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The Immediate and Long-term Effects of a Novel Marine-based Iron Supplement in Adult Females

NCT07199244 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 61

Last updated 2025-09-30

No results posted yet for this study

Summary

The goal of this study is to identify how well a fish-based iron supplement is absorbed and to learn how many, if any, digestive related side effects are caused by ingesting the supplement.

Conditions

  • Anemia
  • Iron Deficiency (Without Anemia)
  • Iron Absorption

Interventions

DIETARY_SUPPLEMENT

marine-based heme iron

Participants will consume 9mg of SalmoFer on day 1, followed by 6mg each day for 56 days.

Sponsors & Collaborators

  • Nutraceuticals Research Institute

    lead OTHER

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Max Age
42 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-08-01
Primary Completion
2025-05-31
Completion
2025-10-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT07199244 on ClinicalTrials.gov