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Observation on the Efficacy of Modified Erxian Decoction in Treating Patients with Kidney Deficiency and Blood Stasis Type Menstrual Reduction

Observation on the Efficacy of Modified Erxian Decoction in Treating Patients with Kidney Deficiency and Blood Stasis Type Menstrual Reduction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000519
Enrollment
Unknown
Registered
2026-03-13
Start date
2025-04-09
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

Hypomenorrhea

Interventions

observation group:Er Xian Zelan Decoction
control group:Estradiol tablets/estradiol and progesterone tablets (2-10mg)

Sponsors

Wangjing Hospital of China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: (1) Meets the Traditional Chinese Medicine (TCM) criteria for 'scanty menstruation' and the differentiation of 'kidney deficiency with blood stasis,' and meets the Western medicine diagnostic criteria for ovulatory scanty menstruation; (2) Women aged 20–40 years; (3) Experiencing scanty menstruation for three or more menstrual cycles; (4) Patients voluntarily agree to participate in this study and have signed the relevant informed consent form.

Exclusion criteria

Exclusion criteria: (1) Individuals with congenital uterine malformations or hypoplastic uterus; (2) Endometrial tuberculosis patients; (3) Individuals with severe malnutrition caused by chronic conditions such as malnutrition, malignant tumors, or other wasting diseases; (4) Patients with organic lesions such as intrauterine adhesions and massive ovarian masses; (5) Those who have used medications affecting menstruation within the past 3 months; (6) Individuals allergic to any component of the prescription medication; (7) Patients with severe primary diseases such as cardiovascular, hepatic, renal, and hematopoietic system disorders, as well as psychiatric patients; (8) Breastfeeding women or those who refuse to use contraception during the study period; (9) Individuals with intrauterine devices such as Mirena or other similar contraceptive devices; (10) Patients with active venous or arterial thromboembolic diseases within the past 6 months.

Design outcomes

Primary

MeasureTime frame
menstrual flow; Traditional Chinese Medicine Syndrome Score;

Secondary

MeasureTime frame
Endometrial thickness;Uterine pulsatility index;Uterine resistance index;End Systolic Peak/End Diastolic Peak;Follicle-stimulating Hormone;luteinizing hormone;estradiol;testosterone;Anti Mullerian hormone;

Countries

China

Contacts

Public ContactDING Yongfen

Wangjing Hospital of China Academy of Chinese Medical Sciences

dyfdr1998@126.com19537593040

Outcome results

None listed

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