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Malaria, Vivax clinical trials

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NCT ID: NCT04368910 Terminated - Malaria Clinical Trials

Safety and Efficacy of Pyronaridine Artesunate Vs Chloroquine in Children and Adult Patients With Acute Vivax Malaria

Start date: September 6, 2007
Phase: Phase 3
Study type: Interventional

The primary objective of this clinical study is to compare the efficacy and safety of the fixed combination of pyronaridine artesunate (180:60 mg) with that of standard chloroquine therapy in children and adults with acute, uncomplicated Plasmodium vivax (P. vivax) malaria

NCT ID: NCT03337152 Terminated - Malaria, Vivax Clinical Trials

Assessing a Risk Model for G6PD Deficiency

Start date: May 7, 2018
Phase: Phase 4
Study type: Interventional

A clinical study designed to develop and inform an individual risk of hemolysis model based on individual red blood cell G6PD levels. Volunteers who are eligible to treatment with primaquine as per national guidelines and with confirmed normal G6PD levels as per the fluorescent spot test will be exposed to treatment regimens of either primaquine alone for 14 days or 3 day chloroquine with concomitant primaquine for 14 days. The volunteers will be followed intensively during treatment and for 14 days after treatment for haematologic measures, G6PD quantification, and drug level assays.

NCT ID: NCT02110784 Terminated - Malaria, Vivax Clinical Trials

Eurartesim® in Patients With Imported Uncomplicated Plasmodium Vivax Malaria

Start date: June 18, 2014
Phase: Phase 2
Study type: Interventional

The aim of the present study is to investigate the efficacy, safety and tolerability of a therapeutic course of Eurartesim® in travellers who contracted malaria due to infection by P. vivax in endemic countries.

NCT ID: NCT01107145 Terminated - Clinical trials for Plasmodium Vivax Malaria

Efficacy of Artemisinin Combination Therapies for the Treatment of Uncomplicated P. Vivax in Pregnancy in Brazil (PAACT-PV)

PAACT-PV
Start date: February 2011
Phase: Phase 4
Study type: Interventional

The current treatment recommendations for P. vivax in pregnant and non-pregnant individuals are to use chloroquine; in non-pregnant patients this is followed by primaquine to prevent relapse. As primaquine can not be used in pregnant women, these women remain at risk of relapse. As there is increasing concern about chloroquine resistant P. vivax in this region, there is a need to identify alternative treatment options. The artemisinin combination therapies are recommended for use against P. falciparum infections in pregnant women after the 1st trimester; additional data are needed to support the use of these drugs against P. vivax.

NCT ID: NCT00138489 Terminated - Clinical trials for Plasmodium Vivax Malaria

Papua New Guinean Duffy Negativity And Vivax Malar

Start date: February 10, 2004
Phase:
Study type: Observational

The purpose of this study is to learn more about vivax malaria in very young children, how the growth of children is affected by malaria infections, and how inherited traits protect children from getting malaria. Participants will be 266 children 24 months of age or younger who live in certain villages in East Sepik Province, Papua New Guinea, where malaria is very common. The study also will find out how malaria spreads in the area. By learning how and when a child develops resistance to vivax malaria, researchers can try to find ways to help people from getting it. And, they can get a better understanding of how inherited traits influence all types of malaria infections. In this study, the parent and child will be visited by the study team or health workers every week to check health and bednet use. Every 2 weeks, the study team will take a small blood sample to check for malaria and take measurements to study the child's growth. Participants will be followed for up to 2 years.