Efficacy of Intermittent Screening and Treatment or Intermittent Preventive Treatment (IPT) With Dihydroartemisinin-Piperaquine, Versus IPT With Sulfadoxine-Pyrimethamine for the Control of Malaria in Pregnancy in Kenya

Pregnancy Clinical Trial

— STOP MiP KENYA  

Official title:

Intermittent Screening and Treatment (IST) or Intermittent Preventive Treatment (IPT) With Dihydroartemisinin-Piperaquine, Versus IPT With Sulfadoxine-Pyrimethamine for the Control of Malaria in Pregnancy in Kenya: a Randomized Controlled Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01669941
• Other study ID #: STOPMiP-KENYA
• Status: Completed
• Phase: Phase 4
• First received: August 15, 2012
• Last updated: March 3, 2017
• Start date: August 2012
• Est. completion date: December 2015

Study information

• Verified date: March 2017
• Source: Kenya Medical Research Institute
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Malaria in pregnancy (MiP) due to Plasmodium falciparum infection is a major cause of maternal morbidity and poor birth outcomes. Intermittent preventive treatment in pregnancy (IPTp) with Sulfadoxine pyrimethamine (SP), the administration of SP at predefined intervals in the second and third trimesters of pregnancy irrespective of the presence of malaria parasitemia, is currently recommended for HIV-negative women in all areas with stable moderate to high transmission of malaria. Due to increasing resistance to SP, it is no longer used as a treatment for symptomatic malaria, and the efficacy of IPTp-SP seems to be decreased. This study aims to look at a new drug, Dihydroartemisinin-Piperaquine (DP) for IPTp, as well as to explore the strategy of intermittent screening and treatment in pregnancy (ISTp) with DP. This strategy uses increased screening at time of focused antenatal care (FANC) with treatment of women who screen positive.

The hypothesis is that the efficacy of both IPTp-DP and ISTp-DP will be associated with a reduction in malaria infection at delivery among HIV(-) women when compared to IPTp-SP, in an area with decreasing malaria transmission and high levels of SP resistance in Kenya.

Description:

Malaria in pregnancy (MiP) due to Plasmodium falciparum infection is a major cause of maternal morbidity and poor birth outcomes. Pregnant women are at increased risk of more frequent and severe malaria infections than are non-pregnant women. Intermittent preventive treatment in pregnancy (IPTp), the administration of treatment doses of an antimalarial at predefined intervals in the second and third trimesters of pregnancy irrespective of the presence of malaria parasitemia, is currently recommended for HIV-negative women in all areas with stable moderate to high transmission of malaria. The strategy is thought to work by providing intermittent clearance or suppression of parasites in the placenta, and preventing new infections from occurring through the prophylactic effect of the recommended drug for IPTp, sulfadoxine-pyrimethamine (SP).

SP is the only drug currently used for IPTp. Due to increasing resistance to SP, it is no longer used as a treatment for symptomatic malaria, however, IPTp with SP remains effective even in areas where SP resistance in children under five (determined by in vivo efficacy studies) is up to 26%. SP therefore continues to be used for IPTp in many countries where it is no longer used for treatment of symptomatic malaria. However, more recent data from northern Tanzania and Malawi indicate that at higher rates of resistance, IPTp-SP may no longer be effective, and could potentially be harmful.

In view of this data, a search for alternatives to IPTp-SP is warranted. One strategy would be to choose a different drug for IPTp. Of the available combinations, Dihydroartemisinin-Piperaquine (DP) remains one of the most attractive options because of the long half-life of piperaquine (PQ) and the demonstrated efficacy and safety in pregnancy. Another strategy to consider is intermittent screening and treatment in pregnancy (ISTp), whereby there is increased screening at time of focused antenatal care (FANC) with treatment of women who screen positive. The same properties (long half-life, tolerability, safety, once daily dosing) which make DP a good choice for IPTp also make it one of the best available options for ISTp.

This study aims to compare the efficacy of IPTp-SP against that of IPTp-DP and ISTp-DP to determine if these alternate strategies are associated with a reduction in malaria infection at delivery among HIV(-) women in an area with decreasing malaria transmission and high levels of SP resistance in Kenya.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 1546
• Est. completion date: December 2015
• Est. primary completion date: October 2014
• Accepts healthy volunteers: No
• Gender: Female
• Age group: N/A and older

Eligibility

Inclusion Criteria:

1. Viable pregnancy assessed by Doppler

2. Gestational age 16 to 32 weeks (inclusive) by fundal height

3. No history of IPTp use during this pregnancy

4. Willing to participate and complete the study schedule

5. Willing to sign or thumb print informed consent

6. Resident of study area and intending to stay in the area for the duration of the follow-up

7. Willing to deliver in the labor ward of the study clinic or hospital

8. HIV negative at enrolment

Exclusion Criteria:

1. HIV positive or unknown

2. Residence outside study area or planning to move out in the 12 months following enrolment

3. High risk pregnancy, including any pre-existing illness likely to cause complication of pregnancy (hypertension, diabetes, asthma, epilepsy, renal disease, liver disease, fistula repair, leg or spine deformity)

4. Severe anemia requiring blood transfusion (Hb = 7.0 g/dL) at enrolment

5. Known allergy or previous adverse reaction to any of the study drugs

6. Unable to give informed consent (for example due to mental disability)

7. Previous inclusion in the same study

8. Gestational age >32 weeks

9. Previous IPTp during the current pregnancy

10. Participating in other malaria intervention studies

11. Known or suspected cardiac disease

12. Patients taking drugs in any of the following classes: antiarrhythmic agents, neuroleptics, macrolides, and certain antimalarial drugs such as mefloquine, chloroquine, halofantrine and lumefantrine.

Related Conditions & MeSH terms

• Malaria
• Pregnancy

Intervention

Drug:
• IPTp-SP
3 tablets of sulfadoxine (500 mg) and pyrimethamine (25 mg) given at each ANC visit
• IPTp-DP
At each ANC visit: treatment with Dihydroartemisinin-piperaquine for three days, with the daily number of tablets depending on the weight of the woman; two tablets for women weighing 24- 35.9kg, three tablets for women weighing 36 to 74.9 kg, and four tablets for women weighing 75kg or more. The first dose will be observed; the woman will be given the additional 2 doses to take at home and there may be a home visit to confirm that the tablets were taken.
• ISTp-DP
At each ANC visit, women will be screened for malaria using a combined HRP-2/ pLDH (P. falciparum/ pan-malaria) rapid diagnostic test, and if positive, treated with dihydroartemisinin-piperaquine. Each tablet will contain 40 mg dihydroartemisinin and 320 mg piperaquine. Treatment will be given for three days, with the daily number of tablets depending on the weight of the woman; two tablets for women weighing 24- 35.9kg, three tablets for women weighing 36 to 74.9 kg, and four tablets for women weighing 75kg or more. The first dose will be observed; the woman will be given the additional 2 doses to take at home

Locations

Country	Name	City	State
Kenya	Bondo District Hospital	Bondo
Kenya	Madiany sub-District Hospital	Madiany
Kenya	Lwak Mission Hospital	Rarieda	Nyanza
Kenya	Siaya District Hospital	Siaya	Nyanza

Sponsors (4)

Lead Sponsor	Collaborator
Kenya Medical Research Institute	Centers for Disease Control and Prevention, Liverpool School of Tropical Medicine, London School of Hygiene and Tropical Medicine

Country where clinical trial is conducted

Kenya, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maternal malaria at delivery	Active or recent infection at delivery measured as the composite of peripheral and placental malaria, detected by: positive peripheral blood smear or RDT or positive placental smear, RDT, or histopathology	Delivery
Secondary	Decreased fetal morbidity	Decreased fetal morbidity, defined as the composite of any of the following: Preterm birth (birth before 37 weeks gestation); Low-birth-weight (birth weight under 2,500 grams); Small for gestational age (SGA) defined as a binary outcome of <10th percentile of fetal weight for attained gestational age using the Landis fetal weight nomogram from the Democratic Republic of Congo	Delivery
Secondary	Frequency of fetal congenital malformations		At delivery
Secondary	Pharmacokinetics- piperaquine level		At baseline, and day 2 and day 7 following dosing.
Secondary	level of antibodies to variant surface antigens (VSAs)		At delivery
Secondary	Frequency of maternal adverse events		At each ANC visit and at delivery

External Links

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