Not Yet RecruitingNot Applicable

The Efficacy and Safety of Robotic Bronchoscopy System-Assisted Stent Placement in Patients with Malignant Central Airway Stenosis

30 participantsStarted 2025-02-15

Plain-language summary

The primary aim of this research is to assess the efficacy and safety of the bronchial navigation positioning equipment in assisting stent implantation for malignant central airway stenosis while guaranteeing the safety of the participants and the scientificity of the clinical trial.

Who can participate

Age range18 Years

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion criteria

✓. Age ≥ 18 years, regardless of gender;
✓. Patients voluntarily consent to airway stent implantation and meet the requirements for airway stent implantation under general anesthesia;
✓. Confirmed as having malignant central airway stenosis through bronchoscopy and being ineligible for surgery or refusing surgery, and in need of airway stent implantation.

Exclusion criteria

✕. Severe dysfunction of the heart, lungs, liver, or kidneys, intolerant of bronchoscopic treatment;
✕. Apparent coagulation dysfunctions;
✕. Pregnant or lactating women, or participants with a pregnancy plan during the study period;
✕. Patients with implanted cardiac pacemakers, implanted defibrillators, or other active implants;
✕. Participants allergic to photosensitizers or anesthetics, or with a history of multiple severe allergies or hereditary allergies;
✕. Participants who have participated in or are currently participating in drug clinical trials within the past 3 months, or in other medical device clinical trials within the past 30 days; Other circumstances that the investigator considers inappropriate for participation in this clinical trial.

What they're measuring

The success rate of stent placement

Timeframe: During the bronchoscopy

Trial details

NCT IDNCT06832943

SponsorGuangzhou Medical University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2025-12-31

Contact for this trial

Changhao Zhong

020-81566640 vast1982@126.com

View on ClinicalTrials.gov More Airway Stenosis trials