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Clinical effect evaluation of transcutaneous electrical acupoint stimulation on patients with stable COPD

Clinical effect evaluation of transcutaneous electrical acupoint stimulation on patients with stable COPD

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14004500
Enrollment
Unknown
Registered
2014-04-10
Start date
2014-04-14
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 obstructive pulmonary disease

Interventions

Sponsors

Integrative Medicine department, West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Comply with the diagnosis of "lung distention" syndrome of TCM; (2) Comply with the Western medicine diagnosise of "stable chronic obstructive pulmonary disease"; (3) Aged 40 to 75 years; (4) With clear consciousness, being able to walk independently; (5) Sign the informed consent form; (6) Had no previous experience of TEAS.

Exclusion criteria

Exclusion criteria: 1. Patients with severe heart, brain, blood vessels, liver and kidney dysfunction, cancer patients,and severe mental disorders; 2. pregnant and lactating women; 3. Have an acute exacerbation of COPD in three months; 4. have attended any other studies in six months; 5. obvious lesions in bones and muscles may affect 6MWT; 6. allergic to the sticking agent.

Design outcomes

Primary

MeasureTime frame
Lung function;6 Minute Walk Test;Dyspnea Visual Analogue Scale;COPD Assessment Test;Oxygen saturation;

Countries

China

Contacts

Public ContactMao Bing

West China Hospital, Sichuan University

maobing@medmail.com.cn+86 18980601724

Outcome results

None listed

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