IMPULSE - StIMulation of Brain Plasticity to Improve Upper Limb Recovery After StrokE

NCT ID: NCT04124367

Last Updated: 2022-07-28

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE2
• Total Enrollment: 4 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-06-25
• Study Completion Date: 2022-03-21

Brief Summary

Stroke is a leading cause of adult long-term disability worldwide. Recovery of arm and hand function after stroke is limited to about 50% of patients and full recovery is achieved in only 12% of stroke survivors by 6 months after stroke. Within the first 8-12 weeks post-stroke, a proportional recovery of 70%, corresponding to good recovery, may be achieved, but at later stages no major gain is observed with current therapy practices. Accordingly, there is a need to find new potential therapeutic tools to enhance post-stroke motor recovery. Rehabilitation supported by neuroplastic intervention is a new and pragmatic therapeutic approach in the treatment of stroke, giving way to a concept of 'recovery enhancers'.

The objective of this study is to assess whether an additional therapy with Cerebrolysin and anodal transcranial direct current stimulation (atDCS) increases the success of conventional rehabilitation therapy in subacute and chronic stroke patients with unexploited potential for functional recovery despite intact structural and functional pathways in the brain.

Hypothesis:

The hypothesis is that the combination of Cerebrolysin and atDCS facilitates motor learning in subacute and chronic stroke patients. Accordingly, motor function recovery at day 21 post-baseline is expected to be higher in the verum group (conventional rehabilitation + task-specific motor training + Cerebrolysin + atDCS) as compared to the control group (conventional rehabilitation + task-specific motor training + placebo + sham-transcranial direct current stimulation).

The primary objective is to show a significantly higher proportional recovery rate in the Action Research Arm Test (ARAT) at day 21 post-baseline in the verum group as compared to the control group.

The secondary objective is to assess the impact of this neuroplastic intervention on finger dexterity (Nine-hole peg test - 9HPT), hand grip strength, and neurological deficits (National Institutes of Healths Stroke Scale - NIHSS) at the end of therapy (day 21 post-baseline). Safety data are collected throughout the study and thereafter in case of ongoing serious adverse events (SAEs) at study endpoint.

Optional secondary parameters include electroencephalography (EEG) parameters and Brain Derived Neurotrophic Factor (BDNF) status analyses to document plastic changes in the brain, in particular changes of the cortical network functionality during neurorehabilitation, and to assess the impact of neuroplastic intervention on the BDNF synthesis rate as well as the influence of different BDNF polymorphisms.

Conditions

Chronic Stroke; Subacute Stroke

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

Verum

Group Type: ACTIVE_COMPARATOR

Cerebrolysin

Intervention Type: DRUG

30 ml once daily (+70 ml 0.9% saline)

non-invasive brain stimulation

Intervention Type: DEVICE

2 mA/35 cm² for 2x20 minutes, once daily

Control

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

100 ml once daily 0.9% saline

sham intervention

Intervention Type: DEVICE

0 mA/35 cm² for 2x20 minutes, once daily Run-in phase consisting of ramp-up (10 seconds), stimulation (10 seconds), and ramp-down (10 seconds).

Interventions

Cerebrolysin

30 ml once daily (+70 ml 0.9% saline)

Intervention Type: DRUG

non-invasive brain stimulation

2 mA/35 cm² for 2x20 minutes, once daily

Intervention Type: DEVICE

Placebo

100 ml once daily 0.9% saline

Intervention Type: DRUG

sham intervention

0 mA/35 cm² for 2x20 minutes, once daily Run-in phase consisting of ramp-up (10 seconds), stimulation (10 seconds), and ramp-down (10 seconds).

Intervention Type: DEVICE

Other Intervention Names

atDCS

Eligibility Criteria

Inclusion Criteria

• 18-80 years of age, both inclusive, of all sexes
• 8 weeks to 12 months after a first-ever hemispheric subcortical ischemic stroke, confirmed by imaging
• Pre-stroke modified Rankin Scale (mRS) 0 or 1
• Action Research Arm Test (ARAT) score 13-50, both inclusive
• Shoulder Abduction Finger Extension (SAFE) score ≥5
• Patient participates voluntarily and gave written informed consent

Exclusion Criteria

Disease-related:

o Study procedures:

1. Severe sensory deficits (score of 2 on item 8 of the NIHSS)

2. Severe aphasia (a score of ≥2 on item 9 of the NIHSS)

3. Severe neglect (a score of 2 on item 11 of the NIHSS)

4. Co-morbid conditions such as fractures, osteoarthritis, fixed or severely interfering contraction or deformity in the affected limb, polyneuropathy and/or ischemic peripheral disease if the sensorimotor functions of the upper extremities are affected, other neurological disease(s) or known brain abnormalities, acute coronary syndrome, severe heart disease (NYHA class III or IV), cancer, severe liver disease (hepatic disease associated with coagulopathy [prothrombin time prolonged beyond the normal range] and clinically relevant bleeding risk including cirrhotic patients with Child Pugh B and C), and other major medical conditions that, in the opinion of the site investigator, might influence efficacy or safety assessment

5. MMSE <20

6. Current drug or alcohol use or dependency that would interfere with adherence to study procedures

7. Participation in another interventional study

• Spasticity:

8. Major spasticity as indicated by the Modified Ashworth Spasticity Scale >2/4 in either elbow flexors, wrist flexors or finger flexors of the affected limb

9. Injection of botulinum toxin to the affected upper limb in the last three months, or the need of an injection of botulinum toxin anytime during the study period

10. Injection of phenol to the affected upper limb in the last six months, or the need of an injection of phenol anytime during the study period

Exposure-related:

11. Pacemaker or brain stimulator

12. Implanted intracranial metals in the stimulation area such as clipping, coilings, ventriculo-peritoneal shunts, endoprosthesis, cochlear implant

13. Scalp wounds or infections in the area of stimulation

14. Any condition that would represent a contraindication for Cerebrolysin administration:

• hypersensitivity to one of the components of the drug
• epilepsy
• severe renal impairment (estimated glomerular filtration rate [eGFR] <30 ml/min/1.73 m2 as assessed at local laboratory within one month before screening)

15. Breastfeeding; pregnant or trying to become pregnant

16. Concomitant medications

• with potential negative effects on cortical excitability or plasticity (e.g. psycholeptics (ATC class N05), antiepileptics, neuroleptics, benzodiazepines, dextromethorphan)
• with potential positive effects on cortical excitability or plasticity (e.g. SSRIs, SNRIs, dopaminergic preparations, memantine, AChEIs, amphetamines) - except if the patient is on a stable dose for a minimum of four weeks. Special attention should be given to possible additive effects when Cerebrolysin is used in conjunction with antidepressants/MAO inhibitors. High doses of MAO inhibitors in combination with higher dosages of Cerebrolysin (30-40 ml) have been reported to increase blood pressure.
• with neuroprotective/neurotrophic/nootropic effects (e.g. ginkgo biloba, erythropoietin, citicoline, amantadine, piracetam)

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

VASCage GmbH

OTHER

Sponsor Role: collaborator

Ever Neuro Pharma GmbH

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Andreas Winkler, MD, MSc

Role: PRINCIPAL_INVESTIGATOR

Klinik Pirawarth

Locations

Klinik Pirawarth

Bad Pirawarth, , Austria

Countries

Austria

Other Identifiers

EVER-AT-0618

Identifier Type: -

Identifier Source: org_study_id