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Human Clinical Trial of OVAREVIVE II™ for Improving Symptoms of Diminished Ovarian Reserve

Human Clinical Trial of OVAREVIVE II™ for Improving Symptoms of Diminished Ovarian Reserve

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500096965
Enrollment
Unknown
Registered
2025-02-10
Start date
2025-02-10
Completion date
Unknown
Last updated
2025-02-17

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

Conditions

?Diminished Ovarian Reserve (DOR)??12.

Interventions

test group:taking OVAREVIVE II

Sponsors

?Zhejiang Hospital??
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
25 Years to 50 Years

Inclusion criteria

Inclusion criteria: (1)The age of the subjects should be between 25 and 50 years old (inclusive); (2)Menstrual disorders, including infrequent or frequent menstruation, prolonged or shortened menstrual periods, amenorrhea, and irregular menstrual flow. (3)?Biochemical confirmation with anti-Müllerian hormone (AMH) 10 IU/L for two consecutive menstrual cycles.?; (4)?Subjects must fully understand the purpose, procedures, and related requirements of this study, and voluntarily sign an informed consent form to indicate their willingness to participate in the study.??

Exclusion criteria

Exclusion criteria: (1) Pregnant and lactating subjects; (2) Individuals with congenital developmental abnormalities of the reproductive organs, or primary or secondary amenorrhea caused by acquired organic diseases or injuries to the reproductive organs; (3) Individuals who are allergic to multiple drugs or known to be allergic to the components of the study product.?; (4) Have not received relevant treatment, such as the administration of estrogen and progesterone, traditional Chinese medicine, etc., within the past 3 months; (5) Patients with severe cardiovascular, cerebrovascular, or hepatic and renal dysfunction, as well as mental illness; (6) Individuals with a history of or concurrent malignant tumors; (7) Patients deemed unsuitable for participation in the study by the researcher.??

Design outcomes

Primary

MeasureTime frame
The improvement of the menstrual cycle;The degree of improvement in menopausal symptom;The improvement of quality of life;

Secondary

MeasureTime frame
serum anti-Müllerian hormone (AMH);Follicle-Stimulating Hormone (FSH);Estradiol (E2);Luteinizing Hormone (LH);B-ultrasound examination of Antral Follicle Count (AFC);

Countries

China

Contacts

Public ContactZhou Jinhong

?Zhejiang Hospital??

zhoujh2440@126.com+86 571 8798 7373

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026