Dongzhimen Hospital ,Beijing University of Chinese Medicine
Beijing, Beijing Municipality, 100700, China
NCT Number: NCT04301466
Qi Zhi Tong Luo (QZTL) capsule, a traditional Chinese herbal medicine, which was used to treat stoke-related symptoms, include trouble speaking, paralysis and trouble walking. This study aimed to evaluate the efficacy and safety of QZTL capsule in the treatment of vascular cognitive impairment. This study was designed as randomized, double-blind, parallel, placebo-controlled, multicentre trial. It consisted of a single-blind run-in period using placebo only (2 weeks) and a double-blind treatment phase after randomization (24 weeks), and follow-up 12 weeks after withdrawal.The primary efficacy variables included changes from baseline in the Clinical Dementia Rating scale-Sum Box (CDR-SB) and the Mini-mental State Examination (MMSE) after 24 weeks of treatment. The secondary efficacy measurements include the Clock Drawing Test (CDT), Hopkins Verbal Learning Test (HVLT) and Ability of Daily Living (ADL).
Looking for future studies?
Notify Me45 year–80 year
All sexes
Interventional
Phase 2 / Phase 3
Beijing, Beijing Municipality, 100700, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients were receiveed Qi Zhi Tong Luo Capsule 4 capsules, 2 times per day for 24 weeks. QZTL capsule, a traditional Chinese medicine. Each capsule was weighted 0.5g.
Patients were allocated to placebo, 4 capsules, 2 times per day for 24 weeks.To preserve blinding, the placebo had an identical taste and appearance to the experimental drugs. Placebo (batch number: 20140805) were produced by Shanxi Zhendong Pharmaceutical Co., Ltd.
Time frame: week 0, 12, 24,36
CDR-SB is a standard for disease grading in clinical studies of dementia and is used for overall endpoint assessment in clinical trials. The CDR-SB scores from 0-18 points, and a higher score indicates higher impairment.
Time frame: week 0, 12, 24,36
MMSE, 0-30 points, a lower score means severe global cognition impairment, which is used for overall endpoint assessment in clinical trials.
Time frame: week 0, 12, 24,36
0-48 points, higher score indicates better memory function
Time frame: week 0, 12, 24,36
0-10 points, with higher scores indicating better visuo-spatial function
Time frame: week 0, 12, 24,36
0-56 points, higher score means severe ability daily living function
Dongzhimen Hospital, Beijing
Other
Efficacy and Safety of Qi Zhi Tong Luo Capsule in Vascular Cognitive Impairment: a Randomized, Double-blind, Placebo- Controlled, Multicentre Study
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT02669394
Arterial Occlusive Diseases, Arteriosclerosis
Vancouver, British Columbia, Canada
View Trial DetailsNCT04769310
Arrhythmias, Cardiac, Atrial Fibrillation
New Orleans, Louisiana, United States
View Trial DetailsNCT05524181
Alzheimer Disease, Arterial Occlusive Diseases
Philadelphia, Pennsylvania, United States
View Trial DetailsNCT02330510
Alzheimer Disease, Alzheimer's Disease
Calgary, Alberta, Canada
View Trial Details