Clinical TrialID 305
Use of Gou-Teng to Treat Patients With Mild Cognitive Impairment
NCT04532697
Mild Cognitive Impairment|White Matter Hyperintensity
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 305
- Evidence Id
- 305
- Core Evidence Id
- 305
- Source Clinical Trial Id
- 291
- Herb2 Clinical Trial Id
- HBCT000291
- Nct Id
- NCT04532697
- Title
- Use of Gou-Teng to Treat Patients With Mild Cognitive Impairment
- Status
- Phase
- Study Result
- No
- Study Condition
- Mild Cognitive Impairment|White Matter Hyperintensity
- Study Type
- Interventional
- Study Design
- Allocation: RANDOMIZED|Intervention Model: PARALLEL|Masking: QUADRUPLE (PARTICIPANT, CARE_PROVIDER, INVESTIGATOR, OUTCOMES_ASSESSOR)|Primary Purpose: TREATMENT
- Intervention
- OTHER: Uncaria Rhynchophylla (Gou-Teng)|OTHER: Placebo
- Intervention Allocation
- Randomized
- Intervention Model
- Parallel
- Intervention Mask
- Quadruple
- Intervention Purpose
- Treatment
- Gender
- All
- Age
- Older_Adult
- Enrollment
- 56
- Outcome Measure
- HK-MoCA, The Montreal Cognitive Assessment (MoCA) was designed as a rapid screening instrument for mild cognitive dysfunction. Scoring of HK MoCA ranges from 0 to 30 points. 3 cutoff percentile will be used: 2nd, 7th, and 16th percentile. The cut-off percentile at 16th above is considered normal and it shows worse with the decreasing percentile., 16 weeks
- Sponsor Collaborator
- Chinese University of Hong Kong
- Funded By
- OTHER
- Location
- The Chinese University of Hong Kong, Hong Kong, Hong Kong
- Other Id
- MCI-Gou Teng study
- Start Date
- 2020-11-24
- Primary Completion Date
- 2022-03-31
- Completion Date
- 2022-09-30
- First Posted
- 2020-08-31
- Results First Posted
- Last Update Posted
- 2021-08-04
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT04532697
- Title Cn
- Title En
- Use of Gou-Teng to Treat Patients With Mild Cognitive Impairment
- Bilingual Status
- semi_complete