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Evaluation of anesthesia quality with three methods: "propofol + fentanyl " Vs "propofol + fentanyl + lidocaine" Vs "propofol + fentanyl + lidocaine + ketamine" in patients referred to the scoping ward

Evaluation of cough frequency and duration of recovery with three anesthesia methods: "Propofol + Fentanyl", "Propofol + Fentanyl + Lidocaine" and "Propofol + Fentanyl + Lidocaine + Ketamine" in patients referred to the scoping ward

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200921048789N2
Enrollment
100
Registered
2021-04-12
Start date
2021-04-21
Completion date
Unknown
Last updated
2021-04-26

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

Conditions

None listed

Interventions

Intervention 1: Intervention group: Group A includes patients in whom propofol + fentanyl has been used for sedation for scoping. Propofol-lipuro: initial dose 1mg/kg and repeat dose 0.5 mg/kg every 3

Sponsors

Artesh University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: All patients who are candidates for scoping in 501 Army Hospital in 2021

Exclusion criteria

Exclusion criteria: Age under 18 and over 70 years ASA classification 4 or 5 History of uncontrolled blood pressure History of Chronic Obstructive Pulmonary Disease (COPD) History of psychotic or neurological disorders History of seizures History of use of drugs affecting the central nervous system Pregnancy

Design outcomes

Primary

MeasureTime frame
Frequency of cough. Timepoint: During and after the intervention. Method of measurement: View on the patient bed.;Duration of recovery. Timepoint: After intervention. Method of measurement: View on the patient bed.

Secondary

MeasureTime frame
O2 saturation. Timepoint: During and after the intervention. Method of measurement: view on the patient's bed.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadreza rafiei

Artesh University of Medical Sciences

Rafiei_mohamadreza@yahoo.com+98 21 8609 6350

Outcome results

None listed

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