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NCT06483997

Associations Between Diet, Hepcidin, and Relative Dose Intensity Among Women Receiving Chemotherapy for Breast or Gynecological Cancer

Active, enrolled Last updated 27 January 2026
What this trial tests

trial in Breast Cancer Female in 100 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
16 August 2024
Primary endpoint
1 July 2026
1 July 2026

Quick facts

Lead sponsorGeorge Washington University
StatusActive, enrolled
Study typeOBSERVATIONAL
Enrollment100
Start date16 August 2024
Primary completion1 July 2026
Estimated completion1 July 2026
Sites1 location across United States

Conditions studied

Sponsor

George Washington University

Who can join

21 and older, female only, with Breast Cancer Female or Ovarian Cancer. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

This prospective, observational cohort study will evaluate the extent of associations between self-reported pro- or anti- inflammatory dietary intake patterns for one month before induction chemotherapy for gynecological cancer or neo/adjuvant chemotherapy for breast cancer and baseline serum hepcidin concentrations. Associations between hepcidin concentration and relative dose intensity (RDI) of chemotherapy will also be evaluated.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Antimicrobial peptides: from discovery to developmental applications.
    Zhang Q. · · 2025 · cited 20× · PMID 40178173 · DOI 10.1128/aem.02115-24

Verify or expand the search:

Other recruiting trials for Breast Cancer Female

Currently open trials in the same condition.

Other George Washington University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06483997.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing