CTRI/2017/08/009579
Recruiting
Phase 2
A prospective study to evaluate the safety and efficacy of Carica papaya leaf extract (Oral Caripill) in the treatment of severe thrombocytopenia (s30,000/µl) in dengue - AIMSCARI
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Micro Labs Limited
- Enrollment
- 84
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Provide signed and dated informed consent form
- •2\.Willing to comply with all study procedures and be available for the duration of the study
- •3\.Male or female, aged greater than or equal to 18 yrs of age. Clinically diagnosed of dengue and a peripheral platelet count of less than or equal to 30,000/µL.
- •4\.A laboratory positive diagnosis of dengue confirmed by a positive NS1 ELISA test and/or detection of viral RNA by real time PCR assay.
Exclusion Criteria
- •1\.Pregnancy and lactation.
- •2\.Patients who has been given steroids for thrombocytopenia and also those who have been transfused platelets before starting the drug
- •3\.Taking indigenous medicines.
- •4\.Creatine kinase (CK) \>1000 U/L
Outcomes
Primary Outcomes
Not specified
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