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Turmeric as Treatment in Epilepsy

Samo registrirani uporabniki lahko prevajajo članke
Prijava / prijava
Povezava se shrani v odložišče
Stanje
Sponzorji
NYU Langone Health

Ključne besede

Povzetek

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.

Datumi

Nazadnje preverjeno: 03/31/2018
Prvič predloženo: 08/14/2017
Predviden vpis oddan: 08/15/2017
Prvič objavljeno: 08/17/2017
Zadnja posodobitev oddana: 04/25/2018
Zadnja posodobitev objavljena: 04/29/2018
Dejanski datum začetka študija: 02/28/2018
Predvideni datum primarnega zaključka: 10/31/2018
Predvideni datum zaključka študije: 10/31/2018

Stanje ali bolezen

Epilepsy
Dravet Syndrome
Lennox-Gastaut Syndrome
Tuberous Sclerosis
Focal Seizures

Intervencija / zdravljenje

Dietary Supplement: Turmeric Oil

Faza

-

Skupine rok

RokaIntervencija / zdravljenje
Experimental: Turmeric Oil
stable dose of orally administered turmeric oil
Dietary Supplement: Turmeric Oil
Twenty patients will be enrolled and treated with a stable dose of orally administered turmeric oil daily for 3 months.

Merila upravičenosti

Starost, primerna za študij 1 Year Za 1 Year
Spol, upravičen do študijaAll
Sprejema zdrave prostovoljceDa
Merila

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

Izid

Primarni izidni ukrepi

1. Number of epilepsy patients enrolled in study [3 months]

feasibility of recruiting patients into a prospective study designed to evaluate the effect of orally ingested turmeric oil on seizures.

Ukrepi sekundarnega rezultata

1. Number of epilepsy seizures post epilepsy treatment with turmeric [3 months]

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