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The effect of dexmedtomidine and fentanyl on hemodynamic indicies in Stereotaxic surgeries.

Comparison effect of fentanyl and dexmedtomidine on hemodynamic changes during stereotaxic surgeries

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20110528006617N5
Enrollment
68
Registered
2021-01-30
Start date
2017-03-21
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

General Anesthesia. Other complications of anesthesia

Interventions

Intervention 1: The first intervention group: Initially,personal consent is obtained from the patients.Then the patient is placed on the perating bed and standard monitoring devices including pulsoxim

Sponsors

Esfahan university of medical sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Age btween 18-65 years old Patients who consent to the informed consent to participate in the study. Patient with american society of anesthesiology physical status class 1,2(ASA I,II)

Exclusion criteria

Exclusion criteria: Patients who have bradycardia and heart block. Patients who have anticoagulant drugs. Patients who have drugs affect on hemodynamic status.

Design outcomes

Primary

MeasureTime frame
Systolic blood pessure. Timepoint: Before intervention and 30,60,90,120 minutes after intervention and recovery time. Method of measurement: Mm-hg, sphygmomanometer.;Diastolic blood pressure. Timepoint: Before intervention and 30,60,90,120 minutes after intervention and recovery time. Method of measurement: Mm-hg, sphygmomanometer.;Heart rate. Timepoint: Before intervention and 30,60,90,120 minutes after intervention and recovery time. Method of measurement: ECG monitor.;Mean arterial pressure. Timepoint: Before intervention and 30,60,90,120 minutes after intervention and recovery time. Method of measurement: Mm-hg, sphygmomanometer.;O2 saturation. Timepoint: Before intervention and 30,60,90,120 minutes after intervention and recovery time. Method of measurement: O2 saturation percentage , pulse oximeter device.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMina Foroughi

Esfahan University of Medical Sciences

Mina.f1994@gmail.com+98 31 3528 4210

Outcome results

None listed

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