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Cognitive Rehabilitation and Galantamine for Post Stroke Cognitive Impairment (COGICRehab)

Primary Purpose

Stroke, Cognitive Impairment

Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Galantamine
placebo
Sponsored by
Institut National de la Santé Et de la Recherche Médicale, France
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Stroke focused on measuring modification of fMRI maps after galantamine/placebo

Eligibility Criteria

35 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Written consent form signed by the patient,
  • Patient must be affiliated with a social security system,
  • Age: 35-70,
  • First symptomatic stroke,
  • Brain ischemic lesion on MRI DWI consistent with a recent ischemic stroke,
  • Absence of cognitive decline before the stroke,
  • Detailed cognitive complaint of patient or the environment,
  • Patients with a cognitive impairment (VCI-ND criteria: impairment in at least one cognitive domain with a score below 2 standard deviation according to clinical norms in at least two cognitive functions exploring this domain. VCI-ND was diagnosed in the absence of dementia according to the DSM IV,
  • Absence of hospitalization for cardiovascular disease from the acute phase of the qualifying event,
  • NIHSS < 6,
  • mRs < 4,
  • Absence of aphasia, apraxia and neglect severe,
  • Patients not previously treated with cholinesterase inhibitors or memantine centrally acting regardless of the duration of treatment and date of prescription,
  • Visual skills, auditory and oral or written expression sufficient to achieve adequate neuropsychological tests,
  • Women of childbearing potential must be using contraception and a pregnancy test will be conducted at the screening visit.

Exclusion Criteria:

  • Subjects with contraindication to MRI (a pacemaker or a defibrillator, an implanted material activated by an electrical, magnetic or mechanical carriers of hemostatic clips of intracerebral aneurysms or carotid arteries, bearing orthopedic implants, claustrophobia),
  • Preexisting cognitive decline,
  • VCI-ND criteria not fulfilled,
  • Patients previously treated with cholinesterase inhibitors or memantine centrally acting regardless of the duration of treatment and date of prescription,
  • Known allergy or intolerance to cholinesterase inhibitors or their excipients,
  • Depression,
  • General Health scalable,
  • Progressive neurological disease causing cognitive impairment,
  • Clinically significant endocrine disease,
  • Patients with urinary retention or who have recently had surgery at the bladder,
  • Patients with rare hereditary problems of fructose intolerance, malabsorption of glucose and galactose or sucrase-isomaltase insufficiency should not take this medicine,
  • Patient with severe hepatic impairment,
  • Patient with severe renal impairment,
  • Patients with both hepatic and renal significant,
  • Patients with sick sinus disorder or other supraventricular cardiac conduction or in those receiving concomitant drugs significantly slowing heart rate, such as digoxin and beta blockers or in patients with uncorrected electrolyte disorders,
  • Period immediately post-myocardial infarction, recent-onset atrial fibrillation, bundle branch block second degree or higher degree, unstable angina or congestive heart failure, especially NYHA group III-IV,
  • Patients with gastrointestinal obstruction or recent surgery in gastrointestinal,
  • Patients receiving other cholinomimetic agents (such as ambenonium, donepezil, neostigmine, pyridostigmine, rivastigmine and pilocarpine) administered systemically,
  • Breast feeding women,
  • Alcohol abuse,
  • Substance abuse,
  • Psychiatric condition scalable,
  • Patients who will have surgery during the study participation,
  • Known or suspected pregnancy, confirmed by a urine pregnancy test. This test will be done prior to randomization if a woman of childbearing age without oral contraception is included in the study, if a pregnancy is declared during the participation in the study, the blind will be removed and the patient will be directed towards a specialist,
  • Patient can not stop all treatment prohibited for this project at least 2 months before inclusion,
  • French language level insufficient to properly participate in neuropsychological assessment,
  • Transient ischemic stroke,
  • Subarachnoid hemorrhage or intraparenchymal,
  • Patient under protection of law or under another protection.

Sites / Locations

  • Service de Neurologie, CHU Toulouse Purpan

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Galantamine

placebo

Arm Description

16mg galantamine progressively

placebo

Outcomes

Primary Outcome Measures

fMRI
Comparison between the two groups on fMRI map activation with a N-back task at week 20

Secondary Outcome Measures

Full Information

First Posted
July 1, 2011
Last Updated
August 26, 2021
Sponsor
Institut National de la Santé Et de la Recherche Médicale, France
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1. Study Identification

Unique Protocol Identification Number
NCT01508494
Brief Title
Cognitive Rehabilitation and Galantamine for Post Stroke Cognitive Impairment
Acronym
COGICRehab
Official Title
Evaluation de l'efficacité de la Galantamine Versus Placebo associée à Une Revalidation Neuropsychologique Chez Des Patients présentant un Trouble Cognitif après un Premier Infarctus cérébral : étude en Neuroimagerie Fonctionnelle
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Completed
Study Start Date
June 29, 2011 (Actual)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
June 22, 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Institut National de la Santé Et de la Recherche Médicale, France

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The investigators would like to conduct a double blind placebo-controlled prospective study to show the impact of a treatment combining a specific cognitive rehabilitation program and acetylcholinesterase inhibitors on executive function of young patients 3 months after a first symptomatic stroke. The secondary objectives will be to assess cognitive changes performance (executive but also non trained functions such as memory) before and after treatments and treatment effect on activity of daily living and on quality of life. The main objective of this study is to show the impact of this combined treatment on brain activation maps in VCI-ND patients in the post-acute phase (3 months) after a stroke. Treatment effect will be assessed by functional MRI (fMRI) while patients will be performing a specific executive task. The investigators hypothesize that the specific rehabilitation associated with acetylcholinestrase inhibitors treatment will focalize cerebral activation observed in fMRI, improve executive functions specifically, improve non trained cognitive functions (generalization effect).
Detailed Description
Recent studies, including the investigators', have shown that neuropsychological alteration is frequent and underestimated after stroke (Vascular Cognitive Impairment (VCI). VCI-No Dementia (VCI-ND) is characterized by a mild cognitive alteration in relation to a cerebrovascular lesion, diagnosed by a neuropsychological assessment, and without major alteration in the activities of daily living, but that can represent an issue in return to work for young patients. Some studies demonstrated that cognitive rehabilitation or pharmacological intervention may to improve patients' cognition and social functioning. The investigators hypothesize that a combination of pharmacological and cognitive rehabilitation treatments is beneficial on executive but also other cognitive function in VCI-ND patients Therefore the investigators would like to conduct a double blind placebo-controlled prospective study to show the impact of a treatment combining a specific cognitive rehabilitation program and acetylcholinesterase inhibitors on executive function of young patients 3 months after a first symptomatic stroke. The secondary objectives will be to assess cognitive changes performance (executive but also non trained functions such as memory) before and after treatments and treatment effect on activity of daily living and on quality of life. The main objective of this study is to show the impact of this combined treatment on brain activation maps in VCI-ND patients in the post-acute phase (3 months) after a stroke. Treatment effect will be assessed by functional MRI (fMRI) while patients will be performing a specific executive task. The investigators hypothesize that the specific rehabilitation associated with acetylcholinestrase inhibitors treatment will focalize cerebral activation observed in fMRI, improve executive functions specifically, improve non trained cognitive functions (generalization effect).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Cognitive Impairment
Keywords
modification of fMRI maps after galantamine/placebo

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
47 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Galantamine
Arm Type
Active Comparator
Arm Description
16mg galantamine progressively
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
placebo
Intervention Type
Drug
Intervention Name(s)
Galantamine
Intervention Description
16 mg galantamine daily P/O
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
placebo
Primary Outcome Measure Information:
Title
fMRI
Description
Comparison between the two groups on fMRI map activation with a N-back task at week 20
Time Frame
week 20

10. Eligibility

Sex
All
Minimum Age & Unit of Time
35 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Written consent form signed by the patient, Patient must be affiliated with a social security system, Age: 35-70, First symptomatic stroke, Brain ischemic lesion on MRI DWI consistent with a recent ischemic stroke, Absence of cognitive decline before the stroke, Detailed cognitive complaint of patient or the environment, Patients with a cognitive impairment (VCI-ND criteria: impairment in at least one cognitive domain with a score below 2 standard deviation according to clinical norms in at least two cognitive functions exploring this domain. VCI-ND was diagnosed in the absence of dementia according to the DSM IV, Absence of hospitalization for cardiovascular disease from the acute phase of the qualifying event, NIHSS < 6, mRs < 4, Absence of aphasia, apraxia and neglect severe, Patients not previously treated with cholinesterase inhibitors or memantine centrally acting regardless of the duration of treatment and date of prescription, Visual skills, auditory and oral or written expression sufficient to achieve adequate neuropsychological tests, Women of childbearing potential must be using contraception and a pregnancy test will be conducted at the screening visit. Exclusion Criteria: Subjects with contraindication to MRI (a pacemaker or a defibrillator, an implanted material activated by an electrical, magnetic or mechanical carriers of hemostatic clips of intracerebral aneurysms or carotid arteries, bearing orthopedic implants, claustrophobia), Preexisting cognitive decline, VCI-ND criteria not fulfilled, Patients previously treated with cholinesterase inhibitors or memantine centrally acting regardless of the duration of treatment and date of prescription, Known allergy or intolerance to cholinesterase inhibitors or their excipients, Depression, General Health scalable, Progressive neurological disease causing cognitive impairment, Clinically significant endocrine disease, Patients with urinary retention or who have recently had surgery at the bladder, Patients with rare hereditary problems of fructose intolerance, malabsorption of glucose and galactose or sucrase-isomaltase insufficiency should not take this medicine, Patient with severe hepatic impairment, Patient with severe renal impairment, Patients with both hepatic and renal significant, Patients with sick sinus disorder or other supraventricular cardiac conduction or in those receiving concomitant drugs significantly slowing heart rate, such as digoxin and beta blockers or in patients with uncorrected electrolyte disorders, Period immediately post-myocardial infarction, recent-onset atrial fibrillation, bundle branch block second degree or higher degree, unstable angina or congestive heart failure, especially NYHA group III-IV, Patients with gastrointestinal obstruction or recent surgery in gastrointestinal, Patients receiving other cholinomimetic agents (such as ambenonium, donepezil, neostigmine, pyridostigmine, rivastigmine and pilocarpine) administered systemically, Breast feeding women, Alcohol abuse, Substance abuse, Psychiatric condition scalable, Patients who will have surgery during the study participation, Known or suspected pregnancy, confirmed by a urine pregnancy test. This test will be done prior to randomization if a woman of childbearing age without oral contraception is included in the study, if a pregnancy is declared during the participation in the study, the blind will be removed and the patient will be directed towards a specialist, Patient can not stop all treatment prohibited for this project at least 2 months before inclusion, French language level insufficient to properly participate in neuropsychological assessment, Transient ischemic stroke, Subarachnoid hemorrhage or intraparenchymal, Patient under protection of law or under another protection.
Facility Information:
Facility Name
Service de Neurologie, CHU Toulouse Purpan
City
Toulouse
ZIP/Postal Code
31059
Country
France

12. IPD Sharing Statement

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Cognitive Rehabilitation and Galantamine for Post Stroke Cognitive Impairment

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