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Effective Dose of Remimazolam Combined With Propofol in Painless Gastroscopy

Not Applicable
Completed
Conditions
Effect of Drug
Interventions
Registration Number
NCT05876793
Lead Sponsor
Sichuan Provincial People's Hospital
Brief Summary

This study used sequential method(Dixon's up and douwn) to determine the effective dose of remiazolam combined with propofol in painless upper gastrointestinal endoscopy

Detailed Description

Remimazolam tosylate is a novel benzodiazepine drug that can be used for gastrointestinal sedation. However, some studies have reported that the sedative effect of using remimazolam alone is poor, and the patient's body movements are obvious, which affects the operation of endoscopists. Propofol, as a commonly used sedative drug, has good sedative effects, but has a high incidence of adverse events, especially cardiovascular system inhibition. Therefore, this study will explore the effective dose of remimazolam combined with propofol, reduce the adverse events of propofol and increase the sedative efficacy of remimazolam. This study only set up one study group, fixed the dosage of propofol, adjusted the dosage of Remimazolam to meet the appropriate sedation requirements for patients. Patients with successful sedation were judged to have a negative reaction, while patients with failed sedation were judged to have a positive reaction. A sequential chart was drawn based on the sedation situation until 7 positive negative reaction intersections were found, and the study ended

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
22
Inclusion Criteria
  • ASA grading I to II, with a BMI of 18 to 30 kg/m2
Exclusion Criteria
  • Uncontrolled severe hypertension, previous history of abnormal anesthesia, unstable angina and myocardial infarction, abnormal liver and kidney function, acute upper respiratory tract infection, suspected difficulty in the airways, allergies to opioids, milk, eggs, and propofol, long-term use of sedative and analgesic drugs.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SEQUENTIAL
Arm && Interventions
GroupInterventionDescription
remimazolam tosylateRemimazolam tosilateThe fixed dose of propofol in this study was 0.5mg/kg, with an injection time of 30 seconds. Subsequently, remimazolam was administered at an initial dose of 0.1mg/kg. After 1 minute of administration, sedation was evaluated using MOAA/S. When the MOAA/S score was ≤ 1, endoscopic examination could begin. If the patient did not show physical activity or coughing, sedation was considered successful, and the next patient's medication dose was reduced by 0.02mg/kg; On the contrary, if sedation fails, the next patient will receive an additional 0.02mg/kg of medication.
Primary Outcome Measures
NameTimeMethod
Incidence of body movements or coughingDay 1

Incidence of body movements or coughing=(Number of people experiencing physical activity or coughing/total number of people studied)

Secondary Outcome Measures
NameTimeMethod
Sedation success timeDay 1

MOAA/S≤1

full alert timeDay 1

The time from the last administration to the first MOAA/S score of 5 points when the patient reaches 5 points in three consecutive MOAA/S scores

incidence of adverse eventsDay 1

Mainly including respiratory adverse events and circulatory adverse events

Inspection timeDay 1

The time from the beginning of the endoscopy to the exit of the examination mirror from the oral cavity

Trial Locations

Locations (1)

Sichuan Provincial People's Hospital

🇨🇳

Chengdu, Sichuan, China

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