Electroacupuncture for Heart Protection: Clinical Application in Patients Undergoing Cardiac Bypass Surgery

NCT ID: NCT05514067

Last Updated: 2024-10-29

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

10 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-07-09

Study Completion Date

2023-11-14

Brief Summary

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Coronary artery disease (CAD) is the leading cause of death and disability in Singapore and worldwide. Many patients with multi-vessel CAD require surgical revascularisation by coronary artery bypass graft (CABG) surgery, and are at risk of postsurgical complications such as peri-operative myocardial injury (PMI), left ventricular dysfunction, heart failure, and death. This risk is particularly important given that the aging population, and increased prevalence of co-morbidities (diabetes, hypertension, renal failure) and complexity of cardiac surgery, mean that higher risk patients are undergoing CABG surgery. As such, new treatment strategies are required to protect the heart during CABG surgery in order to improve health outcomes in patients with CAD. In this regard, a number of animal studies have demonstrated that electroacupuncture (EA) at cardiac-related acupoints can protect the heart against the detrimental effects of acute ischaemia/reperfusion injury (IRI). However, the mechanisms underlying the beneficial effect of EA, and whether EA can protect the heart against PMI in patients undergoing CABG surgery are not known. Therefore, in this research proposal, the investigators will investigate whether EA at cardiac-related acupoints can protect the heart against PMI during CABG surgery, and the investigators will elucidate the mechanisms underlying the cardioprotective effects of EA.

Detailed Description

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There are currently no effective therapies for protecting the heart against PMI during CABG surgery and therefore, new therapeutic interventions are required to reduce the magnitude of PMI, in order to preserve LV systolic function and improve health outcomes in CAD patients undergoing CABG surgery. In this regard, electroacupuncture (EA) may provide a novel treatment strategy for protecting the heart and reducing PMI during CABG surgery, and is investigated in this TCM research proposal. The magnitude of PMI can be quantified by measuring post-operative levels of serum cardiac biomarkers such CK-MB, Troponin-T, or Troponin-I, the release of which have been associated with worse clinical outcomes following CABG surgery.

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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Coronary Artery Disease Electro-Acupuncture

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Patients will then be randomised 1:1 to receive either the EA or standard care protocols.
Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

After obtaining consent, patient's study arm will be revealed via sequentially numbered, opaque, sealed and stapled envelopes.

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.

Group Type EXPERIMENTAL

Electro-Acupuncture

Intervention Type PROCEDURE

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.

Group Type NO_INTERVENTION

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.

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Patients with stable CAD undergoing planned CABG surgery on cardiopulmonary bypass using blood cardioplegia.
* Patients aged 21 years and above.

Exclusion Criteria

* Patients with recent myocardial infarction (\<30 days)
* 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.
Minimum Eligible Age

21 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Heart Centre Singapore

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

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

Site Status

Countries

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Singapore

Other Identifiers

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2020/2028

Identifier Type: -

Identifier Source: org_study_id

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