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A clinical trial to study the effects of Caripill drug on severely low platelet counts in patients with dengue disease

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

Status
Recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/08/009579
Enrollment
100
Registered
2017-08-31
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: null- Dengue

Interventions

Intervention1: Caripill: Carica Papaya Leaf Extract tablets 1100mg t.i.d for 5 days Control Intervention1: Placebo: 1100mg t.i.d for 5 days

Sponsors

Micro Labs Limited
Lead Sponsor

Eligibility

Inclusion 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

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

Design outcomes

Primary

MeasureTime frame
Comparison of peak platelet counts and hematocrit levels between the treatment and placebo groups. Comparison of the frequency and type of blood product, more specifically platelet transfusions between the treatment and placebo groups. Timepoint: 12 months

Secondary

MeasureTime frame
Correlation of platelet counts with phases of dengue Compare and evaluate the correlation of viremia with peripheral platelet counts between the treatment and placebo groupsTimepoint: 12 months

Countries

India

Contacts

Public ContactDr Vidya P Menon

Amrita Institute of Medical Sciences

veenam20656@aims.amrita.edu8289874024

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026