Clinical Trial to Evaluate the Efficacy and Security of Deep Brain Stimulation in Alzheimer´s Disease (ECP-EA)
Primary Purpose
Alzheimer Disease
Status
Unknown status
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
Deep brain stimulation (fornix)
Deep brain stimulation (Basal nucleus of Meynert)
Sponsored by
About this trial
This is an interventional treatment trial for Alzheimer Disease focused on measuring Deep brain stimulation, Alzheimer´s Disease, Fornix, Basal nucleus of Meynert
Eligibility Criteria
Inclusion Criteria:
- Age: Between 50-80 years old
- Diagnosis criteria of Alzheimer disease (Dubois criteria) in the previous 2 years
- Presence of tau, p-tau or Aβ in cerebrospinal fluid or positive amiloid-PET scan
- Clinical dementia rating scale (CDR): 1
- Use of cholinesterase inhibitors and/or memantine during one year at least, and worsening in neuropsychologic tests in spite of the treatment
- Informed consent (patient and caregiver or legal representative)
Exclusion Criteria:
- Brain structural disorders: primary or metastatic tumor, Hydrocephalus, stroke, brain abscess or cerebral malformation
- Vascular dementia (NINCDS-AIREN criteria)
- Neurodegenerative disease other than AD
- Psychiatric disease
- Epilepsy
- Severe or unstable comorbidity (mellitus diabetes, high blood pressure…)
Sites / Locations
- Hospital Clinico San CarlosRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Deep brain stimulation (fornix)
Deep brain stimulation (Basal nucleus of Meynert)
Arm Description
Deep brain stimulation at fornix area
Deep brain stimulation at Basal nucleus of Meynert
Outcomes
Primary Outcome Measures
Security
Determinate number of adverse event in each group such as infections, hospitalization, epilepsia, bleeding or hemiparesis
Secondary Outcome Measures
Full Information
NCT ID
NCT03290274
First Posted
September 13, 2017
Last Updated
September 19, 2017
Sponsor
Hospital San Carlos, Madrid
1. Study Identification
Unique Protocol Identification Number
NCT03290274
Brief Title
Clinical Trial to Evaluate the Efficacy and Security of Deep Brain Stimulation in Alzheimer´s Disease
Acronym
ECP-EA
Official Title
Clinical Trial to Evaluate the Efficacy and Security of Deep Brain Stimulation in Alzheimer´s Disease
Study Type
Interventional
2. Study Status
Record Verification Date
August 2017
Overall Recruitment Status
Unknown status
Study Start Date
March 1, 2017 (Actual)
Primary Completion Date
December 1, 2019 (Anticipated)
Study Completion Date
December 1, 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Hospital San Carlos, Madrid
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Approximately one million of Spaniards suffer from AlzhEimer´s Disease (AD) and this figure is expected to triple by 20150. The approved treatments modulate neurotransmission in general and are not specific or anatomically directed. In AD there is a dysfunction in cognitive and memory circuits. It has been shown that the deep brain stimulation (DBS) can specially modulate circuits in such a way that is modulable, and this approach is safe. The safety of this treatment and its biological effects are convincing enough to require further study of possible therapeutic effects of DBS in AD. The objectives are: To evaluate the security of DBS in AD (main objective). To study the influence of DBS in the progress of AD, to compare the effects of DBS on the brain metabolism neural connectivity and hubs using MEG, and to compare the effects between two different groups: fornix and Basal nucleus of Meynert (BNM). To achieve this, a prospective, double-blind comparison study between groups will be conducted, to evaluate the effects of DBS in 6 patients: group I (fornix) and group II ( BNM).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alzheimer Disease
Keywords
Deep brain stimulation, Alzheimer´s Disease, Fornix, Basal nucleus of Meynert
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
6 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Deep brain stimulation (fornix)
Arm Type
Experimental
Arm Description
Deep brain stimulation at fornix area
Arm Title
Deep brain stimulation (Basal nucleus of Meynert)
Arm Type
Experimental
Arm Description
Deep brain stimulation at Basal nucleus of Meynert
Intervention Type
Device
Intervention Name(s)
Deep brain stimulation (fornix)
Intervention Description
Deep brain stimulation at fornix
Intervention Type
Device
Intervention Name(s)
Deep brain stimulation (Basal nucleus of Meynert)
Intervention Description
Deep brain stimulation AT Basal nucleus of Meynert
Primary Outcome Measure Information:
Title
Security
Description
Determinate number of adverse event in each group such as infections, hospitalization, epilepsia, bleeding or hemiparesis
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age: Between 50-80 years old
Diagnosis criteria of Alzheimer disease (Dubois criteria) in the previous 2 years
Presence of tau, p-tau or Aβ in cerebrospinal fluid or positive amiloid-PET scan
Clinical dementia rating scale (CDR): 1
Use of cholinesterase inhibitors and/or memantine during one year at least, and worsening in neuropsychologic tests in spite of the treatment
Informed consent (patient and caregiver or legal representative)
Exclusion Criteria:
Brain structural disorders: primary or metastatic tumor, Hydrocephalus, stroke, brain abscess or cerebral malformation
Vascular dementia (NINCDS-AIREN criteria)
Neurodegenerative disease other than AD
Psychiatric disease
Epilepsy
Severe or unstable comorbidity (mellitus diabetes, high blood pressure…)
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Aurora Viloria, MD
Phone
+34913003306
Email
mariaaurora.viloria@salud.madrid.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Aurora Viloria, MD
Organizational Affiliation
Hospital Clinico San Carlos
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Clinico San Carlos
City
Madrid
Country
Spain
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Aurora Viloria, MD
Phone
+34913003306
Email
mariaaurora.viloria@salud.madrid.org
12. IPD Sharing Statement
Citations:
PubMed Identifier
35431895
Citation
Barcia JA, Viloria MA, Yubero R, Sanchez-Sanchez-Rojas L, Lopez A, Strange BA, Cabrera M, Canuet L, Gil P, Nombela C. Directional DBS of the Fornix in Alzheimer's Disease Achieves Long-Term Benefits: A Case Report. Front Aging Neurosci. 2022 Apr 1;14:809972. doi: 10.3389/fnagi.2022.809972. eCollection 2022.
Results Reference
derived
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Clinical Trial to Evaluate the Efficacy and Security of Deep Brain Stimulation in Alzheimer´s Disease
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