 mg) alone for short term treatment of mild to moderate pain associated with extra articular inflammation
Aristo Pharmaceuticals pvt ltd Mumbai0 sites201 target enrollmentTBD
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Aristo Pharmaceuticals pvt ltd Mumbai
- Enrollment
- 201
- Status
- Completed
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Patients with either sex, from 18\-60 years age. Informed consent, extra articular inflammation.
Exclusion Criteria
- •Female pregnant or with chances of pregnancy or nursing, History of allergy or hypersensitivity. physical/clinical abnormalities, any condition which affect study of drug.
Outcomes
Primary Outcomes
Not specified
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