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Evaluation of therapeutic effect of acupoint catgut embedding therapy on POI with yin deficiency of liver and kidney based on the theory of "deep acceptance but long stay"

Evaluation of therapeutic effect of acupoint catgut embedding therapy on POI with yin deficiency of liver and kidney based on the theory of "deep acceptance but long stay"

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082026
Enrollment
Unknown
Registered
2024-03-19
Start date
2020-09-08
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

premature ovarian insufficiency ,POI

Interventions

Control group:Artificial cycle therapy: Estradiol valerate tablets (Guangzhou Branch of Bayer Healthcare Co., Ltd. National Medicine Standard: J20080036) 1mg/ day, taken continuously for 21 days. On t
if you don't have menstrual cramps, start the next medication cycle one week after stopping taking medicine.
Experimental group:Acupoint catgut embedding in the experimental group mainly refers to the selection criteria of amenorrhea and menoxenia in Acupuncture, a textbook of the 12th Five-Year Plan of the

Sponsors

Dongzhimen Hospital Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: ? Non-pregnant women of childbearing age aged 18-40; ? Sporadic menstruation or amenorrhea for at least 4 months; ? Serum basal FSH > 25U/L at least twice (interval > 4 weeks); ? Accompanied by at least three of the following symptoms: soreness of waist and knees, hot flashes, sweating, tinnitus, poor sleep, dry eyes, vaginal dryness, dizziness, dry skin, irritability, etc. ? Those who have not taken any hormones or drugs that affect endocrine hormones in recent 3 months; ? Informed and voluntarily participated in this clinical trial, and signed the informed consent form of clinical trial.

Exclusion criteria

Exclusion criteria: (1) Ovarian dysfunction caused by organic genital lesions; (2) those with or with other endocrine diseases; (3) allergic characteristics and allergic to experimental drugs; (4) Those who do not meet the case inclusion criteria or fail to use drugs according to regulations and have poor compliance; (5) Patients with serious primary diseases and mental disorders such as heart, liver, brain, kidney and hematopoietic system; (6) Pregnant and lactating women and those who have never had sex.

Design outcomes

Primary

MeasureTime frame
Follicle Stimulating Hormone,FSH;

Secondary

MeasureTime frame
Estradiol,E2;Luteinizing Hormone,LH;Peak Systolic Velocity, PSV;End - Diastolic Velocity,EDV;Antral Follicle Coun,AFC;ovarian volume;ovarian arterial resistance index,RI;ovarian blood flow pulsation index,PI;integrals of TCM syndromes;improved Kupperman score;

Countries

China

Contacts

Public ContactNi Jinxia

Dongzhimen Hospital Beijing University of Chinese Medicine

nijinxia118@126.com+86 10 8401 3161

Outcome results

None listed

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