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NCT06948578Completed

Thread-Embedding Acupuncture for Functional and QoL Improvement in COPD Patients

Effectiveness and Safety of Thread-Embedding Acupuncture in Improving Functional Capacity and Quality of Life in Patients With Chronic Obstructive Pulmonary Disease

Source: ClinicalTrials.gov · Last updated 29 Dec 2025

Brief summary (registry, in English)

The goal of this clinical trial is to learn if thread-embedding acupuncture (TEA) can improve functional capacity and quality of life of chronic pulmonary disease (COPD) patients. The main questions it aims to answer are: * Does TEA, when combined with standard treatment, improve functional capacity measured by the six-minute walking test (6MWT) and the modified Medical Research Council (mMRC) scale at 1, 2, and 3 months after the intervention? * Does TEA, when combined with standard treatment, improve quality of life as measured by the COPD Assessment Test (CAT) and the St. George's Respiratory Questionnaire (SGRQ) at 1, 2, and 3 months after intervention? Researchers will compare TEA to sham TEA (a placebo procedure without thread implantation) to determine if TEA leads to meaningful improvements in COPD patients. Participants will: * Complete assessment using 6MWT, mMRC, CAT, and SGRQ * Receive one session of either TEA or sham TEA * Return to the clinic once a month for follow-up assessments over a 3-month period

Status (registry)
Completed
Study type
Interventional
Enrollment
34 (actual)
First submitted
22 Apr 2025
Start date
1 Jul 2025
Primary completion date
30 Nov 2025
Lead sponsor
Universitas Indonesia
Diseases
COPD
NCT number
NCT06948578

What you commit to

  • Study type: Interventional
  • Participants enrolled: 34
  • From 1 Jul 2025 to the primary completion date, 30 Nov 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

  • Undergoing acupuncture therapy within the last 2 weeks or thread-embedding acupuncture (TEA) within the last 6 months.

Other illness

  • Presence of tumors, wounds, inflammation, or skin infection at the needling area.
  • Uncontrolled heart disease or diabetes.
  • History of malignancy, uncontrolled epilepsy, or psychiatric disorders.
  • Known allergy to stainless steel or polydioxanone (PDO) thread.

Lab values

  • Blood disorders or use of blood-thinning medications (antiplatelets or anticoagulants) with INR \> 2.0.
  • Capillary blood glucose level ≥200 mg/dL (measured using glucometer).

Other

  • Pregnant women.

Who the study is looking for

  • Male or female participants aged 18 to 70 years.
  • Body Mass Index (BMI) ≥18.5 kg/m².
  • Diagnosed with stable chronic obstructive pulmonary disease (COPD) based on GOLD criteria.
  • Willing to participate in the study until completion and has signed informed consent.

Age in the registry: 18 years to 70 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
Universitas Indonesia
Coordinator of this site? Confirm its status
Jakarta PusatIndonesiaUnknown status

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