Clinical TrialID 6911
The Safety and Tolerability of Kinetin, in Patients With Familial Dysautonomia
NCT02274051
Familial Dysautonomia
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 6911
- Evidence Id
- 6911
- Core Evidence Id
- 6911
- Source Clinical Trial Id
- 6903
- Herb2 Clinical Trial Id
- HBCT006903
- Nct Id
- NCT02274051
- Title
- The Safety and Tolerability of Kinetin, in Patients With Familial Dysautonomia
- Status
- Completed
- Phase
- Phase 1
- Study Result
- No
- Study Condition
- Familial Dysautonomia
- Study Type
- Interventional
- Study Design
- Allocation: NA|Intervention Model: SINGLE_GROUP|Masking: NONE|Primary Purpose: TREATMENT
- Intervention
- DIETARY_SUPPLEMENT: Kinetin
- Intervention Allocation
- Intervention Model
- Single_Group
- Intervention Mask
- Intervention Purpose
- Treatment
- Gender
- All
- Age
- Child, Adult, Older_Adult
- Enrollment
- 15
- Outcome Measure
- Change in Safety blood labs, safety blood labs (CBC, metabolic panel), At baseline and after each 6 months period and at 36 months|Change in vital signs, Sitting and standing blood pressure measurements and heart rate, At baseline and after each 6 months period and at 36 months|Change in ECG, 12 lead ECG measures, At baseline and after each 6 months period and at 36 months|Number of participants with adverse events, Number of adverse events, At baseline and after each 6 months period and at 36 months
- Sponsor Collaborator
- NYU Langone Health
- Funded By
- OTHER
- Location
- NYU Langone Medical Center, New York, New York, 10016, United States
- Other Id
- 09-0762
- Start Date
- 2009-11
- Primary Completion Date
- 2019-05-04
- Completion Date
- 2019-05-04
- First Posted
- 2014-10-24
- Results First Posted
- Last Update Posted
- 2019-06-18
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT02274051
- Title Cn
- Title En
- The Safety and Tolerability of Kinetin, in Patients With Familial Dysautonomia
- Bilingual Status
- semi_complete