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A Clinical Research on Treating Insomnia of Fire Derived from Stagnation of Liver-Qi Type by Blood-Letting Puncture and Cupping Therapy

A Research on Effect of Blood-Letting Puncture and Cupping Therapy to Insomnia of Fire Derived from Stagnation of Liver-Qi Type in Functional Brain Imaging

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-ICR-15006021
Enrollment
Unknown
Registered
2015-02-22
Start date
2015-04-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Insomnia

Interventions

Experimental group:Pricking blood adding cupping
Control Group :Oral Estazolam
Blank Group :Untreated

Sponsors

Teaching Hospital of Chengdu University of T.C.M
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Has typical symptom of insomnia, accords with insomnia diagnosis standard in chinese and western medicine andaccords with insomnia of fire derived from stagnation of liver-Qi type; 2. The figure of PSQI is greater than or equal to 7; 3. The course is more than a month; 4. Right-handed(in daily life), age is between 18-65 years, male or female; 5. Has signed the informed consents. The selectees must meet all criteria above.

Exclusion criteria

Exclusion criteria: 1. Insomnia caused by systemic disease such as ache, fever, cough,operation, etc, and disturbance from circumstancesof the outside; 2. Non right-handed, age is under 18s or over 65s, women during pregnant stage and breast-feed stage; 3. Has primary disease belong to cardiovascular system, lung, liver, kidney, hematopoietic system, etc, and psychotic, coagulopathy exist; 4. ebrietas, astheno-bulbospinal paralysis, and someone easily suffer angle-closure glaucoma; 5. The metal subject has been implanted in the body, or other contraindications of fMRI examination; patient meet any criterion above must be ruled out.

Design outcomes

Primary

MeasureTime frame
PSQI;TCM Syndrom Scale;Self-Rating Anxiety Scale(SAS);Self-Rating Depression Scale (SDS);

Countries

China

Contacts

Public ContactFeng Fen
790334253@qq.com+86 13547959969

Outcome results

None listed

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