Phase 1 Seattle Dietary Biomarkers Development Center

NCT05580653 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2026-02-20

No results posted yet for this study

Summary

The Seattle Dietary Biomarker Development Center (S-DBDC) aims to advance the science of measuring dietary intake by identification and validation of dietary biomarkers that improve upon self-reported diet. To accomplish this mission, the Seattle DBDC will carry out controlled feeding studies in healthy human volunteers. Metabolomics assays will be conducted on blood and urine specimens collected during the feeding studies for biomarker identification.

Conditions

  • Healthy Adults

Interventions

OTHER

Controlled feeding study of beef and/or pinto beans

Crossover feeding study of three, 7-day feeding periods with plant and/or animal proteins (beef, pinto beans, and half beef/half pinto beans) completed in random order.

OTHER

Controlled feeding study of eggs and/or black beans

Crossover feeding study of three, 7-day feeding periods with plant and/or animal proteins (eggs, black beans, and half eggs/half black beans) completed in random order.

Sponsors & Collaborators

  • United States Department of Agriculture - National Institute of Food and Agriculture (USDA-NIFA)

    collaborator UNKNOWN
  • University of Nebraska

    collaborator OTHER
  • University of Washington

    collaborator OTHER
  • Duke University

    collaborator OTHER
  • Marian Neuhouser

    lead OTHER

Principal Investigators

  • Marian L. Neuhouser, PhD, RD · Fred Hutchinson Cancer Center

  • Johanna W. Lampe, PhD, RD · Fred Hutchinson Cancer Center

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-03-02
Primary Completion
2025-04-17
Completion
2025-04-17

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05580653 on ClinicalTrials.gov