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Study of Effects of Isofeloran and Sevofeloran in Agitation

Comparison Isofeloran vs Sevofeloran in balance explosion Agitated in Recovery Children under Anesthesia,Respect of Action on Urology

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190308042970N1
Enrollment
100
Registered
2019-07-26
Start date
2019-06-22
Completion date
Unknown
Last updated
2019-10-07

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

Conditions

Agitation occurs in children undergoing urinary anesthesia.

Interventions

Intervention 1: Intervention group:Isoflurane An anesthetic anesthetic is used to induce anesthetic anesthetics. In the room, it is liquid and in the form of a 100cc inhaler.

Sponsors

Sabzevar University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1- Children between 1 to 12 years. 2- Anesthesiologist class one and two American Society of Anesthesiology (ASA) health standards that will undergo urological surgery. 3. Parental consent for participation or continued study

Exclusion criteria

Exclusion criteria: 1- History of barbiturates 2- Complications of anesthesia, such as bleeding 3- Serum cardiovascular breakdown due to underlying heart disease 4. A history of acute pulmonary failure or severe renal failure

Design outcomes

Primary

MeasureTime frame
The incidence of agitation in children. Timepoint: After Completing the Operation, When Awakening in the Recovery and the Duration of the Recovery. Method of measurement: Table of Contents(Sedation-Agitation Scale) and Questionnaire.

Secondary

MeasureTime frame
Duration of Anesthesia and Recovery. Timepoint: Duration of Anesthesia for Minutes and Minutes of Recovery. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public Contactmaryam gholizadeh

Sabzevar University of Medical Sciences

gholizadehm1@mums.ac.ir+98 51 3821 3525

Outcome results

None listed

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