Respiratory diseases
Conditions
Interventions
Experimental group:Esmketamine+propofol
Control group:Propofol
Sponsors
The First Affiliated Hospital of Zhengzhou University
Eligibility
Sex/Gender
All
Age
18 Years to 75 Years
Inclusion criteria
Inclusion criteria: 1. Patients to be examined by painless ultrasound bronchoscopy; 2. Age 18-65 years old, regardless of gender; 3. Body mass index (BMI) 18.5-30kg/m2; 4. The American Society of Anesthesiologists (ASA) is classified as grade I ~ III; 5. Voluntarily participate and sign informed consent.
Exclusion criteria
Exclusion criteria: 1. Patients who the investigator considered inappropriate to participate in the trial; 2. Patients with contraindications to sedation/anesthesia or previous history of abnormal recovery of sedation/anesthesia; 3. Those who are known to be allergic to local anesthetics, propofol, benzodiazepines, and opioids; 4. Have a history of serious heart, brain, liver, kidney, and metabolic diseases.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Occurrence of intraoperative hypotension;Improved anesthesia recovery time; | — |
Secondary
| Measure | Time frame |
|---|---|
| Vital signs;Time related indicators;Types and doses of drugs used during operation;Satisfaction score;Occurrence of adverse reactions; | — |
Countries
China
Contacts
Public ContactYunqi Lv
The First Affiliated Hospital of Zhengzhou University
Outcome results
None listed