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Effect of Ketamine on Sedation in Bronchoscopy

Comparison of the Effect of Three Different Ketamine doses on Quality of Sedation in Bronchoscopy

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20180416039326N17
Enrollment
90
Registered
2020-12-10
Start date
2020-11-21
Completion date
Unknown
Last updated
2021-01-05

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

Conditions

Bronchoscopy.

Interventions

Intervention 1: Intervention group 1 (The first group of Ketamine 0.2 mg/kg): Propofol 1.5 mg/kg is drawn into the pump syringe and according to the grouping, Ketamine is added to Propofol and the syr

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients who are candidates for Bronchoscopy Being at the age over 18 years old Patients whit ASA class 1 and 2

Exclusion criteria

Exclusion criteria: Patient disinclination Mental disorders History of chronic sedative drug use Opioid and alcohol use disorders History of any allergy to any medications use in the study Take sedative or analgesics 24 hours before the procedure

Design outcomes

Primary

MeasureTime frame
Sedation level based on Ramsay score. Timepoint: During the operation every 5 minutes and then in recovery room every 15 minutes, until recovery from recovery room. Method of measurement: questionnaire.

Secondary

MeasureTime frame
Heart Rate. Timepoint: Before the operation, During the operation every 5 minutes and then in recovery every 15 minutes, until recovery from recovery. Method of measurement: monitoring.;Systolic blood pressure. Timepoint: Before the operation, During the operation every 5 minutes and then in recovery every 15 minutes, until recovery from recovery. Method of measurement: monitoring.;Diastolic blood pressure. Timepoint: Before the operation, During the operation every 5 minutes and then in recovery every 15 minutes, until recovery from recovery. Method of measurement: monitoring.;Mean Atrial Pressure. Timepoint: Before the operation, During the operation every 5 minutes and then in recovery every 15 minutes, until recovery from recovery. Method of measurement: monitoring.;Percentage of arterial oxygen saturation. Timepoint: Before the operation, During the operation every 5 minutes and then in recovery every 15 minutes, until recovery from recovery. Method of measurement: monitoring.;Complications during the procedure (hypo tension, hypertension, tachycardia, bradycardia, pain ...). Timepoint: During the operation every 5 minutes minutes. Method of measurement: questionnaire.;Complications in recovery (vomiting nausea ...). Timepoint: in recovery every 15 minutes, until recovery from recovery. Method of measurement: questionnaire.;Duration of stay in recovery. Timepoint: per minutes. Method of measurement: questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamidraza Shetabi

Esfahan University of Medical Sciences

hamidshetabi@med.mui.ac.ir+98 31 3620 2020

Outcome results

None listed

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