Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02847962
Other study ID # FFE-621-2012/033-00
Secondary ID
Status Completed
Phase N/A
First received July 20, 2016
Last updated July 25, 2016
Start date February 2016

Study information

Verified date July 2016
Source Kansas State University
Contact n/a
Is FDA regulated No
Health authority United States: Institutional Review BoardTanzania and United States: Project Concern InternationalTanzania: National Institute for Medical Research
Study type Interventional

Clinical Trial Summary

Corn-soy vitamin and mineral fortified blended foods (FBFs) are primarily used for food aid, although sorghum and cowpea may be suitable alternative FBF commodities. The objective of the Micronutrient Fortified Food Aid Pilot Project (MFFAPP) Tanzania Efficacy Study is to determine whether newly formulated, extruded sorghum- and cowpea-based FBFs have equal, or better, nutritive value and acceptance compared to a traditional corn-soy blend. The effectiveness of each blend will be determined in an efficacy study of Tanzanian children under the age of 5 that are deficient, or at risk for deficiency, in iron and vitamin A.


Recruitment information / eligibility

Status Completed
Enrollment 2179
Est. completion date
Est. primary completion date July 2016
Accepts healthy volunteers No
Gender Both
Age group 6 Months to 53 Months
Eligibility Inclusion Criteria:

- Hemoglobin <10.3mg/dl

- Weight-for-height z-scores >-3

Exclusion Criteria:

- Exclusive breastfeeding

- Unwillingness to travel to health facilities

- Enrollment of child in school during study period

- Anticipated relocation of the family during the study

- Allergy to the fortified-blended food product ingredients

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Other:
Corn Soy Blend Plus (CSB+)

Corn Soy Blend 14 (CSB14)

White Sorghum Cowpea Blend Variety 1

White Sorghum Cowpea Blend Variety 2

Red Sorghum Cowpea Blend

White Sorghum Soy Blend


Locations

Country Name City State
n/a

Sponsors (4)

Lead Sponsor Collaborator
Kansas State University National Institute for Medical Research, Tanzania, Project Concern International - Tanzania, United States Department of Agriculture Foreign Agricultural Service

Outcome

Type Measure Description Time frame Safety issue
Primary Hemoglobin Change 0, 10, 20 weeks (baseline, midline, and end line) No
Primary Dried blood spot retinol binding protein change Assessment of vitamin A status 0, 10, 20 weeks (baseline, midline, and end line) No
Secondary Height-for-age change 0, 10, 20 weeks (baseline, midline, and end line) No
Secondary Weight-for-age change 0, 10, 20 weeks (baseline, midline, and end line) No
Secondary Weight-for-height change 0, 10, 20 weeks (baseline, midline, and end line) No
Secondary Moderate malnutrition status change Weight-for-age between -3 and -2 z-scores below the median of the WHO child growth standards 0, 10, 20 weeks (baseline, midline, and end line) No
Secondary Mid-upper arm circumference change 0, 10, 20 weeks (baseline, midline, and end line) No
See also
  Status Clinical Trial Phase
Active, not recruiting NCT03516734 - Iron-fortified Lentils to Improve Iron (Fe) Status in Bangladesh N/A
Completed NCT02570854 - A Two-part Single- and Repeat-dose Study of CSJ137 in Anemic Chronic Hemodialysis Patients Phase 1
Completed NCT02887963 - Epidemiological Study of Iron Deficiency and Iron Deficiency Anemia in Chinese Pregnant Women N/A
Completed NCT00534144 - Comparison Between Effects of Two Iron Preparations on Protein in the Urine Phase 1
Completed NCT00224081 - DRIVE Trial (Dialysis Patients' Response to Intravenous [IV] Iron With Elevated Ferritin) Phase 4
Recruiting NCT02999217 - Intravenous Iron for Correction of Anaemia After Colorectal Surgery Phase 4
Recruiting NCT04351607 - Preoperative Supplementation of Sucrosomal Iron as Hematopoietic Support. N/A
Completed NCT04163406 - The Effect of Human Milk Oligosaccharides and Galacto-oligosaccharides on Iron Absorption in Kenyan Infants N/A
Completed NCT02365103 - Tea Consumption and Iron Bioavailability in Women Using a Stable Isotope N/A
Completed NCT00536666 - A Study of Iron Oligosaccharide in Chronic Kidney Disease Patients Phase 3
Completed NCT02310607 - Non-invasive Optical Detection of Iron Deficiency N/A
Completed NCT01755455 - Does a Daily Iron Tablet Improve Anemia in Cystic Fibrosis N/A
Terminated NCT00929409 - Controlled Randomised Trial of Ferric Carboxymaltose and Oral Iron to Treat Postpartum Anemia Phase 2/Phase 3
Completed NCT00354692 - Effect of Two Iron Preparations on Protein in the Urine Phase 4
Recruiting NCT05628896 - Efficacy of a Preoperative Anaemia Clinic in Patients Undergoing Elective Abdominal Surgery
Completed NCT02905539 - A Study Comparing the Iron Substitution With the Medicinal Products Ferinject or Monofer Phase 4
Completed NCT02892461 - Effect of Umbilical Cord Milking on Iron Related Health Outcomes for Cesarean-Delivered Infants N/A
Not yet recruiting NCT01840384 - Efficacy Study of Multiple Micro Nutrients Supplementation N/A
Recruiting NCT00125996 - Effect of Intravenous Ferrous Sucrose on Exercise Capacity in Chronic Heart Failure Phase 1/Phase 2
Not yet recruiting NCT04975074 - Iron Deficiency Anemia in Twin Pregnancies Phase 4