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Explore the Advantages of Remimazolam Used on Gastroscopy

Explore the Advantages of Remimazolam Used on Gastroscopy : A Large Sample, Multicenter, Randomized, Double-blind, Parallel-controlled Clinical Study

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05429086
Enrollment
287
Registered
2022-06-23
Start date
2022-06-30
Completion date
2022-08-31
Last updated
2022-06-23

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

Conditions

Induction of Anesthesia

Keywords

remimazolam, propofol

Brief summary

There are many different types of intravenous anesthetics used in gastroscopy, but each type of drug has its advantages and disadvantages,remimazolam is a novel ultra-short-acting benzodiazepine with rapid onset and recovery, low circulatory depression, and rapid reversal of sedation by flumazenil,remimazolam may be another relatively ideal sedative-hypnotic option for anesthesiologists and gastrointestinal endoscopists. The purpose of this study was to explore whether remimazolam combined with propofol is safer and more effective than remimazolam alone or propofol alone in gastrointestinal endoscopy.

Detailed description

Sedation for gastroscopy is still a topic of debate in the global anesthesia and gastroenterology communities, and the sedation protocols of anesthesiologists and endoscopists vary widely. There are many different types of intravenous anesthetic drugs used in gastroscopy, but each type of drug has its advantages and disadvantages, and the most common protocol in anesthesia practice is an opioid (e.g., fentanyl) combined with a sedative-hypnotic drug (e.g., propofol and midazolam). But these protocols usually have limitations with propofol mainly focusing on respiratory depression and circulatory depression, in which perioperative hypotension should be considered a serious public health problem and should be taken seriously by clinicians, while midazolam has a long onset of action and a long recovery time. Therefore, there is an urgent clinical need for a fast-onset, fast-recovery drug with a high safety profile to solve this current dilemma. As a new ultra-short-acting benzodiazepine with rapid onset and recovery, low circulatory depression, and rapid reversal of sedation by flumazenil, remimazolam may be another relatively ideal sedative-hypnotic option for anesthesiologists and gastrointestinal endoscopists. The drug was approved for procedural sedation in 2020, and there are many studies on the use of remimazolam versus propofol in gastrointestinal endoscopy sedation. A non-inferiority clinical study of remimazolam tosilate in the upper gastrointestinal tract showed that remimazolam had a sedation success rate no lower than that of propofol, a longer onset of sedation than propofol, but a shorter time to full consciousness than propofol, and a significantly lower incidence of adverse events than propofol. These findings suggest that remimazolam is indeed safer than propofol, but its depth of sedation may be inferior to that of propofol. For clinical workers, it is also essential to have good depth of sedation while ensuring safety. Therefore, considering the above, we hypothesized that the use of remimazolam in combination with propofol in gastrointestinal endoscopy could meet clinical sedation needs and also reduce the incidence of respiratory depression and circulatory depression, which have not been reported. The purpose of this study was to determine whether remimazolam combined with propofol is safer and more effective than remimazolam alone or propofol alone in gastrointestinal endoscopy.

Interventions

DRUGRemimazolam combined propofol

Remimazolam combined propofol

DRUGRemimazolam

remimazolam only

DRUGPropofol

propofol only

Sponsors

Sichuan Provincial People's Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
TRIPLE (Subject, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Patients who are to undergo painless gastroscopy 2. Patients aged 18 - 80 years, regardless of gender 3. 18 \< BMI \< 30 kg/m2. 4. American Society of Anesthesiologists (ASA) classification of I-III.

Exclusion criteria

1. Preoperative hypertensive patients \>180/110 mm Hg or hypotensive patients \<80/50 mm Hg. 2. Heart rate \<50 beats/min. 3. A history of acute inflammation of the respiratory tract that has not been cured within 2 weeks; severe metabolic diseases of the heart, brain, lungs, liver, kidneys and diabetes mellitus; previous heart attack, severe myocardial, ischemia, severe atrioventricular block 4. Those who may have or have had a difficult airway or a history of recovery from abnormal surgical anesthesia 5. Patients with significant electrolyte disturbances such as hyperkalemia 6. Patients with a history of long-term use of immunosuppressive agents such as hormones or adrenal cortical suppression 7. Patients with known allergy to emulsions and opioids 8. Those with combined use of other sedative and analgesic drugs within the preoperative period (including injections, oral and use of related proprietary Chinese medicines) 9. Those suspected of abusing narcotic analgesics or sedatives 10. Those who have neuromuscular system diseases, mental diseases, etc. who do not cooperate and cannot communicate.

Design outcomes

Primary

MeasureTime frameDescription
Incidence of hypotensionDay 120% lower blood pressure than before the drug was administered

Secondary

MeasureTime frameDescription
Sedation success timeDay 1MOAA/S score ≤ 3
Injection painDay 1the pain score when give the subjects administration
Orientational force scoreDay 1ask the participants questions to evaluate
Ataxia ScaleDay 1teach the participants some motions , then ask them repeat the motions

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 8, 2026