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Clinical effect of Bushen Anshen Decoction Combined with Wuyin therapy on perimenopausal female insomnia patients with kidney deficiency and liver depression

Clinical effect of Bushen Anshen Decoction Combined with Wuyin therapy on perimenopausal female insomnia patients with kidney deficiency and liver depression

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2024000873
Enrollment
Unknown
Registered
2024-12-27
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Perimenopausal insomnia

Interventions

Western medicine group:Dexzopiclone + oryzanol
Wuyin treatment group:Dexzopiclone + oryzanol+Wuyin therapy
Bushen Anshen Decoction group:Dexzopiclone + oryzanol+Bushen Anshen Decoction
Combined treatment group:Dexzopiclone + oryzanol+Bushen Anshen Decoction+Wuyin therapy

Sponsors

Chen Pei
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
45 Years to 55 Years

Inclusion criteria

Inclusion criteria: (1) Aged between 45 and 55 years old in the perimenopausal period; (2) Western medicine diagnosis: according to the international classification of sleep disorders it meets the relevant standards of insomnia (such as difficulty in falling asleep difficulty in maintaining sleep early awakening etc.); (3) The dialectical classification is kidney deficiency and liver depression; (4) No history of major diseases (such as serious heart disease liver and kidney dysfunction etc.) affecting treatment or sleep; (5) Voluntary participation in the study participants need to have treatment compliance voluntarily participate in the study and comply with the study protocol including regular follow-up and receiving treatment intervention; (6) And signed the informed consent.

Exclusion criteria

Exclusion criteria: (1) There are serious organic diseases (such as cardiovascular disease liver and kidney dysfunction etc.); (2) Have a history of mental illness or are receiving psychotherapy; (3) Previous ovariectomy hysterectomy or surgical treatment of uterus ovary and breast; (4) Pregnant or lactating women; (5) Taking other drugs that affect sleep such as sleeping pills.

Design outcomes

Primary

MeasureTime frame
PSQI;

Secondary

MeasureTime frame
SF-36;neurotransmitter;HAMA;sex hormone;HAMD;

Countries

China

Contacts

Public ContactChen Pei

Xi'an Fifth Hospital

chenpeii@qq.com18408257161

Outcome results

None listed

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