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Efficacy of combined extract of Nigella Sativa and Thymus Vulgaris on refractory seizures in children

Efficacy of combined extract of Nigella Sativa and Thymus Vulgaris on refractory seizures in children

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016052428043N1
Enrollment
30
Registered
2016-12-09
Start date
2016-12-10
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

epilepsy. Episodic and paroxysmal disorders

Interventions

Intervention 1: intervention group: patients with age 3-12 years receive 5cc of prepared extract(115 mg of extract is found in 5 cc of prepared drug) three times a day and patients with age >12 years
Treatment - Drugs
intervention group: patients with age 3-12 years receive 5cc of prepared extract(115 mg of extract is found in 5 cc of prepared drug) three times a day and patients with age >12 years receive 7.5 cc o
contorol group: patients with age 3-12 years receive 5cc of prepared placebo three times a day and patients with age >12 years receive 7.5 cc of prepared plasebo three times a day for two months. Then

Sponsors

Vice chancellor of Ahvaz Jundishapur University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 18 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria : children with a diagnosis of refractory seizures; having at least two episodes of seizures during one month prior to study entry; regular consumption of previous antiepileptic drugs. Exclusion criteria ; occurrence of adverse side effects such as nausea and vomiting; increase the number and duration of seizure after starting NS and TV; and dissatisfaction to continue participation in study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Seizures frequency per week. Timepoint: two months prior to study-five months during study. Method of measurement: visitable seizure scaling.;Seizure duration. Timepoint: two months prior to study-five months during study. Method of measurement: visitable seizure scaling.

Secondary

MeasureTime frame
Side effets. Timepoint: five months. Method of measurement: visitable scaling.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Heydar Azadzaeh

Ahvaz Jundishapur University of Medical Sciences

heydarazad.m@ajums.ac.ir+98 61 3374 3063

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026