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Nutritional and Anti-infective Interventions for Malnutrition in Pregnancy (Beleuman Welbodi)

Primary Purpose

Pregnancy, Malnutrition in Pregnancy, Nutrition Disorders

Status
Completed
Phase
Not Applicable
Locations
Sierra Leone
Study Type
Interventional
Intervention
Ready-to-use-supplementary food
Corn-soy-blend
Monthly intermittent preventive treatment of malaria during pregnancy (IPTp)
Standard intermittent preventive treatment of malaria during pregnancy (IPTp)
Insecticide-treated mosquito net
Azithromycin
Albendazole
Bacterial vaginosis testing and treatment
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pregnancy

Eligibility Criteria

14 Years - undefined (Child, Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Pregnant women and consenting to study participation
  • Fundal height not greater than 32 cm
  • Mid-upper arm circumference ≤23 cm
  • Planning to reside in the study area during pregnancy and 6 months post partum
  • Attending 1 of the 40 antenatal clinic sites

Exclusion Criteria:

  • < 16 years of age without adult willing to consent
  • Known pregnancy complications such as gestational diabetes, pre-eclampsia, hypertension

Sites / Locations

  • 1 Moriba Street

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Ready-to-use supplementary food + anti-infective bundle

Corn-soy-blend

Arm Description

The women randomized to this arm will receive a ready-to-use-supplementary food (RUSF) designed specifically for pregnancy. The RUSF will provide a total of 520 kcal, 18 g protein, and 200% of recommended daily allowance (RDA) for most micronutrients during pregnancy. The supplement is also optimized to provide excellent protein quality and optimal polyunsaturated fatty acid composition. These women will receive 5 anti-infective interventions: 1) insecticide-treated mosquito net, 2) monthly intermittent preventive treatment of malaria during pregnancy (IPTp) 3) azithromycin at the second and third trimester 4) albendazole given in second trimester, and 5) bacterial vaginosis testing and treatment at enrollment and again at weeks 28-34

The women randomized to this arm will receive the standard of care for Sierra Leone. The treatment provided to women in this group includes 3.5 kg super cereal with 350 g vegetable oil every two weeks. This provides 250 mg portion/day of the super cereal and 25g oil/day for the mother. Women will receive the food for the duration of their pregnancy. These women will receive the current recommendations of the government of Sierra Leone, which includes standard intermittent preventive treatment of malaria during pregnancy (IPTp) of 2 doses of sulfadoxine/ pyrimethamine, iron and folic acid supplement with a goal of 90 pills/pregnancy, an insecticide-treated mosquito net, and albendazole for deworming in the second trimester.

Outcomes

Primary Outcome Measures

Infant birth length
mean birth length of infants born to mothers in the study

Secondary Outcome Measures

Maternal weight gain
Average weekly weight gain of women in the study
Proportion recovered from maternal malnutrition
proportion of women who reach mid-upper-arm circumference (MUAC) > 23 cm
Premature delivery
proportion of infants born prematurely
Newborn head circumference
mean head circumference of infants born to women in the study
Infant birth weight
mean birth weights of infants born to mothers in the study
Infant weight at 6 weeks, 3 and 6 months
infant ponderal growth
Infant length at 6 weeks, 3 and 6 months
infant linear growth
Infant survival at 3 and 6 months
survival of infants in the study

Full Information

First Posted
March 5, 2017
Last Updated
January 5, 2021
Sponsor
Washington University School of Medicine
Collaborators
The Children's Investment Fund Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT03079388
Brief Title
Nutritional and Anti-infective Interventions for Malnutrition in Pregnancy (Beleuman Welbodi)
Official Title
Randomized Control Trial of the Use of Supplementary Food and Measures to Control Inflammation in Malnourished Pregnant Women to Improve Birth Outcomes
Study Type
Interventional

2. Study Status

Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
February 27, 2017 (Actual)
Primary Completion Date
September 24, 2019 (Actual)
Study Completion Date
February 24, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Washington University School of Medicine
Collaborators
The Children's Investment Fund Foundation

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Acute malnutrition in pregnancy is a risk factor for adverse outcomes in mothers and their unborn children. Undernutrition during pregnancy can result in maternal complications such as life-threatening hemorrhage and hypertensive disorders of pregnancy and infant complications such as intrauterine growth retardation, low birth weight, pre-term delivery and poor cognitive development. Poor women in the developing world are at heightened risk of malnutrition due to inadequate dietary intake and are subject to transmission of a number of infections including malaria, intestinal helminths, and genitourinary infections. Food interventions for malnutrition may be less effective under conditions with excessive inflammation and infection, and especially so during pregnancy. Without specifically addressing treatment for infections, undernourished mothers may be less responsive to nutritional interventions. The benefits of treating both malnutrition and common infections simultaneously remain largely unstudied. This study tests the hypothesis that malnourished pregnant women receiving 100 grams per day of a specially formulated ready-to-use supplementary food in addition to a combination of 5 anti-infective interventions will have greater weight gain in pregnancy and deliver larger, longer infants than women receiving the standard of care. The outcome of the pregnancy and maternal nutritional status will be followed until 6 months after delivery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pregnancy, Malnutrition in Pregnancy, Nutrition Disorders, Stunting

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
1489 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ready-to-use supplementary food + anti-infective bundle
Arm Type
Experimental
Arm Description
The women randomized to this arm will receive a ready-to-use-supplementary food (RUSF) designed specifically for pregnancy. The RUSF will provide a total of 520 kcal, 18 g protein, and 200% of recommended daily allowance (RDA) for most micronutrients during pregnancy. The supplement is also optimized to provide excellent protein quality and optimal polyunsaturated fatty acid composition. These women will receive 5 anti-infective interventions: 1) insecticide-treated mosquito net, 2) monthly intermittent preventive treatment of malaria during pregnancy (IPTp) 3) azithromycin at the second and third trimester 4) albendazole given in second trimester, and 5) bacterial vaginosis testing and treatment at enrollment and again at weeks 28-34
Arm Title
Corn-soy-blend
Arm Type
Active Comparator
Arm Description
The women randomized to this arm will receive the standard of care for Sierra Leone. The treatment provided to women in this group includes 3.5 kg super cereal with 350 g vegetable oil every two weeks. This provides 250 mg portion/day of the super cereal and 25g oil/day for the mother. Women will receive the food for the duration of their pregnancy. These women will receive the current recommendations of the government of Sierra Leone, which includes standard intermittent preventive treatment of malaria during pregnancy (IPTp) of 2 doses of sulfadoxine/ pyrimethamine, iron and folic acid supplement with a goal of 90 pills/pregnancy, an insecticide-treated mosquito net, and albendazole for deworming in the second trimester.
Intervention Type
Dietary Supplement
Intervention Name(s)
Ready-to-use-supplementary food
Intervention Description
Specially formulated supplementary food for pregnancy
Intervention Type
Dietary Supplement
Intervention Name(s)
Corn-soy-blend
Intervention Description
Standard of care for malnutrition in pregnancy in Sierra Leone
Intervention Type
Drug
Intervention Name(s)
Monthly intermittent preventive treatment of malaria during pregnancy (IPTp)
Other Intervention Name(s)
Sulfadoxine-pyrimethamine
Intervention Description
Sulfadoxine-pyrimethamine (500 mg / 25 mg) given every 4 weeks, beginning at enrollment or at 13 weeks' gestation, whichever is later.
Intervention Type
Drug
Intervention Name(s)
Standard intermittent preventive treatment of malaria during pregnancy (IPTp)
Other Intervention Name(s)
Sulfadoxine-pyrimethamine
Intervention Description
Standard of care for Sierra Leone is 2 doses of sulfadoxine/ pyrimethamine (500mg/ 25mg).
Intervention Type
Other
Intervention Name(s)
Insecticide-treated mosquito net
Intervention Description
An insecticide-treated mosquito net at the time of enrollment into the study.
Intervention Type
Drug
Intervention Name(s)
Azithromycin
Intervention Description
Azithromycin 1 gram given once in second trimester and again during weeks 28-34 of gestation.
Intervention Type
Drug
Intervention Name(s)
Albendazole
Intervention Description
Single dose albendazole 400mg given in the second trimester.
Intervention Type
Combination Product
Intervention Name(s)
Bacterial vaginosis testing and treatment
Intervention Description
Testing for bacterial vaginosis at enrollment and again at weeks 28-34 using a rapid diagnostic test for sialidase. Those with positive tests will receive extended release metronidazole 750mg daily for 7 days.
Primary Outcome Measure Information:
Title
Infant birth length
Description
mean birth length of infants born to mothers in the study
Time Frame
up to 40 weeks
Secondary Outcome Measure Information:
Title
Maternal weight gain
Description
Average weekly weight gain of women in the study
Time Frame
up to 40 weeks
Title
Proportion recovered from maternal malnutrition
Description
proportion of women who reach mid-upper-arm circumference (MUAC) > 23 cm
Time Frame
up to 40 weeks
Title
Premature delivery
Description
proportion of infants born prematurely
Time Frame
up to 36 weeks
Title
Newborn head circumference
Description
mean head circumference of infants born to women in the study
Time Frame
up to 40 weeks
Title
Infant birth weight
Description
mean birth weights of infants born to mothers in the study
Time Frame
up to 40 weeks
Title
Infant weight at 6 weeks, 3 and 6 months
Description
infant ponderal growth
Time Frame
up to 6 months
Title
Infant length at 6 weeks, 3 and 6 months
Description
infant linear growth
Time Frame
up to 6 months
Title
Infant survival at 3 and 6 months
Description
survival of infants in the study
Time Frame
up to 6 months

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Must be pregnant woman
Minimum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Pregnant women and consenting to study participation Fundal height not greater than 32 cm Mid-upper arm circumference ≤23 cm Planning to reside in the study area during pregnancy and 6 months post partum Attending 1 of the 40 antenatal clinic sites Exclusion Criteria: < 16 years of age without adult willing to consent Known pregnancy complications such as gestational diabetes, pre-eclampsia, hypertension
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark J Manary, MD
Organizational Affiliation
Washington University School of Medicine
Official's Role
Study Chair
Facility Information:
Facility Name
1 Moriba Street
City
Pujehun
State/Province
Pujehun District
Country
Sierra Leone

12. IPD Sharing Statement

Citations:
PubMed Identifier
34582451
Citation
Hendrixson DT, Smith K, Lasowski P, Callaghan-Gillespie M, Weber J, Papathakis P, Iversen PO, Koroma AS, Manary MJ. A novel intervention combining supplementary food and infection control measures to improve birth outcomes in undernourished pregnant women in Sierra Leone: A randomized, controlled clinical effectiveness trial. PLoS Med. 2021 Sep 28;18(9):e1003618. doi: 10.1371/journal.pmed.1003618. eCollection 2021 Sep.
Results Reference
derived
PubMed Identifier
32153879
Citation
Hendrixson DT, Koroma AS, Callaghan-Gillespie M, Weber J, Papathakis P, Manary MJ. Use of a novel supplementary food and measures to control inflammation in malnourished pregnant women in Sierra Leone to improve birth outcomes: study protocol for a prospective, randomized, controlled clinical effectiveness trial. BMC Nutr. 2018 Apr 2;4:15. doi: 10.1186/s40795-018-0218-y. eCollection 2018.
Results Reference
derived

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Nutritional and Anti-infective Interventions for Malnutrition in Pregnancy (Beleuman Welbodi)

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