Skip to content

The Clinical Study of Erzhi pill Assisting on Treatment of Menopausal Hypertension

A Randomized, Double-Blind, Placebo-Controlled Trial of Erzhi pill Assisting on Treatment of Menopausal Hypertension

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-17012999
Enrollment
Unknown
Registered
2017-10-16
Start date
2017-10-09
Completion date
Unknown
Last updated
2017-10-23

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

Conditions

Menopausal Hypertension

Interventions

group A:hypotensor+erzhi pill
group B:hypotensor+placebo

Sponsors

Second Affiliated Hospital of Tianjin University of TCM
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. femal aged 45 to 65years old, during the period of perimenopause or early postmenopause (less than 5years); 2. patients with hypertension grade 1 or 2; 3. diagnosed hypertension during menopause; 4. liver and kindey yin-deficiency; 5. informed consent form has been signed.

Exclusion criteria

Exclusion criteria: 1. secondary hypertension; 2. Known hypersensitivity to the investigational drugs or their ingredients; 3. Patients with diseases as follows:malignant tumor; hyperthyroidism,hypothyroidism, uncontrolled diabetes; obesity (body mass index greater than 30); neurasthenia, psychiatric disorders, migraine headache;hematopoietic system diseaseautoimmune system diseases; Fungal or bacterial vaginal infections; 4. Surgical menopause; 5. Abnormal liver function or abnormal renal function; 6. The participants used the same treatment of traditional Chinese medicine in the previous 4 weeks. Use Estrogen or estrogen/progesterone drugs through vaginal or percutaneous or oral style in the previous 8 weeks. Take progesterone implants and a separate injection of estrogen therapy in the previous 3 months, Take estrogen pills or progesterone injection in the previous 6 months.

Design outcomes

Primary

MeasureTime frame
24hour ambulatory blood pressure;Menopause-specific quality-of-life (MENQOL);

Secondary

MeasureTime frame
FSH, E2, Testosterone;Serum lipids (total cholesterol, HDL and LDL chole;count numbers (EPCs, CECs);

Countries

China

Contacts

Public ContactGao Xiumei

Tianjin University of Traditional Chinese Medicine (TCM)

gaoxiumei@tjutcm.edu.cn+86 13602020716

Outcome results

None listed

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