Application of Low-dose Muscle Relaxants in Bronchoscopic Interventional Procedures
Launched by HARBIN MEDICAL UNIVERSITY · Jun 15, 2025
Trial Information
Current as of June 27, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying how using a small dose of muscle relaxants during bronchoscopy—a procedure that looks inside the lungs—affects patients compared to not using these relaxants. Researchers want to see if the muscle relaxants make it easier and safer to insert the breathing tube after anesthesia, reduce spasms in the throat, lessen coughing and movement during the procedure, and help patients recover better afterward.
The study is open to adults aged 18 and older who are having planned bronchoscopic surgery lasting at least 20 minutes and are generally healthy enough for anesthesia. People with certain health issues, like severe heart or kidney problems, very high weight, or a history of breathing or anesthesia difficulties, cannot join. Participants will be divided into two groups: one will receive a low dose of muscle relaxants during anesthesia, and the other will not. The team will then observe how well each method works and how safe it is. If you or a family member are preparing for this type of lung procedure and meet the criteria, this study might be an option to discuss with your doctor.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • 1. Patients undergoing elective electronic bronchoscopic interventional surgery;
- • 2. Age 18 years or older;
- • 3. American Society of Anesthesiologists (ASA) I-III;
- • 4. The duration of bronchoscopic surgery \>=20min;
- • 5. Through pre-anesthesia assessment, the patient/family member has informed consent and signed the consent form;
- • 6. The general clinical information of the patient is complete.
- Exclusion Criteria:
- • 1. Patients with predictable difficult airway;
- • 2. Small mouth opening (\<2 transverse fingers);
- • 3. Combined with severe cardiovascular disease, abnormal liver and kidney function;
- • 4. Morbidly obese patients with body mass index (BMI) greater than 35kg/m\^2;
- • 5. Has a history of gastroesophageal reflux disease.
- • 6. High risk of reflux aspiration;
- • 7. Those who have a history of abnormal surgical anesthesia recovery in the past;
- • 8. Patients with mental illness and previous allergies to conventional anesthetic drugs.
About Harbin Medical University
Harbin Medical University is a prominent research institution located in Harbin, China, dedicated to advancing healthcare through innovative medical education and clinical research. With a strong emphasis on interdisciplinary collaboration, the university fosters a rigorous academic environment that supports a diverse range of clinical trials aimed at improving patient outcomes and addressing pressing health challenges. Its commitment to scientific excellence and ethical standards positions Harbin Medical University as a key player in the global medical research landscape, contributing valuable insights and breakthroughs in various fields of medicine.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Harbin, Heilongjiang, China
Patients applied
Trial Officials
SHI Jinghui SHI
Study Director
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported