Electroacupuncture for Heart Protection: Clinical Application in Patients Undergoing Cardiac Bypass Surgery
NCT ID: NCT05514067
Last Updated: 2024-10-29
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
10 participants
INTERVENTIONAL
2020-07-09
2023-11-14
Brief Summary
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Detailed Description
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This study aims to show the benefit of EA at cardiac-related acupoints in reducing injury to the heart in terms of less PMI in patients undergoing CABG surgery and also test the possibility that EA will have benefits in other organs in terms of less acute kidney injury and preserved cognitive function, given that the blood-borne humoral factors generated by EA may also be reno- and neuroprotective. As such, the findings for this research proposal will build on evidence for the safety and efficacy of EA in the clinical setting of CABG surgery for the benefit of patients with CAD. The expected clinical benefits of reducing PMI will include improvement in short term clinical outcomes in terms of preserving LV systolic function, preventing the onset of heart failure, and improving quality of life in patients undergoing CABG surgery. This study also intends to identify and assess the cardioprotective humoral factors generated by EA at cardiac-related acupoints in stable CAD and CABG patients, providing novel therapeutic strategies for cardioprotection. In this regard, the findings from this research proposal will add new knowledge in the field of EA cardioprotection.
60 stable CAD patients undergoing planned CABG surgery will be randomized to receive either EA at cardiac-related acupoints (N=30) or standard care (N=30). A single application of EA at cardiac-related acupoints will be administered for 30 min prior to surgery. For 10 recruited CABG patients administered EA, blood samples will be collected prior to and immediately following EA, and subjected to plasma proteomics analysis to identify the factor(s) which mediate EA cardioprotection. PMI will be measured as the 48-hour area under-the-curve serum high-sensitive Troponin-T. Blood samples will be taken at pre-op and 6, 12, 24, 48 hours (post-coming off cardiac bypass) for this evaluation.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Electro-acupuncture (EA) arm
Patients with stable CAD going for coronary artery bypass graft (CABG) surgery randomized to receive EA before surgery.
Electro-Acupuncture
A single application of EA at cardiac-related acupoints administered for 30 min prior to CABG surgery.
Standard Care arm
Patients with stable CAD going for coronary artery bypass graft (CABG) surgery.
No interventions assigned to this group
Interventions
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Electro-Acupuncture
A single application of EA at cardiac-related acupoints administered for 30 min prior to CABG surgery.
Eligibility Criteria
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Inclusion Criteria
* Patients aged 21 years and above.
Exclusion Criteria
* Patients with significant hepatic dysfunction (If available, INR\>2)
* Patients with significant pulmonary disease (If available, FEV1\<40% predicted). - Patients with known renal failure with a GFR≤30 mL/min/1.73 m2.
* Patients recruited into another study which may impact on this study.
21 Years
ALL
No
Sponsors
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National Heart Centre Singapore
OTHER
Responsible Party
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Principal Investigators
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Derek Hausenloy, PHD
Role: PRINCIPAL_INVESTIGATOR
National Heart Centre Singapore
Locations
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National Heart Centre Singapore
Singapore, , Singapore
Countries
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Other Identifiers
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2020/2028
Identifier Type: -
Identifier Source: org_study_id
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