Study on Acupuncture Treatment of Chronic Airway Diseases(Asthma and Chronic Obstructive Pulmonary Disease)

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-80
SponsorHenan University of Traditional Chinese Medicine

About this trial

For patients in the acute phase of chronic airway diseases, on the basis of guideline-directed treatment, the experimental group was given acupuncture treatment, while the control group was given sham acupuncture treatment. The treatment lasted for one week, followed by a 13-week follow-up. For asthma and COPD, PEF and CAT were respectively used as the primary outcome measures to evaluate the clinical efficacy and safety of acupuncture. Based on the improvement of the primary outcome measures, the advantageous population was identified. The mechanism by which acupuncture reduces airway mucus hypersecretion was preliminarily explained.

Eligibility criteria

Qualifiers

Meets the diagnostic criteria for acute attack of asthma/AECOPD;

Age range from18 years to 80 years(asthma) and 40 yesrs to 80 years(COPD);

The investigators agreed to participate in this clinical study by voluntarily signing an informed consent form.

Disqualifiers

Patients with combined pulmonary abscess, pulmonary interstitial fibrosis, active pulmonary tuberculosis, bronchiectasis and other pulmonary diseases;

Patients with severe cardiovascular and cerebrovascular diseases (such as malignant arrhythmia, unstable angina pectoris, acute myocardial infarction, grade 3 or above cardiac function, stroke, cerebral hemorrhage, etc.);

Patients with severe liver diseases (such as liver cirrhosis, portal hypertension and bleeding caused by esophageal and gastric fundus varices) and severe kidney diseases (such as dialysis, kidney transplantation, etc.);

Patients with impaired consciousness or various mental disorders who are unable to communicate normally;

Trial design

Treatments tested in this trial

  • Acupuncture
  • Sham Acupuncture

Treatment groups

576 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

Henan University of Traditional Chinese Medicine

Lead sponsor

First Teaching Hospital of Tianjin University of Traditional Chinese Medicine

Collaborator

Hebei Provincial Hospital of Traditional Chinese Medicine

Collaborator