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Clinical observation of the addition and subtraction of Erxian decoction and Liuwei Dihuang pills combined with electroacupuncture in the treatment of perimenopausal insomnia (yin and yang deficiency type).

Clinical observation of the addition and subtraction of Erxian decoction and Liuwei Dihuang pills combined with electroacupuncture in the treatment of perimenopausal insomnia (yin and yang deficiency type).

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400081708
Enrollment
Unknown
Registered
2024-03-10
Start date
2024-03-10
Completion date
Unknown
Last updated
2024-03-11

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

Conditions

Perimenopausal insomnia

Interventions

Experimental group:Erxian Decoction and Liuwei Dihuang Pill combined with electroacupuncture
Control group:Oral alprazolam

Sponsors

the affilinated Acunpuncture and Tuina hospital of Shanxi University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 55 Years

Inclusion criteria

Inclusion criteria: (1) Meet the above diagnostic criteria; (2) The total score of PSQI = 7 points; (3) Modified Kupperman score= 15 points; (4) Able to understand the content of the observation table and cooperate with the researcher; (5) Those who signed the informed consent form and voluntarily participated in this study.

Exclusion criteria

Exclusion criteria: (1) Insomnia caused by other reasons; (2) Have taken any insomnia-related drugs in the past 1 month; (3) Patients with ovarian disease or bilateral oophorectomy; (4) Vaginal bleeding of unknown cause; (5) Those who are participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
PSQI;

Secondary

MeasureTime frame
TCM Syndrome Scoring Scale;KMI;Sex hormone levels;

Countries

China

Contacts

Public ContactHaijun Wang

the affilinated Acunpuncture and Tuina hospital of Shanxi University of Chinese Medicine

whjdavid@163.com+86 158 0340 9395

Outcome results

None listed

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