Status:
COMPLETED
ATP in Alzheimer Disease
Lead Sponsor:
Sara Varea
Conditions:
Alzheimer's Disease
Eligibility:
All Genders
55-85 years
Phase:
PHASE2
Brief Summary
To Check whether systemic treatment with ATP alters the profile of cerebral metabolism in patients with Alzheimer's disease using MRS techniques (Magnetic Resonance Spectroscopy) and adjust the infusi...
Eligibility Criteria
Inclusion
- 1\. Men and women aged 55-85 years
- 2\. Diagnosis of possible or probable Alzheimer disease according to NIA-AA 2011 criteria.
- 3\. Global Deterioration Scale Stadium 5-6 / 15-5 Mini-mental State examination
- 4\. The patient is living with a family as a primary caregiver or a caregiver trained to accompany adequate and all intervention and follow-up visits. Patient and caregiver knowledge of local languages sufficient.
- 5\. The patient and caregiver willing to participate in the study. There is a high probability that patient and caregiver to complete the study.
- 6\. The patient has no sensory deficits preventing evaluation.
- 7\. The patient receives a stable Alzheimer Disease conventional medication. No change in treatment at least 90 days prior to selection.
- 8\. The patient receives a conventional stable medication for possible comorbidities. No change in treatment at least 90 days prior to selection.
- 9\. The subject or his legal representative give prior informed consent that includes genetic studies of Apolipoprotein E and rs11870474.
Exclusion
- 1\. Concomitant severe neurological disease Alzheimer Disease.
- 2\. Presence or history of psychiatric disorders with an emphasis on positive behavioral disorders associated with Alzheimer Disease (aggressiveness, agitation, delusions, hallucinations, anxiety).
- 3\. Current Severe systemic disease that may prevent completion of the study.
- 4\. History STROKE.
- 5\. History of convulsions and use of anticonvulsants.
- 6\. History of myocardial infarction, angina pectoris, cardiac arrhythmias and other serious cardiovascular disorders such as congestive heart failure, and valvular aneurysms.
- 7\. Background Diabetes mellitus and / or pictures of hypoglycemia.
- 8\. Uncontrolled hypertension (systolic\> 160 mmHg and / or Diastolic\> 95 mmHg).
- 9\. Systemic hypotension (SBP \<86 mmHg) or bradycardia (\<50 beats per minute)
- 10\. Bronchial Asthma History or lung diseases that cause bronchospasm or bronchoconstriction
- 11\. Kidney failure (patients with medical restrictions or income parenteral intake of fluids).
- 12\. Liver failure.
- 13\. Respiratory failure (need supplemental oxygen supply)
- 14\. Blood donation in the last 90 days or anemia (Hb \<10g/dL)
- 15\. Use connection (\<30 days prior to screening) of antidepressants, sedatives and hypnotics.
- 16\. Using Alzheimer Disease experimental drugs in the last 60 days prior to screening.
- 17\. Women who are pregnant or fertile
- 18\. Inadequate venous access to prevent parenteral administration of infusions.
Key Trial Info
Start Date :
December 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 1 2016
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT02279511
Start Date
December 1 2014
End Date
February 1 2016
Last Update
March 29 2017
Active Locations (2)
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1
Fundació ACE
Barcelona, Barcelona, Spain, 08028
2
Hospital Sanitas CIMA
Barcelona, Spain