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Effectiveness Trial of Locally Developed Ready to Use Therapeutic Food

Primary Purpose

Malnutrition Severe

Status
Not yet recruiting
Phase
Not Applicable
Locations
Bangladesh
Study Type
Interventional
Intervention
Sharnali 1
Sharnali 2
Sponsored by
International Centre for Diarrhoeal Disease Research, Bangladesh
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Malnutrition Severe focused on measuring Severe Acute Malnutrition, Local RUTF, Effectiveness Trial, Forcibly Displaced Myanmar Nationals, Bangladesh

Eligibility Criteria

6 Months - 59 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Severe acute malnourished children
  • Age 6-59 months
  • Either sex
  • No medical complication
  • MUAC <115 mm and/or WLZ/WHZ <-3.

Exclusion Criteria:

  • Children not suffering from severe acute malnutrition
  • Children with oedematous malnutrition
  • Failed to obtain consent for study participation from parents or legal guardian
  • Suffering from any chronic illness(es) etc.

Sites / Locations

  • International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b)
  • International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b)

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

To provide Sharnali-1 to severe acute malnourished children

To provide Sharnali-2 to severe acute malnourished children

Arm Description

We will provide Sharnali-1 among 225 severe acute malnourished children to assess the proportion of children graduating from SAM to non-acute malnutrition status (MUAC ≥ 125 mm or WLZ/WHZ ≥ -2 for two consecutive weeks) by 90 days of intervention.

We will provide Sharnali-2 among 225 severely acute malnourished children to assess the proportion of children graduating from SAM to non-acute malnutrition status (MUAC ≥ 125 mm or WLZ/WHZ ≥ -2 for two consecutive weeks) by 90 days of intervention.

Outcomes

Primary Outcome Measures

Proportion of children graduating from SAM to non-acute malnutrition status
The primary outcome variable is to assess the proportion of children graduating from SAM to non-acute malnutrition status (MUAC ≥ 125 mm or WLZ/WHZ ≥ -2 for two consecutive weeks) by 90 days of intervention

Secondary Outcome Measures

Time (days) required to graduate from SAM to non-acute malnutrition status
Required Time for graduation from SAM to non acute malnutrition measured in days
Rate of weight gain of children (g/kg per day) during 1st 2 weeks, 1st 4 weeks and up to graduation
Children's weight gain measured as g/kg/day
Proportion of children recovered (MUAC ≥ 125 mm or WLZ/WHZ ≥ -2) by different time periods
Proportion of recovery at different time points measured as percentage
Changes in weight
Changes in body weight measured in kg
Changes in Mid Upper Arm Circumference (MUAC)
Changes in Mid Upper Arm Circumference (MUAC) measured in mm or cm
Changes in height
Changes in height measured in cm
Changes in weight-for-height Z score
Changes in weight-for-height Z score measured in points
Changes in weight-for-age Z score
Changes in weight-for-age Z score measured in points
Changes in height-for-age Z score
Changes in height-for-age Z score measured in points
Proportion of children dropped out
Proportion of children dropped out measured in percentage
Proportion of children relapsed (deterioration of weight, appearance of edema or any clinical emergencies)
Proportion of children relapsed (deterioration of weight, appearance of edema or any clinical emergencies) measured in percentage
Proportion of children needed hospital admission after enrolment
Proportion of children needed hospital admission after enrolment measured in percentage

Full Information

First Posted
May 19, 2022
Last Updated
December 19, 2022
Sponsor
International Centre for Diarrhoeal Disease Research, Bangladesh
Collaborators
UNICEF
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1. Study Identification

Unique Protocol Identification Number
NCT05520879
Brief Title
Effectiveness Trial of Locally Developed Ready to Use Therapeutic Food
Official Title
Community-based Management of Acute Malnutrition (CMAM) in Bangladesh: Effectiveness Trial of Locally Developed Ready-to-use Therapeutic Food in the Treatment of Severe Acute Malnutrition in Rohingya Camps in Cox's Bazar
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
January 1, 2023 (Anticipated)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
December 31, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
International Centre for Diarrhoeal Disease Research, Bangladesh
Collaborators
UNICEF

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
As poor health conditions and malnutrition are major issues confronting the influx of Forcibly Displaced Myanmar Nationals (FDMN), there is an urgent need to prepare the service providers to control the situation and to prevent deaths and disabilities in FDMN children suffering from severe acute malnutrition (SAM). It is therefore imperative to assess the effectiveness of the two local Nutrition Managements (NMs); Sharnali 1 & Sharnali 2 for the treatment of SAM in an emergency in Bangladesh. If the effectiveness trial shows that the NMs are effective, either one or both varieties can be used for children with SAM in emergency situations. Ultimately a Bangladeshi solution will replace the expensive RUTF that is currently being imported for use in the FDMN camps for management of SAM.
Detailed Description
In response to the huge global burden of childhood acute malnutrition, WHO and UNICEF have recommended since 2007 ready-to-use therapeutic food (RUTF) as the treatment for children with severe acute malnutrition (SAM) without complications in the community. Although there is no national program in Bangladesh for management of SAM in the community, the Ministry of Health and Family Welfare (MoHFW) has posited for a therapeutic food to manage childhood malnutrition that is made of locally available food ingredients. With this backdrop, icddr,b developed two types of such food called Nutritional Management (NM) for the management of uncomplicated SAM in the community. These NMs conform to the National Guidelines on Community-based Management of SAM of the Government of Bangladesh as well as WHO and UNICEF specifications. These newly developed therapeutic foods, named as Sharnali-1 and Sharnali-2, are made of locally available food ingredients including rice, lentils, and chickpeas respectively and a recently conducted trial assessing their acceptability among SAM children showed that the local Bangladeshi NMs are as acceptable as the imported RUTF (Annex1: Composition of the locally developed NMs). Same group of researchers also completed a randomized, double-blind efficacy trial among children with SAM in Dhaka and in Kurigram that revealed that the local NMs are as efficacious as the imported RUTF. Poor health conditions and malnutrition are major issues confronting the influx of about 1000,000 Forcibly Displaced Myanmar Nationals (FDMN; the FDMN people from across the border into Bangladesh). It is unfortunately anticipated that the deadliest form of malnutrition - severe acute malnutrition (SAM) - will greatly exceed the current national prevalence as a result of severe food insecurity, disease, and the existing high levels of malnutrition among those who are crossing the border. There is an urgent need to prepare ourselves to control the situation and to prevent deaths and disabilities in refugee children suffering from SAM. It is therefore imperative to assess the effectiveness of the two local NMs for the treatment of SAM in an emergency situation in Bangladesh, the FDMN situation being one that demands urgent attention. If the effectiveness trial shows that the NMs are effective, either one or both varieties can be used for children with SAM in emergency situations where food insecurity is extreme. Ultimately, a Bangladeshi solution will replace the expensive RUTF that is currently being imported for use in the FDMN FDMN camps. On the other hand, researchers also want to explore their perception, belief and practices if NMs and RUTF in that community is being provided. Unexpectedly, there is no data available on how they perceive about SAM management and how they would response if the above mentioned services are implemented. Therefore, the researchers would like to explore maternal/caregiver perception, knowledge, practices and barriers towards community-based health care management among FDMN population as well. The Ministry of Health and Family Welfare of Bangladesh has approved conduction of the trial of the local therapeutic foods, Sharnali-1 and Sharnali-2, developed by icddr,b among under-five children in FDMN Forcibly Displaced Myanmar National (FDMN) camps suffering from SAM. Objectives: To assess the effectiveness of two local NMs (Sharnali-1 and Sharnali-2) in managing 6-59 months old children suffering from SAM in the community in an emergency setting (for example, the Camps of Forcibly Displaced Myanmar Nationals). Methods: An effectiveness trial will be conducted using the Bangladeshi NMs in the FDMN Camps in Teknaf and Ukhiya sub-districts of Cox's Bazar district. The primary outcome variable of the effectiveness trial is to assess the proportion of children graduating from SAM to non-acute malnutrition status (MUAC ≥ 125 mm or WLZ/WHZ ≥ -2 for two consecutive weeks) by 90 days of intervention. The total number of participants enrolled for the effectiveness trial would be 450 children with SAM in two arms.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Malnutrition Severe
Keywords
Severe Acute Malnutrition, Local RUTF, Effectiveness Trial, Forcibly Displaced Myanmar Nationals, Bangladesh

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Sharnali-1 and Sharnali-2 would be provided among 450 severely acute malnourished children divided into two groups to assess the proportion of children graduating from SAM to non-acute malnutrition status (MUAC ≥ 125 mm or WLZ/WHZ ≥ -2 for two consecutive weeks) by 90 days of intervention.
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
The intervention study products will be packaged in sachets that cannot be differentiated between the two.
Allocation
Randomized
Enrollment
450 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
To provide Sharnali-1 to severe acute malnourished children
Arm Type
Experimental
Arm Description
We will provide Sharnali-1 among 225 severe acute malnourished children to assess the proportion of children graduating from SAM to non-acute malnutrition status (MUAC ≥ 125 mm or WLZ/WHZ ≥ -2 for two consecutive weeks) by 90 days of intervention.
Arm Title
To provide Sharnali-2 to severe acute malnourished children
Arm Type
Experimental
Arm Description
We will provide Sharnali-2 among 225 severely acute malnourished children to assess the proportion of children graduating from SAM to non-acute malnutrition status (MUAC ≥ 125 mm or WLZ/WHZ ≥ -2 for two consecutive weeks) by 90 days of intervention.
Intervention Type
Dietary Supplement
Intervention Name(s)
Sharnali 1
Intervention Description
The intervention is food product, made from locally available food ingredients in Bangladesh. Sharnali 1 made from rice, lentil, dried skimmed milk, sugar, vegetable oils and micronutrient premix.
Intervention Type
Dietary Supplement
Intervention Name(s)
Sharnali 2
Intervention Description
Sharnali 2 made from chick peas, dried skimmed milk, sugar, vegetable oils and micronutrient premix.
Primary Outcome Measure Information:
Title
Proportion of children graduating from SAM to non-acute malnutrition status
Description
The primary outcome variable is to assess the proportion of children graduating from SAM to non-acute malnutrition status (MUAC ≥ 125 mm or WLZ/WHZ ≥ -2 for two consecutive weeks) by 90 days of intervention
Time Frame
90 days
Secondary Outcome Measure Information:
Title
Time (days) required to graduate from SAM to non-acute malnutrition status
Description
Required Time for graduation from SAM to non acute malnutrition measured in days
Time Frame
90 days
Title
Rate of weight gain of children (g/kg per day) during 1st 2 weeks, 1st 4 weeks and up to graduation
Description
Children's weight gain measured as g/kg/day
Time Frame
90 days
Title
Proportion of children recovered (MUAC ≥ 125 mm or WLZ/WHZ ≥ -2) by different time periods
Description
Proportion of recovery at different time points measured as percentage
Time Frame
90 days
Title
Changes in weight
Description
Changes in body weight measured in kg
Time Frame
90 days
Title
Changes in Mid Upper Arm Circumference (MUAC)
Description
Changes in Mid Upper Arm Circumference (MUAC) measured in mm or cm
Time Frame
90 days
Title
Changes in height
Description
Changes in height measured in cm
Time Frame
90 days
Title
Changes in weight-for-height Z score
Description
Changes in weight-for-height Z score measured in points
Time Frame
90 days
Title
Changes in weight-for-age Z score
Description
Changes in weight-for-age Z score measured in points
Time Frame
90 days
Title
Changes in height-for-age Z score
Description
Changes in height-for-age Z score measured in points
Time Frame
90 days
Title
Proportion of children dropped out
Description
Proportion of children dropped out measured in percentage
Time Frame
90 days
Title
Proportion of children relapsed (deterioration of weight, appearance of edema or any clinical emergencies)
Description
Proportion of children relapsed (deterioration of weight, appearance of edema or any clinical emergencies) measured in percentage
Time Frame
90 days
Title
Proportion of children needed hospital admission after enrolment
Description
Proportion of children needed hospital admission after enrolment measured in percentage
Time Frame
90 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
6 Months
Maximum Age & Unit of Time
59 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Severe acute malnourished children Age 6-59 months Either sex No medical complication MUAC <115 mm and/or WLZ/WHZ <-3. Exclusion Criteria: Children not suffering from severe acute malnutrition Children with oedematous malnutrition Failed to obtain consent for study participation from parents or legal guardian Suffering from any chronic illness(es) etc.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Salam Khan
Phone
+880-2-9827001-10
Ext
3206
Email
salamk@icddrb.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Md Munirul Islam, PhD
Organizational Affiliation
Scientist
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Nurun Nahar Naila, MPH
Organizational Affiliation
Assistant Scientist
Official's Role
Principal Investigator
Facility Information:
Facility Name
International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b)
City
Teknāf
State/Province
Cox's Bazar
Country
Bangladesh
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Md Munirul Islam, PhD
Email
mislam@icddrb.org
First Name & Middle Initial & Last Name & Degree
Mahabub Uz Zaman
Email
lumen@icddrb.org
Facility Name
International Centre for Diarrhoeal Disease Research, Bangladesh (icddr,b)
City
Ukhiya
State/Province
Cox's Bazar
Country
Bangladesh
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Md Munirul Islam, PhD
Phone
8801713006878
Email
mislam@icddrb.org
First Name & Middle Initial & Last Name & Degree
Mahabub Uz Zaman
Email
lumen@icddrb.org

12. IPD Sharing Statement

Plan to Share IPD
No

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Effectiveness Trial of Locally Developed Ready to Use Therapeutic Food

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