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Improving Neonatal Health Through Rapid Malaria Testing in Early Pregnancy With High-Sensitivity Diagnostics (INTREPiD)

Primary Purpose

Malaria,Falciparum, Malaria in Pregnancy, Malaria in Childbirth

Status
Not yet recruiting
Phase
Phase 4
Locations
International
Study Type
Interventional
Intervention
Malaria High-Sensitivity Rapid Diagnostic Test (HS-RDT)
Artemether-Lumefantrine 20 Mg-120 Mg Oral Tablet
Sponsored by
Duke University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional screening trial for Malaria,Falciparum

Eligibility Criteria

16 Years - 40 Years (Child, Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria: Aged between 16 years and 40 years (inclusive) Viable singleton pregnancy with gestational age estimated less than 13 6/7 weeks (inclusive) by ultrasound HIV-uninfected Willing to participate in the study schedule Planning to remain in the study area for the duration of pregnancy and 1 month after delivery Willing to deliver in a study-affiliated health facility Exclusion Criteria: High risk pregnancy that requires referral for specialized care by local guidelines Active medical problem at the time of screening requiring higher level care Antimalarial receipt in the 2 weeks prior to screening Past allergy to Artemether or Lumefantrine or another condition that prohibits the receipt of either drug Current participation in another clinical research study

Sites / Locations

  • Kinshasa School of Public Health
  • Moi University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

HS-RDT screening/AL treatment

Usual antenatal care

Arm Description

Pregnant women will be screened with a malaria HS-RDT and, if positive, treated with artemether-lumefantrine

Pregnant women will receive usual antenatal care

Outcomes

Primary Outcome Measures

Composite number of adverse pregnancy outcomes
Adverse pregnancy outcomes defined as low birth weight (<2500 grams) OR preterm (< 37 0/7 weeks) OR small for gestational age (GA) (< 10th percentile weight for GA) OR pregnancy loss, defined as a. spontaneous abortion ( loss < 22 0/7 weeks gestation) OR b. stillbirth (loss ≥ 22 0/7 weeks gestation) OR neonatal death (livebirth with death prior to the 28th day of life).

Secondary Outcome Measures

Birthweight
Birthweight in grams
Number of infants with low birthweight
< 2500 grams, livebirth
Gestational age (GA)
GA at delivery in weeks/days, livebirth
Preterm
< 37 0/7 weeks, livebirth
Number of infants that are small for gestational age
Weight for gestational age < 10th percentile, livebirth
Number of adverse newborn outcomes
low birthweight OR preterm OR small for gestational age
Number of spontaneous abortions
Pregnancy loss < 22 0/7 weeks gestation
Number of stillbirths
Pregnancy loss ≥ 22 0/7 weeks gestation
Number of early fetal deaths
Pregnancy loss 22 0/7 - 27 6/7 weeks gestation
Number of late fetal deaths
Pregnancy loss ≥ 28 0/7 weeks gestation
Number of pregnancy losses
Spontaneous abortion OR stillbirth
Number of neonatal deaths
Before the 28th day of life, livebirth
Number of perinatal deaths
Late fetal death OR Neonatal death
Incidence of clinical malaria during pregnancy
Maternal symptoms with peripheral malaria parasitemia detected by light microscopy or rapid diagnostic test
Number of mothers with peripheral parasitemia at delivery
Maternal peripheral parasitemia at delivery by PCR
Mean maternal hemoglobin concentration
Maternal hemoglobin (g/dL)
Number of mothers with anemia at delivery
Maternal Hb concentration ≤ 11 g/dL
Number of mothers with severe anemia at delivery
Maternal Hb concentration ≤ 7 g/dL

Full Information

First Posted
February 24, 2023
Last Updated
August 16, 2023
Sponsor
Duke University
Collaborators
National Institute of Allergy and Infectious Diseases (NIAID)
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1. Study Identification

Unique Protocol Identification Number
NCT05757167
Brief Title
Improving Neonatal Health Through Rapid Malaria Testing in Early Pregnancy With High-Sensitivity Diagnostics
Acronym
INTREPiD
Official Title
Improving Neonatal Health Through Rapid Malaria Testing in Early Pregnancy With High-Sensitivity
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Not yet recruiting
Study Start Date
September 2023 (Anticipated)
Primary Completion Date
February 2025 (Anticipated)
Study Completion Date
February 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Duke University
Collaborators
National Institute of Allergy and Infectious Diseases (NIAID)

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of the INTREPiD study is to compare 1st trimester screening for malaria parasites with a high-sensitivity malaria rapid diagnostic test followed by treatment of test-positive women with artemether-lumefantrine (AL) against usual antenatal care on a composite adverse pregnancy outcome including low birth weight, small for gestational age, preterm, fetal loss, or neonatal death.
Detailed Description
INTREPiD is a two-arm, open-label, parallel-assignment randomized trial of a strategy of 1st trimester screening for P. falciparum parasites with a high-sensitivity rapid diagnostic test (HS-RDT). Participants will be women of all gravidities presenting to antenatal clinics in the 1st trimester in sites endemic for P. falciparum malaria in Kenya and the Democratic Republic of the Congo. Following consent and enrollment, women will be allocated 1:1 to either usual antenatal care or to the intervention. The intervention will be a single screening in the 1st trimester for P. falciparum infection in maternal peripheral blood with a HS-RDT. Women who test positive for P. falciparum on HS-RDT testing will be treated with a single course of Artemether-Lumefantrine (AL) and then returned to usual antenatal care. Participants will be followed through delivery and then through their offspring's first month of life. The Hypothesis is that, compared to usual antenatal care, screening women in the 1st trimester for P. falciparum and treating them if positive with AL will reduce the risk of an adverse pregnancy outcome.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malaria,Falciparum, Malaria in Pregnancy, Malaria in Childbirth, Pregnancy, Neonatal Health, Low Birthweight, Stillbirth, Gestational Age and Weight Conditions, Preterm Birth

7. Study Design

Primary Purpose
Screening
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Random assignment to either a) usual antenatal care or b) testing for malaria with a high-sensitivity rapid diagnostic test followed by treatment with artemether-lumefantrine if tested positive
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
2500 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
HS-RDT screening/AL treatment
Arm Type
Experimental
Arm Description
Pregnant women will be screened with a malaria HS-RDT and, if positive, treated with artemether-lumefantrine
Arm Title
Usual antenatal care
Arm Type
No Intervention
Arm Description
Pregnant women will receive usual antenatal care
Intervention Type
Diagnostic Test
Intervention Name(s)
Malaria High-Sensitivity Rapid Diagnostic Test (HS-RDT)
Other Intervention Name(s)
NxTek™ Eliminate Malaria P.f, 05FK140 (Global), 05FK141 (Global), 05FK142 (Global), 05FK143 (Global), Alere Malaria Ag P.f
Intervention Description
Detection of Plasmodium falciparum HRP-II antigen1 Method: Lateral Flow; Time to Result: 20 minutes; Sample Type: Fingerstick Whole Blood; Sample Volume: 5µl; Storage Conditions: 1-30°C; Shelf Life: 12 months; Sensitivity/Specificity: 99.0%/98.6%
Intervention Type
Drug
Intervention Name(s)
Artemether-Lumefantrine 20 Mg-120 Mg Oral Tablet
Other Intervention Name(s)
AL, Coartem
Intervention Description
oral tablets: 6 doses of 80/480 mg over 3 days
Primary Outcome Measure Information:
Title
Composite number of adverse pregnancy outcomes
Description
Adverse pregnancy outcomes defined as low birth weight (<2500 grams) OR preterm (< 37 0/7 weeks) OR small for gestational age (GA) (< 10th percentile weight for GA) OR pregnancy loss, defined as a. spontaneous abortion ( loss < 22 0/7 weeks gestation) OR b. stillbirth (loss ≥ 22 0/7 weeks gestation) OR neonatal death (livebirth with death prior to the 28th day of life).
Time Frame
Enrollment to 28 days Post-delivery (including each antenatal care visit)
Secondary Outcome Measure Information:
Title
Birthweight
Description
Birthweight in grams
Time Frame
Delivery
Title
Number of infants with low birthweight
Description
< 2500 grams, livebirth
Time Frame
Delivery
Title
Gestational age (GA)
Description
GA at delivery in weeks/days, livebirth
Time Frame
Delivery
Title
Preterm
Description
< 37 0/7 weeks, livebirth
Time Frame
Delivery
Title
Number of infants that are small for gestational age
Description
Weight for gestational age < 10th percentile, livebirth
Time Frame
Delivery
Title
Number of adverse newborn outcomes
Description
low birthweight OR preterm OR small for gestational age
Time Frame
Delivery
Title
Number of spontaneous abortions
Description
Pregnancy loss < 22 0/7 weeks gestation
Time Frame
Delivery
Title
Number of stillbirths
Description
Pregnancy loss ≥ 22 0/7 weeks gestation
Time Frame
Delivery
Title
Number of early fetal deaths
Description
Pregnancy loss 22 0/7 - 27 6/7 weeks gestation
Time Frame
Delivery
Title
Number of late fetal deaths
Description
Pregnancy loss ≥ 28 0/7 weeks gestation
Time Frame
Delivery
Title
Number of pregnancy losses
Description
Spontaneous abortion OR stillbirth
Time Frame
Delivery
Title
Number of neonatal deaths
Description
Before the 28th day of life, livebirth
Time Frame
Delivery to 28 days Post-delivery
Title
Number of perinatal deaths
Description
Late fetal death OR Neonatal death
Time Frame
Delivery to 28 days Post-delivery
Title
Incidence of clinical malaria during pregnancy
Description
Maternal symptoms with peripheral malaria parasitemia detected by light microscopy or rapid diagnostic test
Time Frame
Enrollment to Delivery (including each antenatal care visit)
Title
Number of mothers with peripheral parasitemia at delivery
Description
Maternal peripheral parasitemia at delivery by PCR
Time Frame
Delivery
Title
Mean maternal hemoglobin concentration
Description
Maternal hemoglobin (g/dL)
Time Frame
Enrollment and Delivery
Title
Number of mothers with anemia at delivery
Description
Maternal Hb concentration ≤ 11 g/dL
Time Frame
Delivery
Title
Number of mothers with severe anemia at delivery
Description
Maternal Hb concentration ≤ 7 g/dL
Time Frame
Delivery
Other Pre-specified Outcome Measures:
Title
Number of maternal serious adverse events
Description
Serious adverse events in the mothers
Time Frame
Enrollment to 28 days Post-delivery
Title
Number of infants with congenital malformations
Description
Congenital malformations identified within the first 28 days of birth
Time Frame
Delivery to 28 days Post-delivery
Title
Number of offspring with the need for hospitalization or acute medical evaluation
Description
Hospitalization or acute medical evaluation within the first 28 days of life
Time Frame
Delivery to 28 days Post-delivery

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
16 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Aged between 16 years and 40 years (inclusive) Viable singleton pregnancy with gestational age estimated less than 13 6/7 weeks (inclusive) by ultrasound HIV-uninfected Willing to participate in the study schedule Planning to remain in the study area for the duration of pregnancy and 1 month after delivery Willing to deliver in a study-affiliated health facility Exclusion Criteria: High risk pregnancy that requires referral for specialized care by local guidelines Active medical problem at the time of screening requiring higher level care Antimalarial receipt in the 2 weeks prior to screening Past allergy to Artemether or Lumefantrine or another condition that prohibits the receipt of either drug Current participation in another clinical research study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Stephen James, MPH
Phone
919-668-0420
Email
stephen.james@duke.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Irene Okumu
Phone
919-660-6321
Email
irene.okumu@duke.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Steve M Taylor, MD, MPH
Organizational Affiliation
Duke University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kinshasa School of Public Health
City
Kinshasa
Country
Congo, The Democratic Republic of the
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Antoinette Tshefu, MD, PhD, MPH
Phone
+243998551185
Email
antotshe@yahoo.com
First Name & Middle Initial & Last Name & Degree
Jean Okitawutshu, MD
Email
jeanokitawutshu@gmail.com
First Name & Middle Initial & Last Name & Degree
Antoinette Tshefu, MD, PhD, MPH
Facility Name
Moi University
City
Eldoret
Country
Kenya
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jeremiah Laktabai, MBChB, MMED
Phone
+254532033235
Email
jklaktabai@gmail.com
First Name & Middle Initial & Last Name & Degree
Joseph Kipkoech
Phone
+254720393547
Email
josepheddykipkoech@gmail.com
First Name & Middle Initial & Last Name & Degree
Jeremiah Laktabai, MBChB, MMED

12. IPD Sharing Statement

Plan to Share IPD
No
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Description
Organization WH. Every Newborn: an action plan to end preventable deaths.
URL
http://apps.who.int/iris/handle/10665/338496
Description
WHO. Recommendations on intermittent screening and treatment in pregnancy and the safety of ACTs in the first trimester.

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Improving Neonatal Health Through Rapid Malaria Testing in Early Pregnancy With High-Sensitivity Diagnostics

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