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Acupuncture in Persistent Atrial Fibrillation

Primary Purpose

Persistent Atrial Fibrillation

Status
Unknown status
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Active Acupuncture
Sham acupuncture
flecainide
Sponsored by
Kyunghee University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Persistent Atrial Fibrillation focused on measuring Atrial fibrillation, Acupuncture, Recurrence, Electrical cardioversion

Eligibility Criteria

20 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Persistent AF lasting ≥ 7 days
  • Ages in 20-75 years
  • Resistant with antiarrhythmic drugs
  • Written informed consent

Exclusion Criteria:

  • Age below 20 years or above 75 years
  • Severe valvular heart disease
  • History of open heart surgery
  • History of treatment for myocardial infarction (MI) within recent 6 weeks
  • Patients under or requiring the administration of antiviral drugs
  • 2nd degree atrioventricular block or more than two fascicular block
  • Severe pulmonary, liver, or renal disease
  • Previous acupuncture treatment for cardiovascular condition within 3 months

Sites / Locations

  • Kyung Hee University Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Sham Comparator

Arm Label

Active Acupuncture + flecainide

Sham acupuncture + flecainide

Arm Description

The participants in this group receive verum acupuncture treatment once a week for 10 weeks and flecainide 75 mg twice daily.

The participants in this group receive sham acupuncture treatment once a week for 10 weeks and flecainide 75 mg twice daily.

Outcomes

Primary Outcome Measures

Recurrence of atrial fibrillation evaluated on serial electrocardiography and 48 hour holter monitoring after sinus conversion by electrical cardioversion
When patient feel symptoms such as palpitation and chest discomfort, the patients are recommended to visit hospital to check out the recurrence of atrial fibrillation.

Secondary Outcome Measures

Changes in function and volume of left atrium and left atrial appendage evaluated by echocardiography
Change of inflammation marker (hsCRP)
Other markers can be added
Number of Participants with Adverse Events (AEs)
All participants and practitioners are taught to report any AEs. If there are any AEs, the following items are recorded by practitioners at each visit and appropriate actions are taken: type of AEs, occurrence date, lost date, frequency of occurrence, severity, causality with the treatment, actions taken with the acupuncture intervention, and actions taken to the participants. Serious AEs, i.e. death or life-threatening events which are required urgent intervention, will be noted to the principal investigators immediately and determine whether the participants are dropped out.
the factor to make atrial fibrillation recur
we will perform multivariate regression analysis to know which factor makes atrial fibrillation recur irrespective of intervention method.

Full Information

First Posted
April 6, 2014
Last Updated
April 8, 2014
Sponsor
Kyunghee University Medical Center
Collaborators
Ministry of Health & Welfare, Korea
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1. Study Identification

Unique Protocol Identification Number
NCT02110537
Brief Title
Acupuncture in Persistent Atrial Fibrillation
Official Title
Clinical Trial to Evaluate the Antiarrhythmic Effects of Acupuncture for Drug Resistant Persistent Atrial Fibrillation: Randomized, Participant and Assessor Blinded, Sham-controlled, Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2014
Overall Recruitment Status
Unknown status
Study Start Date
March 2014 (undefined)
Primary Completion Date
July 2015 (Anticipated)
Study Completion Date
July 2015 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Kyunghee University Medical Center
Collaborators
Ministry of Health & Welfare, Korea

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this trial is to evaluate the effect of acupuncture on prevention of atrial fibrillation (AF) recurrence after electrical cardioversion (EC) for persistent AF patients resistant to the antiarrhythmic drugs (AADs).
Detailed Description
This is a multicenter, prospective, participant and assessor blinded, randomized, sham-controlled clinical trial with 2 parallel arms. To evaluate the efficacy and safety of acupuncture, a total of 80 persistent AF participants will be recruited and randomly assigned to active acupuncture and sham acupuncture group. Both group commonly take antiarrhythmic medication during study period. These patients who are resistant to drug therapy will get a electrical cardioversion. After cardioversion, the recurrence rate and duration of atrial fibrillation free time will be evaluated. This trial consists of 2 weeks of observation and medical therapy, 2 weeks of acupuncture intervention before EC, EC and acupuncture intervention, 7 weeks of additional intervention, and 5 weeks of follow-up. After randomization, participants receive 10 sessions of acupuncture treatments over 10 weeks. The outcome is assessed at 2, 4, 6, 8, and 16 week after randomization.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Persistent Atrial Fibrillation
Keywords
Atrial fibrillation, Acupuncture, Recurrence, Electrical cardioversion

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Active Acupuncture + flecainide
Arm Type
Experimental
Arm Description
The participants in this group receive verum acupuncture treatment once a week for 10 weeks and flecainide 75 mg twice daily.
Arm Title
Sham acupuncture + flecainide
Arm Type
Sham Comparator
Arm Description
The participants in this group receive sham acupuncture treatment once a week for 10 weeks and flecainide 75 mg twice daily.
Intervention Type
Procedure
Intervention Name(s)
Active Acupuncture
Intervention Description
Active acupuncture treatment group consists of electroacupuncture (EA) and intradermal acupuncture (IDA). For EA treatment, unilateral PC5, PC6, ST36, and ST37 are chosen. Disposable, sterile needles and low frequency electrical stimulator (ES-160, ITO, Japan) are used. Each needle is inserted to the depth of 2 ± 0.5 cm with a 90 degree angle. Thereafter, needles are connected with the pole and electrical stimulation is applied with 2Hz, continuous wave current for 20 minutes. For IDA treatment, bilateral HT7 and TF4 are selected. Disposable, sterile, sticker-type needles (0.18 mm x 1.3 mm x 1.5mm) are used. Attached needles are maintained as long as possible.
Intervention Type
Procedure
Intervention Name(s)
Sham acupuncture
Intervention Description
For sham intervention, nonacupuncture points are used. As with active treatment group, two types of acupuncture, sham EA and sham IDA, compose the sham intervention. Electrical acupuncture is connected but electrical stimulation is not given to sham acupuncture group.
Intervention Type
Drug
Intervention Name(s)
flecainide
Other Intervention Name(s)
tambocor
Intervention Description
Both groups commonly take antiarrhythmic medication (flecainide 75 mg twice daily) during study period. Flecainide administration is initiated 2 weeks before electrical cardioversion and maintain during follow up period.
Primary Outcome Measure Information:
Title
Recurrence of atrial fibrillation evaluated on serial electrocardiography and 48 hour holter monitoring after sinus conversion by electrical cardioversion
Description
When patient feel symptoms such as palpitation and chest discomfort, the patients are recommended to visit hospital to check out the recurrence of atrial fibrillation.
Time Frame
3 months after electrical cardioversion
Secondary Outcome Measure Information:
Title
Changes in function and volume of left atrium and left atrial appendage evaluated by echocardiography
Time Frame
3 months after electrical cardioversion
Title
Change of inflammation marker (hsCRP)
Description
Other markers can be added
Time Frame
3 months after electrical cardioversion
Title
Number of Participants with Adverse Events (AEs)
Description
All participants and practitioners are taught to report any AEs. If there are any AEs, the following items are recorded by practitioners at each visit and appropriate actions are taken: type of AEs, occurrence date, lost date, frequency of occurrence, severity, causality with the treatment, actions taken with the acupuncture intervention, and actions taken to the participants. Serious AEs, i.e. death or life-threatening events which are required urgent intervention, will be noted to the principal investigators immediately and determine whether the participants are dropped out.
Time Frame
Participants will be followed for the duration of this study, an expected average 14 weeks
Title
the factor to make atrial fibrillation recur
Description
we will perform multivariate regression analysis to know which factor makes atrial fibrillation recur irrespective of intervention method.
Time Frame
3 months later after electrical cardioversion

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Persistent AF lasting ≥ 7 days Ages in 20-75 years Resistant with antiarrhythmic drugs Written informed consent Exclusion Criteria: Age below 20 years or above 75 years Severe valvular heart disease History of open heart surgery History of treatment for myocardial infarction (MI) within recent 6 weeks Patients under or requiring the administration of antiviral drugs 2nd degree atrioventricular block or more than two fascicular block Severe pulmonary, liver, or renal disease Previous acupuncture treatment for cardiovascular condition within 3 months
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Weon Kim, Professor
Phone
82-2-958-8176
Email
mylovekw@hanmail.net
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Weon Kim, Professor
Organizational Affiliation
Kyunghee University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kyung Hee University Medical Center
City
Seoul
State/Province
Dongdaemun-gu
ZIP/Postal Code
130-701
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Weon Kim, Professor
Phone
82-2-958-8176
Email
mylovekw@hanmail.net
First Name & Middle Initial & Last Name & Degree
Weon Kim, Professor

12. IPD Sharing Statement

Citations:
PubMed Identifier
28159849
Citation
Lee SM, Leem J, Park JH, Yoon KH, Woo JS, Lee JM, Kim JB, Kim W, Lee S. Close look at the experiences of patients enrolled in a clinical trial of acupuncture treatment for atrial fibrillation in Korea: a qualitative study nested within a randomised controlled trial. BMJ Open. 2017 Feb 3;7(2):e013180. doi: 10.1136/bmjopen-2016-013180. Erratum In: BMJ Open. 2017 Feb 22;7(2):e013180corr1.
Results Reference
derived
PubMed Identifier
25784948
Citation
Park J, Kim HS, Lee SM, Yoon K, Kim WS, Woo JS, Lee S, Kim JB, Kim W. Acupuncture antiarrhythmic effects on drug refractory persistent atrial fibrillation: study protocol for a randomized, controlled trial. Evid Based Complement Alternat Med. 2015;2015:613970. doi: 10.1155/2015/613970. Epub 2015 Feb 17.
Results Reference
derived

Learn more about this trial

Acupuncture in Persistent Atrial Fibrillation

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