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Clinical Assessment of Acupuncture for the Treatment of Chronic Asthma

Primary Purpose

Asthma

Status
Completed
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Verum acupuncture
Sham acupuncture
Sponsored by
Shanghai University of Traditional Chinese Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Asthma focused on measuring Efficacy, Acupuncture, Asthma

Eligibility Criteria

14 Years - 65 Years (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients diagnosed with mild-to-moderate persistent asthma
  • Forced expiratory volume in one second (FEV1) reversibility of greater than or equal to 12% following bronchodilator administration (2 puffs)
  • Patients who have given written informed consent

Exclusion Criteria:

  • Participation in another clinical trial 1 month prior to study entry
  • Use of systemic corticosteroids 2 weeks prior to study entry
  • Patients with general infection, lower respiratory infection, pulmonary tuberculosis and fungal infection 1 month prior to study entry
  • Hospitalization due to acute exacerbation 3 months prior to study entry
  • Patients cannot stop using forbidden drugs which include inhaled corticosteroid, theophylline, long-term β2 agonist, sodium cromoglicate, leukotrienes antagonist and anticholinergic drug
  • Patients who are allergic to albuterol and corticosteroid
  • Patients with severe primary diseases such as cancer, cardiovascular system, liver, kidney and hematopoietic system diseases
  • Wheeze caused by pulmonary tuberculosis, bronchiectasia and cardiac insufficiency
  • Patients with hyperthyroidism
  • Patients with mental illness, acrasia
  • Female patients in pregnancy, lactation period and planning to get pregnant during the trial
  • Any significant disorder that in the investigator's opinion, might put the patients at risk or influence the study outcomes
  • Acupuncture contraindications: serious allergic or infectious dermatitis and hemorrhagic diseases such as thrombocytopenic purpura and hemophilia

Sites / Locations

  • University Hospital of Gansu Traditional Chinese Medicine
  • Kaifeng Traditional Chinese Medicine hospital
  • No.3 hospital of Henan college of Traditional Chinese Medicine
  • Zhengzhou Traditional Chinese Medicine hospital
  • Xiangya Hospital of Central South University
  • Shanghai First People's Hospital
  • Shanghai research institute of acupuncture and meridian,Yueyang Hospital of Integrated Traditional Chinese and Western Medicine
  • Shanghai Dachang hospital
  • Longhua Hospital
  • Shanghai TCM Integrated hospital
  • Shuguang Hospital
  • Wenzhou Hospital of Traditional Chinese Medicine

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Verum acupuncture

Sham acupuncture

Arm Description

Verum acupuncture treatment once every two days + Albuterol sulfate HFA (Ventolin®™ 100 mcg Inhalation Aerosol) as needed + Prednisone Acetate Tablets(H31020675, 5 mg oral tablet) for exacerbation

Sham acupuncture treatment once every two days + Albuterol sulfate HFA (Ventolin®™ 100 mcg Inhalation Aerosol) as needed + Prednisone Acetate Tablets(H31020675, 5 mg oral tablet) for exacerbation

Outcomes

Primary Outcome Measures

Total score Change from Baseline of Asthma Control Test

Secondary Outcome Measures

Percentage of symptom-free days
Usage of salbutamol and prednisone
Lung function(FEV1, PVC, FEV1/FVC%, FEV1/predicted%),morning/evening PEF
Asthma symptom scores
Asthma quality of Life Questionnaire(AQLQ)
Total number of exacerbations that require systemic corticosteroid therapy
Eosinophil (EOS) count in peripheral blood, T cell classification, serum cytokine levels

Full Information

First Posted
August 26, 2013
Last Updated
April 14, 2016
Sponsor
Shanghai University of Traditional Chinese Medicine
Collaborators
Shanghai Municipal Health Bureau, National Natural Science Foundation of China
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1. Study Identification

Unique Protocol Identification Number
NCT01931696
Brief Title
Clinical Assessment of Acupuncture for the Treatment of Chronic Asthma
Official Title
Clinical Assessment of Acupuncture for the Treatment of Asthma: A Randomized, Multicenter, Double-blind, Parallel-group Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
July 2013 (undefined)
Primary Completion Date
February 2015 (Actual)
Study Completion Date
July 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shanghai University of Traditional Chinese Medicine
Collaborators
Shanghai Municipal Health Bureau, National Natural Science Foundation of China

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to assess whether acupuncture is effective in the treatment of chronic asthma.
Detailed Description
Asthma is a common chronic disease worldwide with an estimated 300 million affected individuals. In analyses of economic burden of asthma, apart from direct medical costs including hospital admissions and cost of medications, indirect, non-medical costs such as time lost from work account for a considerable part. For all but the most severe patients, the ultimate goal is to prevent symptoms, minimize morbidity from acute episodes, and prevent functional and psychological morbidity to provide a near healthy lifestyle. Although the symptoms can be controlled by drug treatment in most patients, effective low-risk, non-drug approaches such as acupuncture could constitute a significant advance in asthma management. The purpose of this study is to assess whether acupuncture is effective in the treatment of chronic asthma. There is a 1-week screening period(-1 week) during which participants will be monitored while they use an albuterol inhaler as needed. Study visits will occur at weeks 0(Baseline), weeks 3, weeks 6. Participants will undergo a physical examination, lung function, blood and urine collection. At the Weeks 0 study visit, participants will be randomly assigned to one of the following two groups for 6 weeks of treatment: Group 1 will receive verum acupuncture treatment once every two days plus albuterol as needed, prednisone for exacerbation Group 2 will receive sham acupuncture treatment once every two days plus albuterol as needed, prednisone for exacerbation Study visits will occur at Weeks 0, 3, 6. A physical examination, blood collection, and lung function will occur at selected visits. Questionnaires to assess asthma control and quality of life will also be completed. Throughout the study, participants will record asthma symptoms and medication usage in a daily diary.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
Efficacy, Acupuncture, Asthma

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Verum acupuncture
Arm Type
Experimental
Arm Description
Verum acupuncture treatment once every two days + Albuterol sulfate HFA (Ventolin®™ 100 mcg Inhalation Aerosol) as needed + Prednisone Acetate Tablets(H31020675, 5 mg oral tablet) for exacerbation
Arm Title
Sham acupuncture
Arm Type
Sham Comparator
Arm Description
Sham acupuncture treatment once every two days + Albuterol sulfate HFA (Ventolin®™ 100 mcg Inhalation Aerosol) as needed + Prednisone Acetate Tablets(H31020675, 5 mg oral tablet) for exacerbation
Intervention Type
Device
Intervention Name(s)
Verum acupuncture
Intervention Description
100 patients receive verum acupuncture treatment once every other day,choosing Dazhui(GV14), Fengmen(BL12), Feishu(BL13), needles retention for 30 minutes and no moxibustion or electrical stimulation. Patients receive verum acupuncture once every other day with a total of 20 sessions in 6 weeks. The needle brand is Hwato®™ Sterile Acupuncture Needles for Single Use.
Intervention Type
Device
Intervention Name(s)
Sham acupuncture
Intervention Description
100 patients receive sham acupuncture treatment once every other day, choosing Jinsuo(DU08), Ganshu(BL18), Danshu(BL19), needles retention for 30 minutes and no moxibustion or electrical stimulation. Patients receive sham acupuncture once every other day with a total of 20 sessions in 6 weeks. The needle brand is Hwato®™ Sterile Acupuncture Needles for Single Use.
Primary Outcome Measure Information:
Title
Total score Change from Baseline of Asthma Control Test
Time Frame
Measured during the 6 week treatment period
Secondary Outcome Measure Information:
Title
Percentage of symptom-free days
Time Frame
Measured during the 6 week treatment period
Title
Usage of salbutamol and prednisone
Time Frame
Measured during the 6 week treatment period
Title
Lung function(FEV1, PVC, FEV1/FVC%, FEV1/predicted%),morning/evening PEF
Time Frame
Measured during the 6 week treatment period
Title
Asthma symptom scores
Time Frame
Measured during the 6 week treatment period
Title
Asthma quality of Life Questionnaire(AQLQ)
Time Frame
Measured during the 6 week treatment period
Title
Total number of exacerbations that require systemic corticosteroid therapy
Time Frame
Measured during the 6 week treatment period
Title
Eosinophil (EOS) count in peripheral blood, T cell classification, serum cytokine levels
Time Frame
Measured during the 6 week treatment period

10. Eligibility

Sex
All
Minimum Age & Unit of Time
14 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients diagnosed with mild-to-moderate persistent asthma Forced expiratory volume in one second (FEV1) reversibility of greater than or equal to 12% following bronchodilator administration (2 puffs) Patients who have given written informed consent Exclusion Criteria: Participation in another clinical trial 1 month prior to study entry Use of systemic corticosteroids 2 weeks prior to study entry Patients with general infection, lower respiratory infection, pulmonary tuberculosis and fungal infection 1 month prior to study entry Hospitalization due to acute exacerbation 3 months prior to study entry Patients cannot stop using forbidden drugs which include inhaled corticosteroid, theophylline, long-term β2 agonist, sodium cromoglicate, leukotrienes antagonist and anticholinergic drug Patients who are allergic to albuterol and corticosteroid Patients with severe primary diseases such as cancer, cardiovascular system, liver, kidney and hematopoietic system diseases Wheeze caused by pulmonary tuberculosis, bronchiectasia and cardiac insufficiency Patients with hyperthyroidism Patients with mental illness, acrasia Female patients in pregnancy, lactation period and planning to get pregnant during the trial Any significant disorder that in the investigator's opinion, might put the patients at risk or influence the study outcomes Acupuncture contraindications: serious allergic or infectious dermatitis and hemorrhagic diseases such as thrombocytopenic purpura and hemophilia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yong-Qing Yang, Ph.D
Organizational Affiliation
Shanghai University of TCM
Official's Role
Study Chair
Facility Information:
Facility Name
University Hospital of Gansu Traditional Chinese Medicine
City
Lanzhou
State/Province
Gansu
Country
China
Facility Name
Kaifeng Traditional Chinese Medicine hospital
City
Kaifeng
State/Province
Henan
ZIP/Postal Code
475000
Country
China
Facility Name
No.3 hospital of Henan college of Traditional Chinese Medicine
City
Zhengzhou
State/Province
Henan
ZIP/Postal Code
450000
Country
China
Facility Name
Zhengzhou Traditional Chinese Medicine hospital
City
Zhengzhou
State/Province
Henan
ZIP/Postal Code
450000
Country
China
Facility Name
Xiangya Hospital of Central South University
City
Changsha
State/Province
Hunan
ZIP/Postal Code
410000
Country
China
Facility Name
Shanghai First People's Hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200030
Country
China
Facility Name
Shanghai research institute of acupuncture and meridian,Yueyang Hospital of Integrated Traditional Chinese and Western Medicine
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200030
Country
China
Facility Name
Shanghai Dachang hospital
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
201900
Country
China
Facility Name
Longhua Hospital
City
Shanghai
State/Province
Shanghai
Country
China
Facility Name
Shanghai TCM Integrated hospital
City
Shanghai
State/Province
Shanghai
Country
China
Facility Name
Shuguang Hospital
City
Shanghai
State/Province
Shanghai
Country
China
Facility Name
Wenzhou Hospital of Traditional Chinese Medicine
City
Wenzhou
State/Province
Zhejiang
Country
China

12. IPD Sharing Statement

Citations:
PubMed Identifier
26399399
Citation
Yin LM, Wang Y, Fan L, Xu YD, Wang WQ, Liu YY, Feng JT, Hu CP, Wang PY, Zhang TF, Shao SJ, Yang YQ. Efficacy of acupuncture for chronic asthma: study protocol for a randomized controlled trial. Trials. 2015 Sep 23;16:424. doi: 10.1186/s13063-015-0947-z.
Results Reference
derived

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Clinical Assessment of Acupuncture for the Treatment of Chronic Asthma

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