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The effect of lidocaine spray to decrease propofol dosage

Comparison of the sedation effect of propofol with lidocaine spray versus isolated propofol admission during upper GI endoscopy in elective and outpatient patients

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20200526047573N1
Enrollment
160
Registered
2020-10-20
Start date
2020-05-20
Completion date
Unknown
Last updated
2020-11-09

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

Conditions

Diseases of upper digestive system which need endoscopy. Gastric ulcer

Interventions

Intervention 1: propofol (Razavi Pharmacy) at a dose of 50 µg/kg. Intervention 2: propofol at a dose of 50 µg/kg and a total of 3 puffs of 10% lidocaine spray (Caspian Tamin company) to the throat and

Sponsors

Babol University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patient age between 20 to 65 years old Patients requiring upper gastrointestinal endoscopy

Exclusion criteria

Exclusion criteria: Psychological disease Addiction Anemia Obesity Swallowing Disorders (Myasthenia gravis and Alzheimer's) Cardiac Disease Low blood pressure Bradycardia Hepatic Failure Kidney Disease

Design outcomes

Primary

MeasureTime frame
Propofol Dosage. Timepoint: At The End of Endoscopy. Method of measurement: Milligram per kilogram.;Nausea and Vomiting. Timepoint: At The End of Endoscopy. Method of measurement: Patient's clinical symptoms.;Respiratory Distress. Timepoint: At The End of Endoscopy. Method of measurement: Intercostal muscle retraction.;Heart Rate. Timepoint: At The End of Endoscopy. Method of measurement: Cardiac monitoring.;Blood Pressure. Timepoint: At The End of Endoscopy. Method of measurement: Non Invasive Blood Pressure Tools.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAlma Bigdeli

Babol University of Medical Sciences

dr.a.bigdeli67@gmail.com+98 11 3223 8301

Outcome results

None listed

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