Efficacy and Safety of Qi Zhi Tong Luo Capsule in Vascular Cognitive Impairment
Primary Purpose
Vascular Cognitive Impairment, Qi Zhi Tong Luo Capsule, Randomized Controlled Trial
Status
Completed
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
Qi Zhi Tong Luo capsule
Placebos
Sponsored by

About this trial
This is an interventional treatment trial for Vascular Cognitive Impairment
Eligibility Criteria
Inclusion Criteria:
- Decline in cognitive function from a prior baseline and impairment in at least 1 cognitive domain, the domain of cognition including executive function(Trail Making Test-part A(Chinese version,150s)>98s)), memory function decline (Hopkins verbal learning test free recall(36 points) <18.5 points), language function decline (Boston naming test (Chinese version 30 items)<22 points), and visuo-spatial functions (Clock drawing test(10 points)<8.5 points) ;
- Evidence of cerebrovascular disease relies on structural magnetic resonance imaging (MRI) , history and clinical feature. The neuroimaging should include at least one of following: a) a single large vessel infarction which was sufficient to cause cognition decline; b) infarction at a single strategic place was sufficient to cause severe cognition decline( the thalamus, angular gyrus, and basal ganglia, including the caudate nucleus and globus pallidus); c) multiple lacunar infarctions (≥3) outside the brainstem, or 2 lacunar infarcts at key locations, a single lacunar focus with extensive white matter lesions(WMLs) ; d) extensive and integrated WMLs(Fazekas scale≥3 points) ; e) intracranial hemorrhage in key parts, or ≥2 intracranial hemorrhages; f) combination of above.
- There was a clear temporal relationship between a vascular event and onset of cognitive deficit, cognitive impairment should appear within 3 months after a stroke, or abrupt deterioration, or stepwise progression of deficits; or cognitive impairment may be related to vascular factors, the Hachinski Ischemia scale (HIS) score ≥7;
- And the patients must have adequate vision and hearing to participate in study assessments;
- Have a stable caregiver;
- Can read simple articles and write simple sentences;
- Informed consent, signed informed consent by legal guardian.
Exclusion Criteria:
- Evidence of other reasons caused cognitive impairment, like Alzheimer disease, frontotemporal dementia, Parkinson disease dementia, dementia with Lewy bodies, Huntington disease, etc;
- Subdural hematoma, traffic hydrocephalus, brain tumor, thyroid disease, vitamin deficiency, or other diseases which can lead to cognitive impairment;
- Major depression (Hamilton depression rating scale [HAMD] ≥17) or other mental disorders ;
- History of drug or alcohol abuse in the past 6 month;
- History of epilepsy;
- Patients with myasthenia gravis;
- Subject cannot complete related test due to severe neurologic deficits;
- Other uncontrolled chronic illnesses, like severe cardiovascular disease (severe arrhythmia, myocardial infarction within 3 months, severe heart failure(New York Heart Association Functional Classification III and IV,); uncontrolled hypertension, diabetes);
- Severe liver or kidney dysfunction (alanine aminotransferase or aspartate transaminase was more than 1.5 times the upper limit of normal, or serum creatinine was more than the upper limit of normal);
- Concomitant use of the anticonvulsants, antipsychotics, cholinomimetic drugs, anticholinergic agents, anti-Parkinson drugs, cholinesterase inhibitors, memantine, nootropic drug, nimodipine, anticholinergic or anticholinergic antidepressant or anxiolytic and other cognition enhancers within 1 month;
- Severe asthma and chronic obstructive pulmonary disease;
- Patients with severe indigestion, gastrointestinal obstruction, gastric or duodenal ulcers;
- Patients with glaucoma;
- History of hypersensitivity to the treatment drugs;
- Participate in other clinical study.
Sites / Locations
- Dongzhimen Hospital ,Beijing University of Chinese Medicine
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Qi Zhi Tong Luo group
Placebo group
Arm Description
Patients were receiveed Qi Zhi Tong Luo Capsule 4 capsules, 2 times per day for 24 weeks. Each capsule was weighted 0.5g. Qi Zhi Tong Luo capsule (batch number: 20140805) were produced by Shanxi Zhendong Pharmaceutical Co., Ltd.
Patients were allocated to placebo, 4 capsules, 2 times per day for 24 weeks. Placebo (batch number: 20140805) were produced by Shanxi Zhendong Pharmaceutical Co., Ltd.
Outcomes
Primary Outcome Measures
Changes of Clinical Dementia Rating-Sum of the Boxes scale (CDR-SB) from baseline
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.
Changes of Mini-mental State Examination(MMSE from baseline
MMSE, 0-30 points, a lower score means severe global cognition impairment, which is used for overall endpoint assessment in clinical trials.
Secondary Outcome Measures
Changes of Hopkins Verbal Learning Test from baseline
0-48 points, higher score indicates better memory function
Changes of Clock drawing test from baseline
0-10 points, with higher scores indicating better visuo-spatial function
Changes of Ability of daily living scale from baseline
0-56 points, higher score means severe ability daily living function
Full Information
NCT ID
NCT04301466
First Posted
March 6, 2020
Last Updated
March 9, 2020
Sponsor
Dongzhimen Hospital, Beijing
Collaborators
Shanxi Zhendong Pharmacy Co., Ltd
1. Study Identification
Unique Protocol Identification Number
NCT04301466
Brief Title
Efficacy and Safety of Qi Zhi Tong Luo Capsule in Vascular Cognitive Impairment
Official Title
Efficacy and Safety of Qi Zhi Tong Luo Capsule in Vascular Cognitive Impairment: a Randomized, Double-blind, Placebo- Controlled, Multicentre Study
Study Type
Interventional
2. Study Status
Record Verification Date
March 2020
Overall Recruitment Status
Completed
Study Start Date
July 16, 2014 (Actual)
Primary Completion Date
May 30, 2018 (Actual)
Study Completion Date
May 30, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Dongzhimen Hospital, Beijing
Collaborators
Shanxi Zhendong Pharmacy Co., Ltd
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
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).
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vascular Cognitive Impairment, Qi Zhi Tong Luo Capsule, Randomized Controlled Trial
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
362 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Qi Zhi Tong Luo group
Arm Type
Experimental
Arm Description
Patients were receiveed Qi Zhi Tong Luo Capsule 4 capsules, 2 times per day for 24 weeks. Each capsule was weighted 0.5g. Qi Zhi Tong Luo capsule (batch number: 20140805) were produced by Shanxi Zhendong Pharmaceutical Co., Ltd.
Arm Title
Placebo group
Arm Type
Placebo Comparator
Arm Description
Patients were allocated to placebo, 4 capsules, 2 times per day for 24 weeks. Placebo (batch number: 20140805) were produced by Shanxi Zhendong Pharmaceutical Co., Ltd.
Intervention Type
Drug
Intervention Name(s)
Qi Zhi Tong Luo capsule
Intervention Description
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.
Intervention Type
Drug
Intervention Name(s)
Placebos
Intervention Description
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.
Primary Outcome Measure Information:
Title
Changes of Clinical Dementia Rating-Sum of the Boxes scale (CDR-SB) from baseline
Description
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
Title
Changes of Mini-mental State Examination(MMSE from baseline
Description
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
Secondary Outcome Measure Information:
Title
Changes of Hopkins Verbal Learning Test from baseline
Description
0-48 points, higher score indicates better memory function
Time Frame
week 0, 12, 24,36
Title
Changes of Clock drawing test from baseline
Description
0-10 points, with higher scores indicating better visuo-spatial function
Time Frame
week 0, 12, 24,36
Title
Changes of Ability of daily living scale from baseline
Description
0-56 points, higher score means severe ability daily living function
Time Frame
week 0, 12, 24,36
10. Eligibility
Sex
All
Minimum Age & Unit of Time
45 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Decline in cognitive function from a prior baseline and impairment in at least 1 cognitive domain, the domain of cognition including executive function(Trail Making Test-part A(Chinese version,150s)>98s)), memory function decline (Hopkins verbal learning test free recall(36 points) <18.5 points), language function decline (Boston naming test (Chinese version 30 items)<22 points), and visuo-spatial functions (Clock drawing test(10 points)<8.5 points) ;
Evidence of cerebrovascular disease relies on structural magnetic resonance imaging (MRI) , history and clinical feature. The neuroimaging should include at least one of following: a) a single large vessel infarction which was sufficient to cause cognition decline; b) infarction at a single strategic place was sufficient to cause severe cognition decline( the thalamus, angular gyrus, and basal ganglia, including the caudate nucleus and globus pallidus); c) multiple lacunar infarctions (≥3) outside the brainstem, or 2 lacunar infarcts at key locations, a single lacunar focus with extensive white matter lesions(WMLs) ; d) extensive and integrated WMLs(Fazekas scale≥3 points) ; e) intracranial hemorrhage in key parts, or ≥2 intracranial hemorrhages; f) combination of above.
There was a clear temporal relationship between a vascular event and onset of cognitive deficit, cognitive impairment should appear within 3 months after a stroke, or abrupt deterioration, or stepwise progression of deficits; or cognitive impairment may be related to vascular factors, the Hachinski Ischemia scale (HIS) score ≥7;
And the patients must have adequate vision and hearing to participate in study assessments;
Have a stable caregiver;
Can read simple articles and write simple sentences;
Informed consent, signed informed consent by legal guardian.
Exclusion Criteria:
Evidence of other reasons caused cognitive impairment, like Alzheimer disease, frontotemporal dementia, Parkinson disease dementia, dementia with Lewy bodies, Huntington disease, etc;
Subdural hematoma, traffic hydrocephalus, brain tumor, thyroid disease, vitamin deficiency, or other diseases which can lead to cognitive impairment;
Major depression (Hamilton depression rating scale [HAMD] ≥17) or other mental disorders ;
History of drug or alcohol abuse in the past 6 month;
History of epilepsy;
Patients with myasthenia gravis;
Subject cannot complete related test due to severe neurologic deficits;
Other uncontrolled chronic illnesses, like severe cardiovascular disease (severe arrhythmia, myocardial infarction within 3 months, severe heart failure(New York Heart Association Functional Classification III and IV,); uncontrolled hypertension, diabetes);
Severe liver or kidney dysfunction (alanine aminotransferase or aspartate transaminase was more than 1.5 times the upper limit of normal, or serum creatinine was more than the upper limit of normal);
Concomitant use of the anticonvulsants, antipsychotics, cholinomimetic drugs, anticholinergic agents, anti-Parkinson drugs, cholinesterase inhibitors, memantine, nootropic drug, nimodipine, anticholinergic or anticholinergic antidepressant or anxiolytic and other cognition enhancers within 1 month;
Severe asthma and chronic obstructive pulmonary disease;
Patients with severe indigestion, gastrointestinal obstruction, gastric or duodenal ulcers;
Patients with glaucoma;
History of hypersensitivity to the treatment drugs;
Participate in other clinical study.
Facility Information:
Facility Name
Dongzhimen Hospital ,Beijing University of Chinese Medicine
City
Beijing
State/Province
Beijing
ZIP/Postal Code
100700
Country
China
12. IPD Sharing Statement
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Efficacy and Safety of Qi Zhi Tong Luo Capsule in Vascular Cognitive Impairment
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