Epilepsy Clinical Trial
Official title:
Turmeric as Treatment in Epilepsy
NCT number | NCT03254680 |
Other study ID # | 17-00750 |
Secondary ID | |
Status | Withdrawn |
Phase | N/A |
First received | |
Last updated | |
Start date | March 2018 |
Est. completion date | November 2018 |
Verified date | April 2018 |
Source | New York University School of Medicine |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is a single center open-label pilot clinical trial of patients 1-70 years of age with greater than 6 seizures per month diagnosed with Dravet Syndrome, Lennox-Gastaut Syndrome, Tuberous Sclerosis, or focal seizures. Twenty patients will be enrolled and treated with a stable dose of orally administered turmeric oil daily for 3 months. Patients and caregivers will be asked to keep a seizure diary logging all clinical events during the course of the study. Serum comprehensive metabolic panel, complete blood count with differential, and antiseizure medication levels, will be monitored at baseline, 1.5 months, and at the end of 3 months.
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | November 2018 |
Est. primary completion date | November 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 1 Year to 70 Years |
Eligibility |
Inclusion Criteria: - Patients with greater than greater than six seizures per month diagnosed with Dravet Syndrome, Lennox-Gastaut Syndrome, Tuberous Sclerosis, or focal seizures followed at NYU CEC. Exclusion Criteria: - Patients expected to have changes to any medications or supplements during study period - exposure to any investigational agent in the month prior to study entry - pregnant or breast feeding women, positive pregnancy test - history of non-compliance - known drug or alcohol dependence - known baseline hematologic - liver function - renal function - absorption - absorption |
Country | Name | City | State |
---|---|---|---|
United States | New York University School of Medicine | New York | New York |
Lead Sponsor | Collaborator |
---|---|
New York University School of Medicine |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of epilepsy patients enrolled in study | feasibility of recruiting patients into a prospective study designed to evaluate the effect of orally ingested turmeric oil on seizures. | 3 months | |
Secondary | Number of epilepsy seizures post epilepsy treatment with turmeric | 3 months |
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