Enhancing Preventive Therapy of Malaria In Children With Sickle Cell Anemia in East Africa (EPiTOMISE)

Malaria,Falciparum Clinical Trial

— EPiTOMISE  

Official title:

Enhancing Preventive Therapy of Malaria In Children With Sickle Cell Anemia in East Africa (EPiTOMISE)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03178643
• Other study ID #: Pro00077428
• Secondary ID: R01HL134211
• Status: Completed
• Phase: Phase 4
• Start date: January 23, 2018
• Est. completion date: December 16, 2020

Study information

• Verified date: April 2024
• Source: Duke University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a randomized, three-arm, open-label, clinical trial of malaria chemoprevention in children with sickle-cell anemia (SCA) at a single site in Homa Bay, Kenya. The study will enroll 246 children under 10 years of age, randomize participants 1:1:1 to one of three malaria chemoprevention regimens, and follow participants monthly for 12 months in order to record clinical episodes of malaria or SCA-related morbidity. Analyses will compare the efficacy of each regimen to prevent malaria and SCA morbidity.

Description:

Purpose of the study:

Primary Objective: To compare the efficacy of daily proguanil with monthly sulfadoxine/pyrimethanine-amodiaquine (SP-AQ) and with monthly dihydroartemisinin-piperaquine (DP) on the incidence of falciparum malaria in children with SCA.

Secondary Objective: To compare the efficacy of these malaria chemoprevention strategies on the incidence of major complications of SCA.

Background & significance

Over 240,000 children with sickle cell anemia (SCA) are born in Africa annually. This number will increase to over 350,000 annual births of children with SCA by the year 2050. Without sophisticated medical care, SCA patients in African settings die at young ages: in a Western Kenya cohort of newborns, 25% of SCA children died before their 3rd birthday. Caring effectively for these children will be a major challenge for developing medical and public health systems in Africa including Kenya, and modeling studies suggest that the adequate provision of effective preventive care can substantially reduce the mortality of these children. Preventive care for SCA children must be evidence-based and tailored to the unique epidemiology of comorbidities in African settings.

Children under 5 years of age in sub-Saharan Africa also suffer the majority of the annual 350 million infections and 500,000 deaths globally. Reducing this burden is a global public health priority, particularly in areas of high transmission like Western Kenya. In the absence of an effective vaccine, global malaria control requires effective treatments and a suite of preventive measures that act upon the parasite, environment, and host. Among these preventive strategies is the administration of prophylactic antimalarials to high risk groups, including pregnant women, infants, and children exposed to seasonal malaria transmission. In these high-risk groups malaria morbidity is substantially reduced by routine periodic intake of effective antimalarials.

Children with SCA are at high risk of life-threatening malaria. In East Africa children with SCA admitted to the hospital with malaria parasites were more likely to die than those without parasites. Malaria is also a precipitant of sickle-cell pain crises, by unclear mechanisms. It remains unclear how SCA influences the overall risk of malaria, because most studies have been hospital based and therefore unsuited to capture mild episodes. The twin observations that malaria is more severe in SCA children and precipitates painful crises in these children indicate that the prevention of P. falciparum infections is critical to prolong the survival of SCA children in malaria-endemic areas.

Design & procedures - This is a randomized, three-arm, open-label, clinical trial of malaria chemoprevention in children with sickle-cell anemia (SCA) at a single site in Homa Bay, Kenya. The study will enroll 246 children under 10 years of age, randomize participants 1:1:1 to one of three malaria chemoprevention regimens, and follow participants monthly for 12 months in order to record clinical episodes of malaria or SCA-related morbidity. Analyses will compare the efficacy of each regimen to prevent malaria and SCA morbidity.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 246
• Est. completion date: December 16, 2020
• Est. primary completion date: December 16, 2020
• Accepts healthy volunteers: No
• Gender: All
• Age group: 1 Year to 10 Years

Eligibility

Inclusion Criteria:

• Age greater than 12 months and less than 10 years at enrollment;

• Current attendance at or willingness to attend the study SCA clinic at HBCH;

• Residence in either Homa Bay County or the Rongo or Awendo sub-counties of Migori County;

• Confirmed hemoglobin genotype of HbSS by electrophoresis, HPLC, or PCR;

• No immediate, apparent, or reported plans to relocate residence from Homa Bay County or the Rongo or Awendo sub-counties of Migori County in the next 2 years;

• Ability to take oral medication and be willing to adhere to the medication regimen or caregiver willingness to give the medical regimen as prescribed;

• Ability and willingness of parent or legally authorized representative (LAR) to give informed consent;

• Assent of child in those > 7 years.

Exclusion Criteria:

• Taking routine antimalarial prophylaxis for another indication (including co-trimoxazole for HIV infection);

• Temperature of = 37.5C at screening or history of objective or subjective fever in the preceding 24 hours during screening;

• Known allergy or sensitivity to sulfadoxine, pyrimethamine, amodiaquine, proguanil, dihydroartemisinin, piperaquine, artemether, lumefantrine, pencillin (if under 5 years old), or derivatives of these compounds;

• Known chronic medical condition other than SCA (i.e. malignancy, HIV) requiring frequent medical attention;

• Currently participating in another clinical research study, or having participated in one in the prior 30 days;

• Living in the same household as a previously-enrolled study participant;

• Chronic use of medications known to prolong the QT interval in children (see Appendix J);

• Fridericia's corrected QT interval (QTcF) interval > 450msec.

Related Conditions & MeSH terms

• Anemia, Sickle Cell
• Malaria
• Malaria, Falciparum
• Malaria,Falciparum

Intervention

Drug:
• Proguanil Oral Tablet
Dosing of daily proguanil will be approximately 3mg/kg/day,
• Sulfadoxine/Pyrimethanine-Amodiaquine (SP-AQ)
Age 1-5 on Day 1: One tablet 500/25mg SP and one tablet 153mg AQ Day 2 and Day 3: one tablet 153 mg AQ only each day For ages 6-10: Day 1 - 1.5 tablets 500/25mg SP and 1.5 tablets 153mg AQ Days 2 and 3: 1.5 tablets 153mg AQ only each day
• Dihydroartemisinin-Piperaquine (DP)
3) The weight-based dosing of tablets of 40/320mg of DP is described below: Weight (kg) No. of 40/320mg tabs DP daily for 3 days = 5 ¼ 6-10 ½ 11-14 ¾ 15-19 1 20-23 1 ¼ 24-25 1 ½

Locations

Country	Name	City	State
Kenya	Homa Bay County Referral Hospital	Homa Bay Town	Homa Bay County

Sponsors (2)

Lead Sponsor	Collaborator
Duke University	National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

Kenya, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Incidence of Clinical Malaria Per Patient Year	The primary endpoint is the cumulative incidence of clinical malaria expressed as episodes per person-year at risk. Time at risk will begin when study participants are randomized and receive study drug (i.e. begin chemoprevention) and end when participants reach the end of the observation period.	12 months
Secondary	Number of Participants With Severe Anemia	E.g., hemoglobin <5.5 g/dL	12 months
Secondary	Number of Participants With Severe Malaria	Positive rapid diagnostic test (RDT).	12 months
Secondary	Number of Participants With Hospitalization for Malaria	Patient admitted to hospital for malaria with confirmed positive RDT.	12 months
Secondary	Number of Participants With Light Microscopy (LM)-Positive Malaria	LM-positive malaria defined as the reported presence of P. falciparum parasites detected by LM irrespective of RDT or other detection results.	12 months
Secondary	Number of Participants With Unconfirmed Malaria	Defined as the receipt of antimalarials for suspected malaria episodes that were not confirmed by any objective diagnostic test.	12 months
Secondary	Number of Participants With Fatal Malaria	Defined as death during hospitalization for malaria with positive RDT.	12 months
Secondary	Number of Participants With Asymptomatic Parasitization	Defined as the presence of parasites during routine follow-up visits as detected by PCR in patients without fever or a history of recent fever.	12 months
Secondary	Number of Participants With Painful Events	Pain lasting two hours or more without obvious cause.	12 months
Secondary	Number of Participants With Dactylitis	Pain or tenderness with or without swelling of the hands or feet.	12 months
Secondary	Number of Participants With Transfusions	Receipt of RBCs (red blood cells) from any caregiver for any indication.	12 months
Secondary	Number of Participants With Acute Chest Syndrome	Defined as a new pulmonary infiltrate and at least 3 of the following findings: chest pain, temperature elevation > 38.5°C, tachypnea, wheezing, or cough.	12 months
Secondary	Number of Participants With All-cause Hospitalization	Hospitalization at HBCH or any other inpatient facility with any admitting diagnosis.	12 months
Secondary	All-cause Deaths	Death by any cause.	12 months
Secondary	Molecular Markers of Malaria Parasite Drug Resistance	presence of SNPs in parasite genes that confer resistance to the study drugs	12 months