The Efficacy of Minayo Iron-rich Nutritional Gummies on Female Anemia, Skin Condition and Qi-blood Deficiency Syndrome

Last updated: July 1, 2025
Sponsor: Hangzhou Agile Groups Network Technology Co., Ltd.
Overall Status: Completed

Phase

N/A

Condition

Anemia

Treatment

Common Gummies

Minayo Iron-rich Nutritional Gummies

Clinical Study ID

NCT06869824
25-RD-01-MY-001
  • Ages 18-45
  • Female
  • Accepts Healthy Volunteers

Study Summary

The goal of this randomized, double-blind, placebo controlled study is to learn about the efficacy of Minayo Iron-rich Nutritional Gummies on females who are aged 18-45 and suffer nutritional Anemia, skin condition and Qi-blood deficiency syndrome. The main question it aims to answer is:

  • whether the Anemia (measured by serum ferritin level and hemoglobin concentration Level in blood) is improved after the intervention

36 qualified participants will be enrolled and assigned to two equal-size groups with study product (Minayo Iron-rich Nutritional Gummies) and placebo product (common gummies) in one study center in Shanghai. The study will last 4 weeks and three site visits will be made, during which all clinical data will be captured and entered to EDC system for statistical analysis and reporting.

Researchers will find out whether the study product (Minayo Iron-rich Nutritional Gummies) is effective to improve Anemia, skin conditions, and Qi-blood deficiency symptoms by comparing the two groups.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Female subjects, aged 18 to 45;

  • 36 young women with mild anemia (hemoglobin value between 90-110 g/l) were recruitedbased on WHO diagnostic criteria for anemia. 10 of the subjects always have coffeeand milk tea more than once per day;

  • Participants agree not to take any drugs, supplements, or other dairy productsduring the trial;

  • Participants agree not to take any other medications or supplements containing ironduring the trial;

  • Antibiotics may be used unless medically required, but the type and dosage and daystaken should be recorded;

  • Willing to refrain from participating in other interventional clinical studiesduring the trial period;

  • Fully understand the nature, purpose, benefits and possible risks and side effectsof the study;

  • Willing to obey all test requirements and procedures;

  • Sign informed consent form.

Exclusion

Exclusion Criteria:

  • Anemia due to organic conditions;

  • Subject who is in the treatment of gastrointestinal symptoms;

  • Lactose intolerance;

  • Subject who is currently presence of other organic diseases affecting intestinalfunction, such as history of gastrointestinal resection, colon or rectal cancer,inflammatory bowel disease, diabetes, hyperthyroidism or hypothyroidism, congenitalmegacolon, scleroderma, anorexia nervosa, etc.;

  • Controlling diet, exercising, or taking medications to control weight or affectappetite in the last 3 months;

  • Subject who has any of the following medical history or clinical findings that mayaffect the evaluation of the trial effect: significant gastrointestinal disorders,liver, kidney, endocrine, hematological, respiratory and cardiovascular diseases;

  • Abuse alcohol or other drugs, supplement or OTC drugs currently or in the past maycause bowel dysfunction or can affect test result evaluation;

  • Frequently use of medications that may affect gastrointestinal function or theimmune system according to investigator's judgment;

  • Take laxatives or other substances that promote digestion 2 weeks before the trailstart;

  • Subject who used drugs or supplements of iron agent 10 days before the beginning ofthe trial;

  • Pregnant or lactating women or those planning to become pregnant during the trial;

  • PI deems that subjects could not fully cooperate with trial arrangements.

Study Design

Total Participants: 36
Treatment Group(s): 2
Primary Treatment: Common Gummies
Phase:
Study Start date:
March 17, 2025
Estimated Completion Date:
April 13, 2025

Connect with a study center

  • Shanghai Raison CMA Lab

    Shanghai, Shanghai
    China

    Site Not Available

Not the study for you?

Let us help you find the best match. Sign up as a volunteer and receive email notifications when clinical trials are posted in the medical category of interest to you.