Prevention of P. Vivax Malaria During Pregnancy in Bolivia

The recruitment status of this study is unknown because the information has not been verified recently.
Verified February 2006 by Institut de Recherche pour le Developpement.
Recruitment status was  Not yet recruiting
Sponsor:
Collaborators:
Instituto Nacional de Laboratorios de Salud (INLASA)
Pan American Health Organization
Ministry of Health, Bolivia
Information provided by:
Institut de Recherche pour le Developpement
ClinicalTrials.gov Identifier:
NCT00290420
First received: February 9, 2006
Last updated: NA
Last verified: February 2006
History: No changes posted

February 9, 2006
February 9, 2006
March 2006
Not Provided
Incidence of women presenting a malaria attack during pregnancy
Same as current
No Changes Posted
  • proportions of mothers with placental plasmodial infection
  • proportions of mothers with moderate to severe anaemia (<8g/dl) at delivery
  • maternal haemoglobin rate at delivery
  • proportions of women with parasitaemia during pregnancy and at delivery
  • mean parasites densities of women with parasitaemia during pregnancy and at delivery
  • proportions of children with low birthweight (<2,500 grams)
  • mean birthweight
  • proportions of preterm deliveries
Same as current
Not Provided
Not Provided
 
Prevention of P. Vivax Malaria During Pregnancy in Bolivia
Prevention of P. Vivax Malaria During Pregnancy: Effects on Mother and Child Health in Santa Cruz, Bolivia. Open, Multicentric, Randomized Clinical Trial, Comparing Prophylaxis Once a Week to Malaria Attack Treatment, Both by Chloroquine.

The purpose of this study is to determine which, between weekly prophylaxis or malaria attack treatment, both by chloroquine, is the most appropriate way to protect women and foetus from P. vivax malaria infection during pregnancy.

It has been demonstrated that malaria is responsible for anaemia during pregnancy and reduces birth weight among newborns. In Bolivia, malaria is mostly caused by P. vivax. Maternal and foetal consequences of P. vivax infections have been poorly investigated until now, over all in South America. In fact, recommendations for the protection of pregnant women from malaria in Bolivia have not been clearly established. Prophylaxis by chloroquine is still recommended in other continents than Africa, mainly because chloroquine resistances are still uncommon in P. vivax species. The alternative way to protect women during pregnancy is to treat malaria attacks during antenatal visits. For this purpose, we will realize a study in order to assess the most appropriate way to protect women and foetus from malaria infection, i.e. weekly prophylaxis or mild malaria attack treatment, both by chloroquine. By realizing a randomized and multicentric clinical trial on 800 women in each group, we will compare the impact on maternal malaria attack incidence rates, on proportions of mothers with anaemia, on low-birth weight and on positive parasitaemias during pregnancy and at delivery, of weekly prophylaxis and mild malaria attack diagnosis and treatment. The study will be undertaken during 18 months in the region of Santa Cruz and will give important information to the Bolivian Ministry of Health for establishing national recommendations.

Interventional
Phase 4
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Prevention
Malaria
Drug: Chloroquine prophylaxis
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Not yet recruiting
1600
November 2007
Not Provided

Inclusion Criteria:

  • Pregnancy between 4 to 36 weeks of gestation
  • Intention to deliver at the maternity clinics
  • Residence near the maternity clinics
  • Written informed consent (parents or tutors if aged<18 years)

Exclusion Criteria:

  • Pregnancy prior to 4 weeks or after 36 weeks of gestation
  • Allergy to chloroquine
  • Clinical signs of hepatic or renal alteration
  • Inability to take drugs by oral route
  • Presence of effective uterine contractions
Female
Not Provided
Yes
Contact: Agnès Le Port, MSc (00 591 2) 222 19 01 aleport@free.fr
Bolivia
 
NCT00290420
IRD/Prevmal/Bol/06
Not Provided
Not Provided
Institut de Recherche pour le Developpement
  • Instituto Nacional de Laboratorios de Salud (INLASA)
  • Pan American Health Organization
  • Ministry of Health, Bolivia
Study Director: Michel Cot, MD-PhD Institut de Recherche pour le Developpement
Study Director: Laurent Brutus, MD-MSc Institut de Recherche pour le Développement, IRD, Bolivia
Principal Investigator: Agnès Le Port, MSc Institut de Recherche pour le Développement, IRD, Bolivia
Institut de Recherche pour le Developpement
February 2006

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP