The Application of Balanced Propofol Sedation in Fiberoptic Bronchoscopy

• Status: Completed
• Trial end date: 2024-01-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to investigate the feasibility of using balanced propofol sedation for bronchoscopy. And screen out the optimal balanced propofol sedation compatibility plan.

• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: The Affiliated Hospital of Qingdao University
• Treatments: Dsuvia; Midazolam; Propofol; Sufentanil

Criteria

Inclusion Criteria:

1. American Society of Anesthesiologists classes I-IV ;

2. Patients undergo painless bronchoscopy, including bronchoscopic biopsy (bronchoscopic lesion biopsy, bronchial mucosal biopsy, bronchoscopic transmural lung biopsy, bronchoscopic needle aspiration biopsy) ,bronchoalveolar lavage and bronchoscopic treatment;

3. Normal communication skills and able to cooperate in completing this study;

4. Patients who voluntarily accept this experimental study and sign the "Trial Informed Consent Form".

Exclusion Criteria:

1. Patients with contraindications or allergies to anesthesia;

2. Individuals with a history of alcoholism or drug abuse;

3. Patients with contraindications for puncture of the cricoid membrane;

4. Patients with mental or neurological disorders, taking anti anxiety/depression drugs, or primary diseases with laboratory evidence indicating possible changes in hormone levels;

5. Patients with difficulty in language communication, poor understanding ability, and inability to cooperate in completing experimental studies;

6. Patients who require laryngeal mask or tracheal intubation for assisted ventilation during the examination process;

7. Patients undergoing rigid bronchoscopy treatment;

8. Patients who refuse to receive sedation or have not signed the "Trial Informed Consent Form".