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Effect of External Counter Pulsation on Ischemic Stroke

Effect of External Counter Pulsation on IschemicStroke (ECP-STROKE)

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03075137
Enrollment
380
Registered
2017-03-09
Start date
2018-06-10
Completion date
2019-06-30
Last updated
2017-12-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ischemic Stroke

Keywords

ischemic stroke, external counter pulsation, mRS

Brief summary

Stroke is a prevalent atherosclerosis vascular disease with high mortality, external counter pulsation (ECP) is an approved noninvasive therapy for angina, congestive heart failure, myocardial infarction, and cardiogenic shock that augments blood flow to cardiac and systemic circuits, which improves the flow volume in the carotid. Though ECP is Ⅱa recommendation for stroke management, no multi-center control clinical study has been reported for prognosis of stroke. The aim of this study is to evaluate the effect of ECP on stoke. To address this assumption, investigators enroll subjects with ischemic stroke and randomized into control or ECP group, the ECP intervention will be carried out with a standard protocol which involves 35 one-hour sessions (5 days a week) for continuous 7 weeks. The primary endpoint is mRS score in 3 months, secondary endpoints include NIHSS, BI and MMSE score, recurrence of stroke in 3 months, glycolipid metabolism, transcranial doppler (TCD) flow velocities and endothelial function.

Detailed description

Cardiovascular disease is the leading cause of mortality worldwide, accounting for 17.5 million deaths per year; 6.7 million of these deaths are related to stroke. Over 80% of strokes are classified as ischemic. External counter pulsation (ECP) is a non-invasive method which consists of three sets of pneumatic cuffs attached to each of the patient's legs at the calf and lower and upper thigh. The inflation of the cuffs is triggered by a computer, and timing of the inflation is based on the R wave of the electrocardiogram. The ECP therapist adjusts the inflation and deflation timing to provide optimal blood movement per a finger plethysmogram waveform reading. This produces a retrograde flow of blood in the aorta resulting in a diastolic augmentation of blood flow and also an increase in venous return, which leads to an improved carotid perfusion pressure. Cumulative evidences demonstrate that ECP can augment peak diastolic and mean middle cerebral artery flow velocities, accelerate rehabilitation after stroke, however, no multi-center study on the effect of ECP on the prognosis of stroke has been reported. Thus, this study is designed to enroll 380 subjects with ischemic stroke after evaluation of glycolipid metabolism, heart function, transcranial doppler (TCD) flow velocities, endothelial function, NIHSS, BI and MMSE score, they will be randomized into ECP intervention or control group. All subjects receive Guideline-driven standard medical treatment, ECP will be carried out with a standard protocol which involves 35 one-hour sessions (5 days a week) for continuous 7 weeks. Up to the end of ECP intervention, mRS of subjects will be follow up to 3 months, meanwhile, items as above will be retested for comparison.

Interventions

DEVICEExternal counter pulsation (ECP)

standard ECP protocol involves 35 one-hour sessions (once per day, 5 days a week) and continuous for 7 weeks. ECP consists of three sets of pneumatic cuffs attached to each of the patient's legs at the calf and lower and upper thigh. The inflation of the cuffs is triggered by a computer, and timing of the inflation is based on the R wave of the electrocardiogram. The ECP therapist adjusts the inflation and deflation timing to provide optimal blood movement per a finger plethysmogram waveform reading.

Sponsors

Chinese University of Hong Kong
CollaboratorOTHER
Second Affiliated Hospital of Xi'an Jiaotong University
CollaboratorOTHER
Second Affiliated Hospital of Zhengzhou University
CollaboratorOTHER
Eighth Affiliated Hospital, Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis of ischemic stroke * Exclusion cerebral hemorrhage after CT scan * NIH Stroke Scale (NIHSS)≥4 * Modified Rankin Scale (mRS) 0-1 * Signed informed consent

Exclusion criteria

* Obvious aortic insufficiency; * Aortic aneurysm or aortic dissection; * Coronary fistula or severe coronary aneurysm; * Not controlled bleeding disease with INR\>2.0 ; * Symptomatic Congestive heart failure * Valvular heart disease, congenital heart diseases, cardiomyopathies * Cerebral hemorrhage within six months; * Uncontrolled hypertension, defined as SBP≥180mmHg or DBP≥110mmHg; * Lower limb infection; * Deep venous thrombosis; * Progressive malignancies or diseases with poor prognosis

Design outcomes

Primary

MeasureTime frameDescription
modified Rankin Scale (mRS) scoreChange from Baseline at 3 months3-month mRS score after stroke

Secondary

MeasureTime frameDescription
NIH Stroke Scale (NIHSS) scoreChange from Baseline at 3 months3-month NIHSS score after stroke
Barthel Index (BI)Change from Baseline at 3 months3-month BI after stroke
mini-mental state examination (MMSE) ScoreChange from Baseline at 3 months3-month MMSE after stroke
Ischemic area of Cerebral CT imageChange from Baseline at 3 monthsIschemic area of 3-month Cerebral CT image
Transcranial doppler (TCD) flow velocitiesChange from Baseline at 3 monthstranscranial doppler (TCD) flow velocities

Countries

China

Contacts

Primary ContactGuifu Wu, PhD
wuguifu@mail.sysu.edu.cn+8615989892111
Backup ContactJianhang Du, PhD
zsudjhang@163.com+8613652851566

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026