Skip to main content
TrialFinder
TrialFinder is for informational purposes only and does not provide medical advice. Always talk to your doctor about whether a trial is right for you.
RECRUITINGPhase 4INTERVENTIONAL

Remimazolam for Bronchoscopy in High-Risk Patients

A Prospective, Randomized Controlled Clinical Study of the Effect of Remimazolam on the Incidence of Hypoxia in High-risk Patients Undergoing Painless Tracheoscopy

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Bronchoscopy is currently widely used for the diagnosis and treatment of various respiratory diseases. However, the operation of bronchoscopy is irritating, causes a strong stress response, and shares the airway with the patient, making the patient highly susceptible to respiratory and cardiovascular risks. Among these risks, hypoxia is the most common adverse event.Different drug regimens can be selected for anesthesia under deep sedation. The combination of analgesic agents can help reduce coughing during bronchoscopy. Therefore, we employ a combination of sedative and analgesic drugs for painless bronchoscopy procedures. Among sedatives, propofol is the most commonly used. However, due to its disadvantages, such as respiratory and circulatory depression, we have introduced a novel approach combining remimazolam for sedation. The aim is to investigate whether this new regimen, compared to traditional propofol-based sedation, can reduce the incidence of hypoxia, minimize circulatory depression, and lead to faster postoperative awakening and recovery. Additionally, we hope to observe fewer adverse events, such as perioperative nausea and vomiting, excessive secretions, dizziness, and chills.

Who May Be Eligible (Plain English)

Who May Qualify: - ASA Class Ⅲ - Ⅳ - Scheduled for elective painless bronchoscopy - Who Should NOT Join This Trial: - Age \< 18 years - Patients who are uncooperative(e.g. due to mental illness) - Patients who are on chronic use of opioids, benzodiazepine - class hypnotics, or antidepressants - Patients with a history of allergy to the anesthetics used - Patients who are anticipated to have a difficult airway - Body mass index(BMI)\<18.5kg/m² or \>30kg/m² - Preoperative oxygen saturation \<92% while breathing room air - Other:Patients who are deemed by the investigator to be unsuitable for participation in this trial Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * ASA Class Ⅲ - Ⅳ * Scheduled for elective painless bronchoscopy - Exclusion Criteria: * Age \< 18 years * Patients who are uncooperative(e.g. due to mental illness) * Patients who are on chronic use of opioids, benzodiazepine - class hypnotics, or antidepressants * Patients with a history of allergy to the anesthetics used * Patients who are anticipated to have a difficult airway * Body mass index(BMI)\<18.5kg/m² or \>30kg/m² * Preoperative oxygen saturation \<92% while breathing room air * Other:Patients who are deemed by the investigator to be unsuitable for participation in this trial

Treatments Being Tested

DRUG

propofol and alfentanil

General anesthesia with spontaneous breathing maintained is administered using propofol and alfentanil.

DRUG

remimazolam combined with propofol and alfentanil

General anesthesia with spontaneous breathing maintained is administered using remimazolam combined with propofol and alfentanil.

Locations (2)

The First Affliated Hospital, Zhejiang University School Of Medicine
Hangzhou, Zhejiang, China
Shaoxing City First People's Hospital
Shaoxing, Zhejiang, China