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Effects of external counterpulsation therapy on corticomotor excitability and motor function recovery in patients with subacute stroke

Effects of external counterpulsation therapy on corticomotor excitability and motor function recovery in patients with subacute stroke

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002531
Enrollment
Unknown
Registered
2012-09-24
Start date
2012-08-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

stroke

Interventions

Real:Real ECP
Sham:Real ECP

Sponsors

Neurology, M&T, Prince of Wales Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Subject is aged 18 or above; 2. First-ever ischaemic stroke with onset ranging from 4 to 21 days; 3. Subject is found to have upper limb motor function impairment as a result ofstroke; 4. Subject has brain CT performed and results confirmed no evidence ofintracerebral haemorrhage; 5. NIHSS is less than 10; 6. Subject or his/her legally acceptable representative is willing to provide writteninformed consent.

Exclusion criteria

Exclusion criteria: 1. Personal or family history of epilepsy; 2. Metal implant(s) in any part of body or head (excluding tooth fillings); 3. Implanted cardiac pacemaker, defibrillator, medication pump or any other implanted electronics; 4. Personal history of recurring headaches; 5. History of skull fracture, serious head injury, and any head or brain surgery; 6. History of malignancy; 7. Evidence for cardioembolic stroke such as atrial fibrillation and rheumatic heart disease; 8. Sustained hypertension (systolic >180mmHg or diastolic > 100mmHg); 9. Subject has thrombocytopenia (platelet count 300 µmol/L, if known), cirrhosis, severe dementia or psychosis. 12. Subject has brain tumour or other significant non-ischaemic brain lesion on CT. Version 1.0 31/05/2012 13. Subject is unlikely to be followed up at one month later . 14. Subject is a pregnant female or a breast-feeding mother.

Design outcomes

Primary

MeasureTime frame
RMT;AMPLITUDE;LATENCY;POWER GRIP;LATERAL PINCH GRIP;LATERAL PINCH GRIP;PURDUE PEGBOARD;NIHSS;MRS;

Countries

China

Contacts

Public ContactLawrence K.S. WONG
ks-wong@cuhk.edu.hk+852 2632 3877

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026