An fMRI Study of Jianpi Yishen Huatan Granules for Cognitive Impairment After Acute Cerebral Infarction
NCT02752867, Not applicable, Unknown, Dongfang Hospital Beijing University of Chinese Medicine
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | An fMRI Study of Jianpi Yishen Huatan Granules for Cognitive Impairment After Acute Cerebral Infarction | ClinicalTrials.gov |
| NCT number | NCT02752867 | ClinicalTrials.gov |
| Status | Unknown | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 40 participants, estimated | ClinicalTrials.gov |
| Lead sponsor | Dongfang Hospital Beijing University of Chinese Medicine | ClinicalTrials.gov |
| Conditions | Cognitive Impairment | ClinicalTrials.gov |
| Interventions | Jianpi Yishen Huatan Granules, the placebo | ClinicalTrials.gov |
| First posted | 2016-04-27 | ClinicalTrials.gov |
| Last updated | 2019-02-26 | ClinicalTrials.gov |
Registered outcomes 19
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Changes of the fMRI outcome after the treatment | 90 days | Using the fMRI to measure the changes of neurotransmitter and brain function in the brain before and after the treatment. | ClinicalTrials.gov |
| Primary | Mini-mental state examination(MMSE) | 90 days | MMSE is an acknowledged scale to measure cognition function from the aspects of orientation ability, memory, attention, calculation ability, recall and language,etc. | ClinicalTrials.gov |
| Primary | Montreal Cognitive Assessment scale(MoCA) | 90 days | Using this scale to measure cognitive function | ClinicalTrials.gov |
| Primary | Stroop Color- Word Association Test（Stroop test） | 90 days | This is a test used to find out the memory and executive function of patients.The test contains three small test. | ClinicalTrials.gov |
| Primary | Numerical sequence test（DS-S) | 90 days | Using Numerical sequence test（DS-S) to examine memory | ClinicalTrials.gov |
| Primary | Digital color connection test (CCT) | 90 days | Using Digital color connection test (CCT) to examine executive function and attention | ClinicalTrials.gov |
| Primary | Verbal memory test(HVLT) | 90 days | Using Verbal memory test(HVLT) to examine verbal memory | ClinicalTrials.gov |
| Primary | Clinical Dementia Rating scale(CDR) | 90 days | Using Clinical Dementia Rating scale(CDR) to measure the severity of dementia | ClinicalTrials.gov |
| Secondary | National institute of health stroke scale | 90 days | Using National institute of health stroke scale to measure the severity of stroke | ClinicalTrials.gov |
| Secondary | Modified Rankin scale | 90 days | Using Modified Rankin scale to measure the recovery of neurological function | ClinicalTrials.gov |
| Secondary | Activity of Daily Living Scale | 90 days | Using this scale to measure daily living ability | ClinicalTrials.gov |
| Secondary | Scores of Chinese medicine symptoms | 90 days | Scores of Chinese medicine symptoms, which is a scale resulted from literature research, the argumentation of experts and clinical observation,contain 23 items of the core symptoms of cognitive impairment. And the scale is used to measure the changes of symptoms of Chinese medicine before and after treatment. | ClinicalTrials.gov |
| Other | whole blood cell test | 90 days | blood routine test | ClinicalTrials.gov |
| Other | routine urine test | 90 days | routine urine test | ClinicalTrials.gov |
| Other | Liver function | 90 days | test the blood to detect the liver function,such as alanine aminotransferase(ALT) ,aspartate aminotransferase(AST),total bilirubin (TBIL), γ-glutamyl transferase(γ-GT). | ClinicalTrials.gov |
| Other | electrocardiogram | 90 days | electrocardiograms are given before the experiment and on the 90th day of the experiment to test the condition of the patients' heart. | ClinicalTrials.gov |
| Other | homocysteine | 90 days | detect the homocysteine in the blood | ClinicalTrials.gov |
| Other | routine stool test | 90 days | examine stool of the patients | ClinicalTrials.gov |
| Other | kidney function | 90 days | test the blood to detect the kidney function,such as blood urea nitrogen(BUN),creatinine (CRE),Uric acid(UA) | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 1
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Stroop Color-Word Test | Primary outcome | ConductCognition |
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)