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Tracking Artemisinin Resistance in India.

Not Applicable
Conditions
Health Condition 1: null- Uncomplicated Plasmodium falciparum malaria
Registration Number
CTRI/2015/10/006243
Lead Sponsor
ational Institute of Malaria ResearchICMR
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
140
Inclusion Criteria

Acute uncomplicated P. falciparum malaria, confirmed by positive blood smear with asexual forms of P. falciparum

Asexual P. falciparum parasitaemia: 10,000 to 100,000/uL, determined on a thin or thick blood film

Fever defined as > 37.5°C temperature or a history of fever within the last 24 hours

Written informed consent (by legally acceptable representative in case of children)

Willingness and ability of the patients/guardians to comply with the study protocol for the duration of the study

Exclusion Criteria

Signs of severe/complicated malaria

Haematocrit < 25% or haemoglobin (Hb) < 8 g/dL at enrollment

Acute illness other than malaria requiring treatment

For females: pregnancy, lactating

Patients who have received artemisinin or a derivative or an artemisinin-containing combination therapy (ACT) within the previous 7 days

History of allergy or known contraindication to artemisinins, or to the ACT to be used at the site

Previous splenectomy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Within one year the study is expected to produce data of the prevalence and severity of artemisinin resistance if any.Fro this Parasite clearrance time PCT will be calculated.Timepoint: 28 days followup
Secondary Outcome Measures
NameTimeMethod
Parasite reduction rates and ratios at 24 and 48 hours by microscopy and quantitative PCR <br/ ><br>Time for parasite count to fall to 50%, 90% and 99% of initial parasite density <br/ ><br>Fever clearance time <br/ ><br>Proportion of patients with gametocytemia before, during and after treatment with artesunate, assessed at admission, on days 3, 7 and 14 <br/ ><br>Parasite molecular markers of drug resistanceTimepoint: 28 days follow up
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