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UnknownNCT04346862

Evaluation the Effect of Acetyl-L-carnitine in Patients With Mild Cognitive Impairment Accompanied With Chronic Cerebrovascular Disease

Phase IV Study to Evaluate the Effect of Improvement in Cognitive Impairment of Acetyl-L-carnitine in Patients With Mild Cognitive Impairment Accompanied With Chronic Cerebrovascular Disease

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
636 (estimated)
Sponsor
Hanmi Pharmaceutical Company Limited · Industry
Sex
All
Age
55 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the efficacy of Acetyl-L-carnitine in patient with Mild Cognitive Impairment associated with chronic cerebrovascular disease.

Conditions

Interventions

TypeNameDescription
DRUGAcetyl-L-carnitine hydrochloride 500mgThe participants will receive treatment of Acetyl-L-carnitine hydrochloride 500mg, orally, 3 times a day for 24weeks
DRUGPlaceboThe participants will receive treatment of placebo of Acetyl-L-carnitine hydrochloride 500mg, orally, 3 times a day for 24weeks

Timeline

Start date
2016-01-26
Primary completion
2020-06-30
Completion
2020-06-30
First posted
2020-04-15
Last updated
2020-04-21

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT04346862. Inclusion in this directory is not an endorsement.

Evaluation the Effect of Acetyl-L-carnitine in Patients With Mild Cognitive Impairment Accompanied With Chronic Cerebrov (NCT04346862) · Clinical Trials Directory