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Changes of Functional Connectivity, Reho and ALFF after acupunctured Zusanli point tested by Resting-state functional magnetic resonance imaging

Changes of Functional Connectivity, Reho and ALFF after acupunctured Zusanli point tested by Resting-state functional magnetic resonance imaging

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TCC-09000516
Enrollment
Unknown
Registered
2009-08-27
Start date
2008-10-01
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

Chronic Gastritis and Stroke

Interventions

normal group:acupunctureat Zusanli point
Stroke group:acupunctureat Zusanli point
Chronic gastritis group:acupunctureat Zusanli point

Sponsors

Guangdong Provincial Hospital of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 65 Years

Inclusion criteria

Inclusion criteria: Normal group: 1. Healthy; No case history of psychoneural system; No physical and mental symptom in the near future of experiment, such as pain or depression and so on; 2. Between the age from 30 to 65 years old; 3. Right handedness; 4. The subjects who have already signed the informed consent. Chronic gastritis group: 1. Healthy; No case history of psychoneural system; No physical and mental symptom in the near future of experiment,such as pain or depression and so on; 2. Between the age from 30 to 65 years old; 3. Right handedness; 4. Gastric tumor was exclude by gastroscope; 5. The patient with typical functional stomach illness symptom; 6. The subjects who have already signed the informed consent. Stroke group: 1. Healthy; No case history of psychoneural system; No physical and mental symptom in the near future of experiment, such as pain or depression and so on; 2. Aged from 30 to 65 years old; 3. Right handedness; 4. The patient more than 3 months after first stroke; 5. The subjects who have already signed the informed consent.

Exclusion criteria

Exclusion criteria: 1. No serious visual disorder and hearing disturbance; 2. History of metal in the body or operation; 3. The women who were in the process of menses or pregnancy; 4. History of serious primary diseases of hepatic, renal, hematopoietic and endocrine system, or psychosis, diabetes mellitus, or having taken excessive alcohol or abused medicines; or malignant tumor; 5. History of having taken sedative within one week before experiment.

Design outcomes

Primary

MeasureTime frame
Regional homogeneity;Functional Connectivity;Amplitude of low-frequency fluctuation;

Countries

China

Contacts

Public ContactYu Long
jackyulong@163.com+86 020 81887233-38112

Outcome results

None listed

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