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NCT07131020Recruiting

Study on the Mechanism of Yifei Moxibustion Improving Immune Function in COPD Based on Plasma Exosome miRNAs

Study on the Mechanism of Yifei Moxibustion in Enhancing Immune Function in Chronic Obstructive Pulmonary Disease Based on Plasma Exosomal miRNAs

Source: ClinicalTrials.gov · Last updated 19 Aug 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This study adopted a randomized controlled design, enrolling 90 patients and 30 healthy volunteers. The patients were randomly divided into the Yifei Moxibustion group, the conventional Western medicine treatment group, and the TCM syndrome differentiation treatment group, and were treated for 3 months. Peripheral venous blood was collected from both the healthy volunteers and the patients to observe indicators such as T cell subsets and immunoglobulins, to evaluate the effect of Yifei Moxibustion on improving immune function. The regulation of target genes by exosomes and potential action targets and molecular mechanisms were preliminarily verified through techniques such as nanoparticle tracking technology and flow cytometry.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
120 (estimated)
First submitted
10 Aug 2025
Start date
11 May 2024
Primary completion date
Sept 2025
Lead sponsor
Henan University of Traditional Chinese Medicine
Diseases
COPD
NCT number
NCT07131020

What you commit to

  • Study type: Interventional
  • Planned participants: 120
  • From 11 May 2024 to the primary completion date, Sept 2025
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Pregnant and lactating women;
    • Patients with cognitive impairment, confusion, dementia, or various mental disorders;
    • Patients with unstable angina pectoris or acute myocardial infarction;
    • Patients with a history of syncope after exercise or bone and joint diseases that affect exercise; ⑤ Patients with pneumothorax, pleural effusion, pulmonary embolism, or tumors;
    • Patients known to be allergic to the ingredients of the moxibustion powder.

Who the study is looking for

  • Patients who meet the diagnostic criteria for stable chronic obstructive pulmonary disease;
    • Patients who meet the TCM diagnostic criteria for lung qi deficiency, lung-spleen qi deficiency, and lung-kidney qi deficiency; ③ Aged 18 to 80 years old; ④ Voluntarily signed the informed consent form.

Age in the registry: 18 years to 80 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
The First Affiliated Hospital of Henan University of Chinese Medicine
Coordinator of this site? Confirm its status
ZhengzhouChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.