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Clinical Efficacy Study of Deer Placenta Extract in Treating Scanty Menstruation Due to Qi and Blood Deficiency

Clinical Efficacy Study of Deer Placenta Extract in Treating Scanty Menstruation Due to Qi and Blood Deficiency

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000432
Enrollment
Unknown
Registered
2026-02-26
Start date
2021-10-01
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Light menstrual flow

Interventions

Traditional Chinese Medicine Group:Oral Deer Placenta Extract
Western Medicine Group:Take Femotone
Joint Group:Take Fenmatong and deer placenta ointment orally at the same time.

Sponsors

Beijing Obstetrics and Gynecology Hospital Affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: (1) Meets diagnostic criteria for hypomenorrhea with Traditional Chinese Medicine pattern identification of qi and blood deficiency; (2) Age 18–40 years; (3) Absence of severe cardiovascular or cerebrovascular diseases; (4) Signed informed consent form; (5) Able to maintain stable follow-up.

Exclusion criteria

Exclusion criteria: (1) Individuals who do not meet Western medical diagnostic criteria or Traditional Chinese Medicine (TCM) pattern differentiation standards; (2) Patients with concomitant primary diseases such as liver/kidney disorders, cardiovascular/cerebrovascular conditions, hematological disorders, diabetes, or psychiatric illnesses; (3) Patients with malignant tumors including endometrial cancer, ovarian cancer, or breast cancer; (4) Patients with allergic constitutions, such as those with a history of allergy to two or more drugs or foods; or those with known allergy to any component of this drug; (5) Patients unable to comply with treatment or attend follow-up visits; (6) Patients currently participating in other drug clinical trials; (7) Pregnant or lactating women; (8) Patients concurrently taking other medications for hypomenorrhea.

Design outcomes

Primary

MeasureTime frame
Menstrual bleeding chart;

Secondary

MeasureTime frame
Follicle stimulating hormone(FSH);Luteinizing hormone(LH);Follicle stimulating hormone(FSH)/Luteinizing hormone(LH);Anti-M ü llerian hormone;Antral follicle count;

Countries

China

Contacts

Public ContactXin Mingwei

Beijing Obstetrics and Gynecology Hospital Affiliated to Capital Medical University

13552866767@163.com13552866767

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Apr 4, 2026