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Modified Dosage for Moderate Acute Malnutrition (MODAM-MAM)

Study acronym: MODAM-MAM
StatusUnknown
PhaseNot applicable
Started
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Record status
This record was last updated July 16, 2024 (before its estimated September 25, 2026 completion). Its status may not reflect the trial's current state.

Record History

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  1. Minor Changed Registry marked status Unknown (sponsor has not verified the record since Jul 2024); last known: Recruiting
  2. Notable Trial status: Not Yet Recruiting to Recruiting
    • Study sites: 0 to 3
    • Interventions: Amoxicillin (Drug), ready-to-use supplementary food (RUSF) (Dietary Supplement), ready-to-use therapeutic food (RUTF) (Dietary Supplement) to ready-to-use supplementary food (RUSF) (Dietary Supplement), ready-to-use therapeutic food (RUTF) (Dietary Supplement)
    • Eligibility criteria shortened, about 7 words
    v2
  3. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Protocols for the community-based management of acute malnutrition (CMAM) have not changed significantly for more than 20 years, with relatively complex treatment protocols and persistent supply chain challenges that have limited overall program coverage, leaving millions of malnourished children without care annually. The overarching goal of this research project is to simultaneously test two novel simplified approaches in CMAM with potential to improve program coverage. The simplified approach includes two parallel clinical trials for SAM and MAM treatment. Two fixed-dose regimes of RUTF will be tested against the current fixed-dose regimen of RUSF for children with MAM.
Trial Details
NCT Number NCT06056089
Lead Sponsor Action Against Hunger USA
Collaborators: University of Washington, Ethiopian Public Health Institute
Conditions
(from sponsor)
Moderate Acute Malnutrition
Enrollment 2,400 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov