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A clinical trial to assess the effectiveness of paracetamol Immediate Release tablets in patients with fever.

Phase 4
Completed
Conditions
Health Condition 1: null- Patients having fever at least 38 degrees celsius or 100.4 degrees Fahrenheit
Registration Number
CTRI/2011/03/001653
Lead Sponsor
Panacea Biotec Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
110
Inclusion Criteria

1.Patients of either sex, 18-65years

2.Patients having fever at least 380C or 100.40F

3.Patients willing to give informed consent

4.Patients able to take oral medications

Exclusion Criteria

1.Subjects requiring hospitalization

2.Subjects with known or suspected hypersensitivity to paracetamol or any the constituents of the formulation.

3.Subjects who have received any other investigational drug within 1 month prior to screening or enrollment.

4.Subjects who have received Paracetamol or any NSAID within 6 hours prior to enrollment.

5.Subjects who are receiving other medications or who have disease conditions that could interfere with the evaluation of drug efficacy or drug safety.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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