Effects of clonidine in children during electroencephalography
Phase 2
- Conditions
- Epilepsy.Epilepsy
- Registration Number
- IRCT2016102118946N5
- Lead Sponsor
- Vice Chancellor for Research, Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 45
Inclusion Criteria
age between 2 and 12 years old; history of epilepsy; history of failure to sedation with other routine medications than clonidine.
Exclusion criteria: cardiovascular disease; gastrointestinal disease; pulmonary disease; renal disease; hemodynamic instability.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Consciousness. Timepoint: Before intervention- continuously after intervention until complete consciousness. Method of measurement: Assessing by physician.
- Secondary Outcome Measures
Name Time Method Heart rate. Timepoint: Before intervention- 2 hours after intervention. Method of measurement: Assessing by physician.;Respiratory rate. Timepoint: Before intervention- 2 hours after intervention. Method of measurement: Assessing by physician.;Blood pressure. Timepoint: Before intervention- 2 hours after intervention. Method of measurement: Assessing by physician.;Body tempreture. Timepoint: Before intervention- 2 hours after intervention. Method of measurement: Assessed using thermometer.;Blood oxygen saturation. Timepoint: Before intervention- 2 hours after intervention. Method of measurement: Assessed using pulsoximetry.