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NCT07058259Active, not recruiting

Acupuncture for Persistent Dyspnea Despite Medical Treatment in COPD

The Effect of Acupuncture in COPD Patients With Persistent Dyspnea Despite Medical Treatment

Source: ClinicalTrials.gov · Last updated 10 Jul 2025

Brief summary (registry, in English)

This randomized controlled trial aims to evaluate the effectiveness of acupuncture as an adjunctive non-pharmacological therapy in patients with stable COPD who continue to experience dyspnea despite optimal medical treatment.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
60 (estimated)
First submitted
22 Jun 2025
Start date
15 Nov 2024
Primary completion date
30 Jun 2025
Lead sponsor
Istanbul Medeniyet University
Diseases
COPD
NCT number
NCT07058259

What you commit to

  • Study type: Interventional
  • Planned participants: 60
  • From 15 Nov 2024 to the primary completion date, 30 Jun 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.

Prior treatment

  • COPD patients receiving monotherapy,
  • Patients receiving long-term oxygen therapy (LTOT),

Other illness

  • Patients currently experiencing a COPD exacerbation or with a history of exacerbation within the past month,
  • Patients with unstable angina, acute myocardial infarction (within 3-5 days), uncontrolled arrhythmia, active endocarditis, acute myocarditis/pericarditis, symptomatic severe aortic stenosis, lower extremity DVT, uncontrolled asthma/COPD, pulmonary edema, oxygen saturation (SpO₂) ≤ 90%, acute respiratory failure, or suspected dissecting aneurysm,

Other

  • Patients who do not consent to participate in the study,
  • Patients with communication difficulties or with visual, walking, or hearing impairments,
  • Patients with Stage 1 COPD (FEV1 ≥ 80%),
  • Patients with mMRC score \<2 and CAT score \<10,
  • COPD patients who have experienced more than two exacerbations in the past year.
    • Withdrawal Criteria:
  • Patients who are unable to complete acupuncture sessions or follow-up assessments in the control group for any reason,
  • Patients who experience an exacerbation during the study (they will be reassessed one month after recovery and may be re-included if eligible),
  • Patients who miss more than two acupuncture sessions.

Who the study is looking for

  • Volunteers aged between 40 and 80 years, who are communicative and cooperative,
  • Diagnosed with COPD for at least 3 months,
  • Receiving dual or triple regular pharmacological therapy for at least 3 months,
  • Post-bronchodilator FEV1/FVC \<70% and predicted FEV1 \<80% on spirometry, mMRC (Modified Medical Research Council) dyspnea score of 2 or higher,
  • COPD Assessment Test (CAT) score of 10 or higher.

Age in the registry: 40 years to 80 years · Sex: All · Does not accept 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
Istanbul Medeniyet University Faculty of Medicine
Coordinator of this site? Confirm its status
IstanbulTurkey (Türkiye)Unknown status

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