Skip to content

Effects of clonidine in children during electroencephalography

Clonidine sedation effects in children during electroencephalography

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016102118946N5
Enrollment
45
Registered
2016-11-11
Start date
2015-12-31
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. Epilepsy

Interventions

0.05-0.2 mg of clonidine will be administered to patients orally based on their weight (for 30 kg 0.15 to 0.2 mg of clonidine)..
Treatment - Drugs
0.05-0.2 mg of clonidine will be administered to patients orally based on their weight (for 30 kg 0.15 to 0.2 mg of clonidine).

Sponsors

Vice Chancellor for Research, Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 12 Years

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Consciousness. Timepoint: Before intervention- continuously after intervention until complete consciousness. Method of measurement: Assessing by physician.

Secondary

MeasureTime frame
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.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr. Masoumeh Ghasempour Alamdari

Clinical Educational Center of Children, Tabriz University of Medical Sciences

rzanz@yahoo.com+98 41 3523 1827

Outcome results

None listed

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