NCT06184984

Brief Summary

The goal of this study is to determine the protein quality of Philippine mung beans. The main objective of this study is to determine the metabolic availability of methionine in mung beans that the body can use. We will test the mung beans by studying them after cooking them as sauté. This research is being done in order to bridge the gap between knowledge of protein requirement and the amount of food needed to meet that requirement. Results from this study will be important for recommendations guiding food choices of mung beans as a major protein source in the diet. Each study participant will be part of seven (7) different experimental diets, and randomly assigned to one of the diets every time. Four (4) reference diets would be based on egg protein composition, and three (3) test diets will have protein from cooked mung beans. Each experimental diet will be studied over 3 days: 2 adaptation days and 1 study day. The meals during the 2-day adaptation period would be consumed at home. On the study day, following a 10 to 12-h overnight fast, the study participants will come to the research unit at the Department of Science - Food and Nutrition Research Institute (DOST-FNRI), Gen. Santos Ave., Bicutan, Taguig City, Philippines, for a period of 8 to 9 hours and consume the diets as 9 hourly meals.

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
6

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Apr 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

December 14, 2023

Completed
15 days until next milestone

First Posted

Study publicly available on registry

December 29, 2023

Completed
1.3 years until next milestone

Study Start

First participant enrolled

April 1, 2025

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2025

Completed
Last Updated

February 13, 2025

Status Verified

October 1, 2024

Enrollment Period

8 months

First QC Date

December 14, 2023

Last Update Submit

February 11, 2025

Conditions

Keywords

Metabolic AvailabilityMethionineIAAOMung beans

Outcome Measures

Primary Outcomes (1)

  • Metabolic availability of methionine in mung beans

    Protein quality of mung beans measured as metabolic availability using the IAAO method

    2 years

Study Arms (1)

Methionine metabolic availability in mung beans

EXPERIMENTAL

Participants will be seen initially for pre-study assessment. They will then be studied for up to 7 times. The participants will be expected to participate in 7 different sets of experiments which will take 2 to 3 months. Each set of experiment consists of a 3 day period. During the first 2 days (Adaptation Days) you will be expected to consume 4 meals per day consisting of a protein liquid drink and protein free-cookies and/or cooked mung bean, which will be provided by the investigators.

Dietary Supplement: Metabolic availability of methionine in mung beans

Interventions

Each participant will randomly receive 7 different levels of methionine provided as free amino acids and cooked mung beans.

Methionine metabolic availability in mung beans

Eligibility Criteria

Age19 Years - 40 Years
Sexfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Non-pregnant
  • Non-lactating
  • Stable body weight
  • Healthy, with no known clinical condition that would affect protein or AA metabolism, e.g. Diabetes
  • Not on any medications that could affect protein or amino acid metabolism e.g. steroids.

You may not qualify if:

  • Unwillingness to participate or unable to tolerate the diet
  • Recent history of weight loss within the last 3 months or on a weight-reducing diet
  • Inability to tolerate study diets (e.g. Allergy to ingredients)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Department of Science and Technology - Food and Nutrition Research Institute

City of Taguig, National Capital Region, 1630, Philippines

Location

Study Officials

  • Johanne B Guilaran, Bachelor's

    Department of Science and Technology - Food and Nutrition Research Institute

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Johanne B Guilaran, Bachelor's

CONTACT

Ma. Lourdes T Cumagun, Bachelor's

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER GOV
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

December 14, 2023

First Posted

December 29, 2023

Study Start

April 1, 2025

Primary Completion

December 1, 2025

Study Completion

December 1, 2025

Last Updated

February 13, 2025

Record last verified: 2024-10

Data Sharing

IPD Sharing
Will not share

Locations