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Comparative Bio availability of diclofenac sodium 75 mg per 1 ml injection as intravenous bolus in fasting human volunteers

Not Applicable
Registration Number
CTRI/2019/04/018583
Lead Sponsor
Troikaa Pharmaceuticals Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1 Body Mass Index between 18.5-30 Kg / m2 extremes included

2 Subjects with normal findings as determined by baseline history physical

examination and vital sign examination blood pressure pulse rate respiration

rate and body temperature

3 Subjects with clinically acceptable findings as determined by haemogram

biochemistry urinalysis 12 lead ECG and chest X-ray if done

Exclusion Criteria

1 Known history of hypersensitivity to Diclofenac or related drugs

2 Requiring medication for any ailment having enzyme modifying activity in the previous 28 days prior to dosing day

3 Subjects who have taken prescription medications or over the counter products

including vitamins and minerals within 14 days prior to administration of IMP

Study & Design

Study Type
BA/BE
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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