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Effectiveness of ECP Therapy in Stable Angina Pectoris Patients

Primary Purpose

Counterpulsation, Angina Pectoris

Status
Recruiting
Phase
Not Applicable
Locations
Indonesia
Study Type
Interventional
Intervention
External Counter Pulsation (ECP) therapy
Sponsored by
Universitas Padjadjaran
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Counterpulsation focused on measuring External Counterpulsation, Stable Angina Pectoris, Indicated CABG, Global longitudinal strain, Ischemic response

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age >= 18 years old
  • Diagnosed with stable angina pectoris
  • Anatomic vessel disease (VD) lesion with 2VD/3VD
  • Indicated CABG and in waiting list of CABG procedure
  • Not planned to urgent CABG
  • Minimum optimal medical therapy within 1 week

Exclusion Criteria:

  • Congestive Heart Failure
  • LVEF <35%
  • Unprotected left main stenosis >50%
  • Blood pressure >180/110mmHg
  • Acute coronary syndrome
  • Acute Heart Failure
  • Severe aorta regurgitation
  • Malignant arrhythmia
  • Atrial fibrillation
  • Premature ventricular complex
  • Peripheral occlusive artery disease
  • Phlebitis
  • Deep vein thrombosis
  • Hemorrhagic diathesis
  • Severe chronic kidney disease
  • Aortic aneurysm
  • Abdominal aneurysm
  • Pregnancy
  • Registered as other clinical study participant

Sites / Locations

  • Dr. Hasan Sadikin General HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Intervention

Control

Arm Description

The intervention arm will comprise study participants who receive intervention therapy (i.e eligible stable angina pectoris patients in intervention arm who agree to participate)

Eligible stable angina pectoris patients in the control arm will receive no intervention therapy

Outcomes

Primary Outcome Measures

Change in Global Longitudinal Strain (GLS)
GLS is a parameter captured through transthoracic echocardiography. GLS was calculated as the mean peak longitudinal systolic strain of all the LV segments, consistent with American Society of Echocardiography (ASE) guidelines.
Change in Left Ventricular Ejection Fraction (LVEF)
LVEF is a parameter captured through transthoracic echocardiography. LVEF was calculated by Simpson biplane method
Change in Time to mm ST-segment Depression
Time to induce significant ST-segment Depression using treadmill exercise test
Change in Duration of Treadmill Test
Maximally tolerated time of treadmill exercise test using Bruce protocol or Modified Bruce protocol
Change in CCS score
Degree of presenting chest pain symptoms using the Canadian cardiovascular society (CCS) class score. CCS class score ranging from 1 (mild) to 4 (severe)
Change in Seattle Angina Questionnaire (SAQ) Score
Quality of life based on The Seattle Angina Questionnaire measurement. The possible range of scores for each of the five subscales is 0 to 100, with higher scores indicating better quality of life. A change of 10 points in any of the subscales is considered to be clinically important.

Secondary Outcome Measures

Change in Summed Rest Score (SRS)
Summed Rest Score is part of myocardial perfusion parameters of SPECT myocardial perfusion defects examination. The score are accumulated from 17 polar map segment. each segment scored. the extent and severity of perfusion deficits while rest ranging from 0 to 4 with higher score mean worse clinical apperance.
Change in Summed Stress Score (SSS)
Summed Stress Score is part of myocardial perfusion parameters of SPECT myocardial perfusion defects examination. The score are accumulated from 17 polar map segment. each segment scored. the extent and severity of perfusion deficits while stress ranging from 0 to 4 with higher score mean worse clinical apperance.
Change in Summed Difference Score (SDS)
Summed Difference Score is part of myocardial perfusion parameters of SPECT myocardial perfusion defects examination. SDS can be calculated by subtracting the SRS from the SSS (SDS = SSS - SRS). This measure is used to describe the degree to which the deficit/ischemia is reversible. An SDS score of 0-1 indicates no ischemia; 2-4 points indicate mild ischemia; 5-6 points indicate moderate ischemia; while 7 or more points indicate severe ischemia.
Myocardial Micro-alternation Index (MMI)
Myocardial Micro-alternation Index is part of ECG dispersion mapping (ECG-DM)
The level of Vascular Endothelial Growth Factor (VEGF)
Blood tests were carried out to determine levels of VEGF using ELISA and quantitative reverse transcription-polymerase chain reaction (qRT-PCR). The measurement unit is pg/ml.
The level of microRNA-92a (miR-92a)
Blood tests were carried out to determine levels of miR-92a using ELISA and quantitative reverse transcription-polymerase chain reaction (qRT-PCR).
The level of NT pro BNP and Troponin
Blood tests were carried out to determine levels of NT pro BNP (measurement unit pg/ml).
The level of Troponin
Blood tests were carried out to determine levels of Troponin (measurement unit ng/ml).
Change in Quality of Life
Quality of life based on Questionnaire The Indonesian EQ-5D-5L, is a questionnaire used to assess the quality of life of angina pectoris patients undergoing ECP treatment, allowing us to determine how much money can be saved in extending a patient's life for one year. It consists of five assessment domains, which are walking ability, self-care, usual activities, pain/discomfort, and anxiety/depression. The normal range is 0-1, with a score of 1 indicating the best quality of life.
Major Adverse Cardiac Event (MACE)
Number of incidence of Major adverse cardiac event
Effectiveness of ECP for stable angina pectoris patients
Effectiveness of ECP for stable angina pectoris patients is based on pharmacoeconomics. The assessment will use the ICER formula, comparing optimal medication therapy from both healthcare and national insurance perspectives, taking into account about nominal outcomes, clinical outcomes, and patient quality of life outcomes. The results from the formula will then be input into a diagram to determine whether they fall into quadrant 1, 2, 3, or 4 (the best outcome is if it falls into quadrant 2).

Full Information

First Posted
April 24, 2021
Last Updated
September 21, 2023
Sponsor
Universitas Padjadjaran
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1. Study Identification

Unique Protocol Identification Number
NCT04873687
Brief Title
Effectiveness of ECP Therapy in Stable Angina Pectoris Patients
Official Title
Effectiveness of External Counter Pulsation (ECP) Therapy in Stable Angina Pectoris Patients; a Proof of Principal Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 1, 2023 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
December 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universitas Padjadjaran

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
External Counterpulsation (ECP) is a non-invasive therapy using pressured cuff that is performed on patients with refractory stable angina pectoris to relieve symptoms and increase quality of life. In Indonesia, waiting time for getting coronary artery bypass grafting (CABG) procedure for revascularization treatment in stable angina pectoris patients is way longer than international recommendation which correlates with increase morbidity and mortality during the waiting time. Utilization of ECP for such patients who wait for CABG procedure is still unclear. The investigator aim to evaluate efficacy of addition of ECP compared with medical therapy alone for this population. The efficacy is evaluated using measurement from echocardiography result, treadmill test result, and clinical outcome. if applicable, examination of myocardial perfusion using nuclear examination will also be performed.
Detailed Description
Waiting time for elective CABG procedure in Indonesia is usually longer than six weeks, way longer than the European society of cardiology recommendation. During the waiting time, patients still complain of having troubling chest pain and at risk from 1.7% mortality even after optimal medical therapy. ECP is a non-invasive therapy using a pressured cuff performed on patients that have been utilized in refractory angina pectoris patients to relieve symptoms, increase the quality of life, and decrease future major adverse cardiac events (MACE). This study is proof of principal clinical trial to evaluate the efficacy of addition ECP therapy after optimal medical therapy for stable angina pectoris patients waiting for CABG in Dr. Hasan Sadikin General Hospital, Bandung, Indonesia. Eligible patients will be informed about the study and randomized to the intervention arm. Patients in the experimental arm will undergo ECP therapy consisting of 36 sessions, each session @1 hour/day, five days a week with an initial pressure of 300mmHg. No intervention will be given to patients in the control arm. The primary and secondary endpoint is the change in variables measured before and after the intervention is fully implemented. The primary endpoint variables are global longitudinal strain (GLS), Left ventricular ejection fraction (LVEF), Time to ST-Segment depression, duration of treadmill test, the Canadian cardiovascular society (CCS) score, and the Seattle angina questionnaire (SAQ) score. The secondary endpoint variable will be myocardial perfusion score measured as Summed Rest Score, Summed Stress Score, Summed Difference Score, Myocardial Micro-alternation Index (MMI), the level of Vascular Endothelial Growth Factor (VEGF), microRNA-92a (miR-92a), NT pro BNP, Troponin, incidence of MACE, general quality of life based on questionnaire The Indonesian EQ-5D-5L, and effectiveness of ECP for stable angina pectoris patients with pharmaco-economy studies. This change will then be compared between the intervention experimental arm and control arm. Safety oversight by a Data and Safety Monitoring Board (DSMB) will be conducted by independent parties. Internal Data Monitoring Committee (DMC) will be established to oversee the study, focused on data quality. Quality control (QC) procedures will be implemented beginning with the data entry system. Data QC checks that will be run on the database will be automatically generated weekly, and any quality issues identified will be reviewed by the DMC a plan put in place for resolution.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Counterpulsation, Angina Pectoris
Keywords
External Counterpulsation, Stable Angina Pectoris, Indicated CABG, Global longitudinal strain, Ischemic response

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The intervention will be administered to eligible stable angina pectoris patients Dr. Hasan Sadikin General Hospital in a randomized manner neither of experiment or control group.
Masking
Outcomes Assessor
Masking Description
Outcome assessor and study statistician will not be aware of intervention assignment
Allocation
Randomized
Enrollment
84 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Intervention
Arm Type
Experimental
Arm Description
The intervention arm will comprise study participants who receive intervention therapy (i.e eligible stable angina pectoris patients in intervention arm who agree to participate)
Arm Title
Control
Arm Type
No Intervention
Arm Description
Eligible stable angina pectoris patients in the control arm will receive no intervention therapy
Intervention Type
Device
Intervention Name(s)
External Counter Pulsation (ECP) therapy
Intervention Description
ECP therapy consist of 36 session, each session @1 hour/day, five days a week with initial pressure of 300mmHg
Primary Outcome Measure Information:
Title
Change in Global Longitudinal Strain (GLS)
Description
GLS is a parameter captured through transthoracic echocardiography. GLS was calculated as the mean peak longitudinal systolic strain of all the LV segments, consistent with American Society of Echocardiography (ASE) guidelines.
Time Frame
At baseline and week 7 (post intervention)
Title
Change in Left Ventricular Ejection Fraction (LVEF)
Description
LVEF is a parameter captured through transthoracic echocardiography. LVEF was calculated by Simpson biplane method
Time Frame
At baseline and week 7 (post intervention)
Title
Change in Time to mm ST-segment Depression
Description
Time to induce significant ST-segment Depression using treadmill exercise test
Time Frame
At baseline and week 7 (post intervention)
Title
Change in Duration of Treadmill Test
Description
Maximally tolerated time of treadmill exercise test using Bruce protocol or Modified Bruce protocol
Time Frame
At baseline and week 7 (post intervention)
Title
Change in CCS score
Description
Degree of presenting chest pain symptoms using the Canadian cardiovascular society (CCS) class score. CCS class score ranging from 1 (mild) to 4 (severe)
Time Frame
At baseline and week 7 (post intervention)
Title
Change in Seattle Angina Questionnaire (SAQ) Score
Description
Quality of life based on The Seattle Angina Questionnaire measurement. The possible range of scores for each of the five subscales is 0 to 100, with higher scores indicating better quality of life. A change of 10 points in any of the subscales is considered to be clinically important.
Time Frame
At baseline and week 7 (post intervention)
Secondary Outcome Measure Information:
Title
Change in Summed Rest Score (SRS)
Description
Summed Rest Score is part of myocardial perfusion parameters of SPECT myocardial perfusion defects examination. The score are accumulated from 17 polar map segment. each segment scored. the extent and severity of perfusion deficits while rest ranging from 0 to 4 with higher score mean worse clinical apperance.
Time Frame
At baseline and week 7 (post intervention)
Title
Change in Summed Stress Score (SSS)
Description
Summed Stress Score is part of myocardial perfusion parameters of SPECT myocardial perfusion defects examination. The score are accumulated from 17 polar map segment. each segment scored. the extent and severity of perfusion deficits while stress ranging from 0 to 4 with higher score mean worse clinical apperance.
Time Frame
At baseline and week 7 (post intervention)
Title
Change in Summed Difference Score (SDS)
Description
Summed Difference Score is part of myocardial perfusion parameters of SPECT myocardial perfusion defects examination. SDS can be calculated by subtracting the SRS from the SSS (SDS = SSS - SRS). This measure is used to describe the degree to which the deficit/ischemia is reversible. An SDS score of 0-1 indicates no ischemia; 2-4 points indicate mild ischemia; 5-6 points indicate moderate ischemia; while 7 or more points indicate severe ischemia.
Time Frame
At baseline and week 7 (post intervention)
Title
Myocardial Micro-alternation Index (MMI)
Description
Myocardial Micro-alternation Index is part of ECG dispersion mapping (ECG-DM)
Time Frame
At baseline and week 7 (post intervention)
Title
The level of Vascular Endothelial Growth Factor (VEGF)
Description
Blood tests were carried out to determine levels of VEGF using ELISA and quantitative reverse transcription-polymerase chain reaction (qRT-PCR). The measurement unit is pg/ml.
Time Frame
At baseline and week 7 (post intervention)
Title
The level of microRNA-92a (miR-92a)
Description
Blood tests were carried out to determine levels of miR-92a using ELISA and quantitative reverse transcription-polymerase chain reaction (qRT-PCR).
Time Frame
At baseline and week 7 (post intervention)
Title
The level of NT pro BNP and Troponin
Description
Blood tests were carried out to determine levels of NT pro BNP (measurement unit pg/ml).
Time Frame
At baseline and week 7 (post intervention)
Title
The level of Troponin
Description
Blood tests were carried out to determine levels of Troponin (measurement unit ng/ml).
Time Frame
At baseline and week 7 (post intervention)
Title
Change in Quality of Life
Description
Quality of life based on Questionnaire The Indonesian EQ-5D-5L, is a questionnaire used to assess the quality of life of angina pectoris patients undergoing ECP treatment, allowing us to determine how much money can be saved in extending a patient's life for one year. It consists of five assessment domains, which are walking ability, self-care, usual activities, pain/discomfort, and anxiety/depression. The normal range is 0-1, with a score of 1 indicating the best quality of life.
Time Frame
At baseline and week 7 (post intervention)
Title
Major Adverse Cardiac Event (MACE)
Description
Number of incidence of Major adverse cardiac event
Time Frame
2 years
Title
Effectiveness of ECP for stable angina pectoris patients
Description
Effectiveness of ECP for stable angina pectoris patients is based on pharmacoeconomics. The assessment will use the ICER formula, comparing optimal medication therapy from both healthcare and national insurance perspectives, taking into account about nominal outcomes, clinical outcomes, and patient quality of life outcomes. The results from the formula will then be input into a diagram to determine whether they fall into quadrant 1, 2, 3, or 4 (the best outcome is if it falls into quadrant 2).
Time Frame
At baseline and week 7 (post intervention)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age >= 18 years old Diagnosed with stable angina pectoris Anatomic vessel disease (VD) lesion with 2VD/3VD Indicated for CABG and in waiting list of CABG procedure; or refuse for CABG and choose medical therapy only; or patients who are decided by the responsible doctor for medical treatment alone because of the high risks of CABG surgery. Not planned to urgent CABG Minimum optimal medical therapy within 2 weeks Able and willing to sign informed consent and comply with study procedures The patient lives in Bandung City and its neighborhood Retired patient; or not actively working during working hours; or willing to take the time to participate in research. Exclusion Criteria: Congestive Heart Failure Chronic heart failure with Functional Class NYHA III - IV LVEF <35% Unprotected left main stenosis >50% Blood pressure >180/110mmHg Acute coronary syndrome Acute Heart Failure Severe aorta regurgitation Malignant arrhythmia Atrial fibrillation Premature ventricular complex Peripheral occlusive artery disease Phlebitis Deep vein thrombosis Hemorrhagic diathesis Severe chronic kidney disease Aortic aneurysm Abdominal aneurysm Osteoarthritis Low back pain Pregnancy Registered as other clinical study participant
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mohammad R Akbar, MD, FIHA.
Phone
+6281221040265
Email
m.r.akbar@unpad.ac.id
First Name & Middle Initial & Last Name or Official Title & Degree
Badai B Tiksnadi, MD, FIHA.
Phone
+628112237277
Email
badai.bhatara.tiksnadi@unpad.ac.id
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mohammad R Akbar, MD, FIHA.
Organizational Affiliation
Universitas Padjadjaran
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dr. Hasan Sadikin General Hospital
City
Bandung
State/Province
West Java
ZIP/Postal Code
40161
Country
Indonesia
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Badai B Tiksnadi, MD, FIHA
Phone
+62112237277
Email
badai.bhatara.tiksnadi@unpad.ac.id
First Name & Middle Initial & Last Name & Degree
Badai B Tiksnadi, MD, FIHA

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
10362181
Citation
Arora RR, Chou TM, Jain D, Fleishman B, Crawford L, McKiernan T, Nesto RW. The multicenter study of enhanced external counterpulsation (MUST-EECP): effect of EECP on exercise-induced myocardial ischemia and anginal episodes. J Am Coll Cardiol. 1999 Jun;33(7):1833-40. doi: 10.1016/s0735-1097(99)00140-0.
Results Reference
background
PubMed Identifier
31929322
Citation
Wu E, Desta L, Brostrom A, Martensson J. Effectiveness of Enhanced External Counterpulsation Treatment on Symptom Burden, Medication Profile, Physical Capacity, Cardiac Anxiety, and Health-Related Quality of Life in Patients With Refractory Angina Pectoris. J Cardiovasc Nurs. 2020 Jul/Aug;35(4):375-385. doi: 10.1097/JCN.0000000000000638.
Results Reference
background
PubMed Identifier
27891374
Citation
Subramanian R, Nayar S, Meyyappan C, Ganesh N, Chandrakasu A, Nayar PG. Effect of Enhanced External Counter Pulsation Treatment on Aortic Blood Pressure, Arterial Stiffness and Ejection Fraction in Patients with Coronary Artery Disease. J Clin Diagn Res. 2016 Oct;10(10):OC30-OC34. doi: 10.7860/JCDR/2016/23122.8743. Epub 2016 Oct 1.
Results Reference
background
PubMed Identifier
26632696
Citation
Zhang C, Liu X, Wang X, Wang Q, Zhang Y, Ge Z. Efficacy of Enhanced External Counterpulsation in Patients With Chronic Refractory Angina on Canadian Cardiovascular Society (CCS) Angina Class: An Updated Meta-Analysis. Medicine (Baltimore). 2015 Nov;94(47):e2002. doi: 10.1097/MD.0000000000002002.
Results Reference
background
PubMed Identifier
28472484
Citation
Head SJ, da Costa BR, Beumer B, Stefanini GG, Alfonso F, Clemmensen PM, Collet JP, Cremer J, Falk V, Filippatos G, Hamm C, Kappetein AP, Kastrati A, Knuuti J, Kolh P, Landmesser U, Laufer G, Neumann FJ, Richter DJ, Schauerte P, Taggart DP, Torracca L, Valgimigli M, Wijns W, Witkowski A, Windecker S, Juni P, Sousa-Uva M. Adverse events while awaiting myocardial revascularization: a systematic review and meta-analysis. Eur J Cardiothorac Surg. 2017 Aug 1;52(2):206-217. doi: 10.1093/ejcts/ezx115.
Results Reference
background
PubMed Identifier
26932695
Citation
Rampengan SH, Prihartono J, Siagian M, Immanuel S. The Effect of Enhanced External Counterpulsation Therapy and Improvement of Functional Capacity in Chronic Heart Failure patients: a Randomized Clinical Trial. Acta Med Indones. 2015 Oct;47(4):275-82.
Results Reference
background
Links:
URL
https://inaheart.org/storage/guideline/199be18f2d457424b6e83ef063b64ffa.pdf
Description
Indonesian Heart Association Guidelines for External Counterpulsation Therapy for Patients with Cardiovascular Disease

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Effectiveness of ECP Therapy in Stable Angina Pectoris Patients

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