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The treatment of thin endometrial related infertility (spleen and kidney Yang deficiency)

The treatment of thin endometrial related infertility (spleen and kidney Yang deficiency)

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400084571
Enrollment
Unknown
Registered
2024-05-20
Start date
2024-05-28
Completion date
Unknown
Last updated
2024-05-27

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

Conditions

Thin endometrium-related infertility (deficiency of spleen and kidney Yang)

Interventions

test team:Menstrual regulation and pregnancy promotion pill, oral, 5g (50 pills), twice a day. Take it for 20 consecutive days from the 5th day of the menstrual cycle for 3 consecutive menstrual cycle
control group:Estradiol valerate tablets: Patients with regular menstruation began to take estradiol valerate tablets on the 9th day of menstruation, 2mg/ day, and have been taking until 2 weeks after

Sponsors

Peking University Third Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. According to the diagnosis of thin endometrium; 2. TCM syndrome differentiation of deficiency of spleen and kidney Yang; 3. There are currently pregnant with needs and planners; 4. 20-40 years old (inclusive); 5. Menstrual cycle of 21-35 days, 3 consecutive natural cycles of ovulation, and the sex hormone levels are normal; 6. At least one side of the fallopian tube patency; 7. The informed consent process is fully compliant.

Exclusion criteria

Exclusion criteria: 1. Patients with myometrial lesions (such as severe adenomyosis with uterine cavity deformation, etc.), endometrial tuberculosis, and uterine embolism; 2. Patients with severe intrauterine adhesion; 3. Infertility caused by bilateral fallopian tube obstruction, uterine fibroids, endometrial polyps, immune factors, endometriosis or congenital dysplasia and malformation of the reproductive system; 4. Patients with polycystic ovary syndrome, premature ovarian failure, hyperprolactinemia, hypothyroidism and other metabolic diseases or other abnormal endocrine function that affect ovulation function; 5. Patients with severe hyperplasia of breast nodules; 6. Infertility caused by the abnormal reproductive function of the man; 7. Contraindications to the use of estrogen therapy (such as patients with active venous or arterial thromboembolic disease, breast cancer, known or suspected estrogen-dependent tumors, severe liver and kidney dysfunction, blood porphyria, otosclerosis, systemic lupus erythematosus, etc.); 8. Contraindications to the use of progesterone therapy (such as liver and kidney insufficiency, cardiovascular disease, hypertension, diabetes, epilepsy, undiagnosed vaginal bleeding, patients with a history of thrombosis and gallbladder disease, etc.); 9. People with severe cardiovascular and cerebrovascular diseases, liver, kidney and other diseases, mental illness and severe neurosis; 10. Persons allergic to known ingredients in the trial drug; 11. The investigator does not consider it appropriate to attend the investigator.

Design outcomes

Primary

MeasureTime frame
Endometrial thickness on ovulation day of the 3rd menstrual cycle;

Secondary

MeasureTime frame
Endometrial thickness at different time points during the observation period;Cycle pregnancy rate;Endometrial blood flow index at different ovulation days during the observation period;Changes of endometrial morphology and composition in different ovulation days during the observation period;The change value and effective rate of TCM syndromes at different time points during the observation period;The disappearance rate of single symptom of TCM at different time points during the observation period;

Countries

China

Contacts

Public ContactRong Ling

Peking University Third Hospital

roseli001@sina.com+86 137 0108 5402

Outcome results

None listed

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