Acupuncture Treatment for Patients Who Develop Arrhythmias in the Post-Operative Cardio-Thoracic Setting



Status:Recruiting
Conditions:Atrial Fibrillation
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:18 - Any
Updated:3/9/2019
Start Date:July 26, 2018
End Date:December 2020
Contact:Dr. Chaim Locker, M.D.
Email:LekerLocker.Chaim@mayo.edu
Phone:507-255-7110

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The Feasibility of Acupuncture Treatment in the Post-Operative Cardio-Thoracic Setting for Arrhythmias in Patients Undergoing Open Heart Surgery- A Pilot Study

A feasibility study on the provision of acupuncture treatment in the hospital to 20 patients
who have undergone open heart surgery procedures. The acupuncture treatments may begin as
early as postoperative Day 2.

Primary Aim • Evaluate the feasibility of providing acupuncture in the hospital setting for
20 patients undergoing open heart surgery and subsequently develop arrhythmias.

Secondary Aims

• Evaluate the short-term effect of acupuncture including the effects on patient's
arrhythmias, stress, anxiety, and pain measured by Electrocardiogram monitoring and
Electrocardiography, VAS scores, and WIWI questionnaire for the patient.

Inclusion Criteria:

1. Patients who have undergone CABG and/or cardiac valve operations.

2. Patients developing postoperative atrial fibrillation, and documented by ECG prior to
acupuncture intervention, and treated with the common anti arrhythmic treatment of the
department.

3. Patients moving to the step-down unit on postoperative day 2 or later.

4. Ability to provide informed consent.

5. Ability to speak English and complete all aspects of this trial.

6. At least 18 years of age.

Exclusion Criteria:

1. Patients with any other cardiac or non-cardiac concomitant procedures.

2. Patients with suspected sternal wound infection and/or with prolonged sternal wound
dressing and wound- Vac-system application or open chest wound.

3. Patients with abnormal postoperative track staying in the intensive care unit for any
clinical reason or hemodynamic compromise.

4. Patients with platelet count <50,000

5. Patients in a severe immunocompromised state.

6. Pregnant women. All patients who meet the criteria will have their medical records
reviewed to ensure they are not pregnant.
We found this trial at
1
site
200 First Street SW
Rochester, Minnesota 55905
507-284-2511
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