EGb 761 in the Syndrome of MCI With Concomitant CVD
Recruiting
Phase 2Interventional Study
Mild Cognitive ImpairmentCerebrovascular Disease
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
Prior Safety Data
This treatment has already been tested in at least one earlier human trial.
Ready to participate?
Review the details below, then apply to join this clinical trial.
At a Glance
Age
45 – 85
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
134 (estimated)
Sponsor
National Neuroscience Institute · Other
Who this trial is looking for
This trial is looking for adults aged 45 to 85 with mild cognitive impairment and cerebrovascular disease. Participants will receive the treatment EGb 761 and help researchers understand its effects on cognition and safety.
Are You a Good Fit for This Trial?
Must not be takingAntidepressantsAntipsychoticsBenzodiazepinesAcetylcholinesterase inhibitorsNMDA antagonists
You may be able to join if
I have been diagnosed with mild cognitive impairment.
I have a Global Clinical Dementia Rating Score of 0.5.
I am between 45 and 85 years old.
I can read and understand the study requirements.
I have cerebrovascular disease shown by brain imaging.
I have given written consent to participate.
You may not be able to join if
I am currently taking antidepressants.
I am currently taking antipsychotics.
I am currently taking benzodiazepines.
I am currently taking acetylcholinesterase inhibitors.
I am currently taking NMDA antagonists.
I have a medical condition that prevents me from taking EGb 761.
Summarized in plain language from this trial's official eligibility criteria.
The full criteria are further down this page — only the research team can
confirm whether you qualify.
Think this trial could be right for you?
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EGb 761 has been demonstrated to be useful in improving cognitive and global clinical outcomes in patients with cognitive impairment or dementia, when administered at a daily dosage of 240mg in randomised controlled trials through several neuroprotective mechanisms of action. The study aims to determine the efficacy and safety profile of EGb 761 as a prescribed clinical drug for patients with MCI …
EGb 761 has been demonstrated to be useful in improving cognitive and global clinical outcomes in patients with cognitive impairment or dementia, when administered at a daily dosage of 240mg in randomised controlled trials through several neuroprotective mechanisms of action. The study aims to determine the efficacy and safety profile of EGb 761 as a prescribed clinical drug for patients with MCI + CVD.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Patients who have been diagnosed with MCI based on the Petersen criteria and Albert MS criteria
* Patients who have a Global Clinical Dementia Rating Score of 0.5
* Patients aged 45 to 85 years at study entry
* Patients who are literate and able to complete the cognitive evalu…
Inclusion Criteria:
* Patients who have been diagnosed with MCI based on the Petersen criteria and Albert MS criteria
* Patients who have a Global Clinical Dementia Rating Score of 0.5
* Patients aged 45 to 85 years at study entry
* Patients who are literate and able to complete the cognitive evaluations in the opinion of the investigators
* Patients with the presence of CVD, defined as the presence of white matter hyperintensities (WMH) of Fazekas grade 2 or 3 on MRI brain imaging (done up to 12 months prior to recruitment) or CT scans for patients contraindicated from MRI scans
* Patients who provide written informed consent to participate in the study
Exclusion Criteria:
* Participants should not be receiving antidepressants, antipsychotics, benzodiazepines, acetylcholinesterase inhibitors or NMDA antagonists during the study. Additionally, contraindications for EGb 761 as given in the local prescribing information/Summary of Product Characteristics (SmPC) should be observed.
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