NEURoaid II (MLC 901) Assessment in Cognitively Impaired Not Demented Subjects
NCT ID: NCT01847924
Last Updated: 2018-07-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE2
103 participants
INTERVENTIONAL
2013-03-31
2018-04-30
Brief Summary
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Neuroaid is a Traditional Chinese Medicine which has been shown to stimulate growth of brain cells and connections in animals. Neuroaid may improve blood flow in the brain and functional recovery after stroke in patients. Neuroaid-II is a simplified formula with only the main 9 herbal ingredients of the original formula and no animal ingredients.
The NEURoaid II (MLC 901) assessment in cognitively Impaired not demented subjects: a pilot double blind, placebo-controlled randomized Trial on Efficacy and Safety (NEURITES) Study is a 24-week, early phase trial of Neuroaid-II in patients who have thinking problems after stroke. The study aims to investigate the effectiveness of the study drug in improving cognitive performance. The safety of the study drug will be closely monitored using adverse events, laboratory tests and vital signs.
The trial is important as it aims to set new standards for the scientific evaluation of Asian Traditional Medicine for integration into standard medicine practice. It may potentially establish a novel therapeutic approach for improving cognition after stroke.
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Detailed Description
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Neuroaid is a Traditional Chinese Medicine which has been shown to induce neurogenesis, promote cell proliferation and stimulate development of axonal and dendritic networks in animal models. Neuroaid may improve functional recovery after stroke in patients. Neuroaid-II is a simplified formulation with only 9 herbal and no animal ingredients.
The NEURoaid II (MLC 901) assessment in cognitively Impaired not demented subjects: a pilot double blind, placebo-controlled randomized Trial on Efficacy and Safety (NEURITES) Study is a 24-week Phase II study. The primary outcome is executive function as measured by the Verbal Fluency test. Secondary outcomes include cognitive measures such as the ADAS-Cog, MoCA, MMSE and a Cognitive Battery; Activities of Daily Living as measured by the ADCS-ADL scale; behaviour as measured by the Neuropsychiatric Inventory and depression as measured by the Geriatric Depression Scale and Beck Depression Scale. Safety and tolerability will be assessed using adverse events, laboratory tests, and vital signs.
The trial is important for translational medicine in Singapore through setting new standards for systematic evaluation of Traditional Medicine for integration into standard medicine practice
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
QUADRUPLE
Study Groups
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MLC901
Brand: Neuroaid II. Dosage: 2 capsules 3 times a a day
MLC901
24 weeks intervention with orally MLC901. 2 capsules 3 times a day
placebo
MLC901 matching placebo made by the same manufacturer for this study dosage: 2 capsules 3 times a day.
Placebo
24 weeks intervention with orally placebo. 2 capsules 3 times a day
Interventions
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MLC901
24 weeks intervention with orally MLC901. 2 capsules 3 times a day
Placebo
24 weeks intervention with orally placebo. 2 capsules 3 times a day
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Aged 55 to 85, living with a caregiver,
3. Modified Rankin score \<=3.
4. Diagnosis of CIND due to cerebrovascular disease.
5. Cognitive impairment documented by neuropsychological evaluation within 12 months of index stroke/TIA. Not demented by DSM-IV criteria
6. Written informed consent by subject
Exclusion Criteria
2. DSM IV current diagnosis of dementia or major depression (patients may be included if currently being treated on an antidepressant and stabilized after 3 months).
3. A disability that may prevent the subject from completing all study requirements (e.g. blindness, deafness, severe language difficulty).
4. Ingestion of any of the following : an investigational drug in the past four weeks, a drug or treatment known to cause major organ system toxicity during the past four weeks, acetylcholinesterase inhibitors or memantine in the past 3 months
55 Years
85 Years
ALL
No
Sponsors
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National University Hospital, Singapore
OTHER
Responsible Party
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Principal Investigators
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Christopher LH Chen, FRCP
Role: PRINCIPAL_INVESTIGATOR
National University Hospital, Singapore
Locations
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University of Santo Tomas Hospital
Manila, National Capital Region, Philippines
National University Hospital
Singapore, , Singapore
Singapore General Hospital
Singapore, , Singapore
National Neuroscience Institute
Singapore, , Singapore
National Geriatric Hospital
Hanoi, , Vietnam
Countries
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Other Identifiers
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MLC901-1
Identifier Type: -
Identifier Source: org_study_id
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