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A single-center, single-arm clinical trial to evaluate the efficacy of Liaoshen roe nanoactive peptide functional drink in women with diminished ovarian function

A single-center, single-arm clinical trial to evaluate the efficacy of Liaoshen roe nanoactive peptide functional drink in women with diminished ovarian function

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128717
Enrollment
Unknown
Registered
2026-07-24
Start date
2026-01-13
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diminished ovarian function

Interventions

experimental group:Liaoshen Sea Cucumber Egg Nano Active Peptide Drink 25mL/bottle 1 bottle per time, once a day

Sponsors

Shengjing Hospital Affiliated to China Medical University.
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
35 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Females aged 35-50 years with a body mass index (BMI) of 18.5-28 kg/m^2; 2. Oligomenorrhea or amenorrhea for 4 months to 1 year; 3. Serum basal follicle-stimulating hormone (FSH) >= 10 U/L (measured at least twice, with an interval of > 4 weeks between tests). Measurements should be performed on days 2-4 of the menstrual cycle, or at any time in cases of amenorrhea. Serum anti-Müllerian hormone (AMH) <= 1.1 ng/mL; 4. Pelvic ultrasonography findings: (1) Normal or slightly reduced uterine size; (2) Bilaterally small ovaries or poorly visualized ovaries; (3) Total number of antral follicles (2-10 mm in diameter) in both ovaries < 5, or absence of visible follicles; 5. All participants must be married and have a normal sexual life; 6. Voluntary participation in the clinical trial, good compliance, and provision of written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with ovarian tumors, endometriosis, or other neoplastic diseases. 2. History of pelvic surgery. 3. Presence of thrombotic disorders or hematological diseases. 4. Severe infection or severe inflammatory response. 5. Cognitive or communication disorders that may interfere with study participation. 6. Cardiac, hepatic, pulmonary, or renal insufficiency. 7. Thyroid dysfunction or other endocrine disorders. 8. Recent use of estrogen- or progesterone-containing medications. 9. Amenorrhea due to causes other than diminished ovarian function (e.g., primary amenorrhea, uterine amenorrhea, pituitary amenorrhea), as well as women who are preparing for pregnancy or breastfeeding. 10. Any other condition that, in the investigator’s judgment, makes the subject unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Anti-Müllerian Hormone(AMH);Follicle-Stimulating Hormone(FSH);Luteinizing Hormone;Estradiol;Progesterone;Testosterone;Prolactin;

Countries

China

Contacts

Public ContactBing He

Shengjing Hospital Affiliated to China Medical University

hebing7557@163.com+86 189 4025 9707

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026