A study comparing two oxygen delivery devices to improve the patient safety and improve performance of EBUS procedures

Not yet recruiting

Conditions: Other intraoperative and postprocedural complications and disorders of respiratory system, not elsewhere classified,

Registration Number: CTRI/2025/06/088648

Lead Sponsor: Dr Ankita

Brief Summary: In this study, we intend to evaluate the efficacy and effectiveness of oxygenation through nasal airway and compare it to nasal prongs in patients undergoing endobronchial ultrasound guided procedures. We will compare two devices in terms of complications, procedural interruptions, and duration. We will also compare patients comfort with both devices. We hope the findings of our study will significantly improve patient safety and ease of performance of procedure

Detailed Description: Not available

Recruitment & Eligibility

Status: Not Yet Recruiting

Sex: All

Target Recruitment: 60

Inclusion Criteria

Able to give informed consent, spontaneously breathe throughout procedure, no history of cardiorespiratory or hepatic failure, baseline saturation more than 90%.

Exclusion Criteria

Age more than 80years, chronic hypoxemic, nasal bone fracture, uncorrectable coagulopathy, pregnant, arrythmias history, bmi more than 30, previous nasal surgery, cardiorespiratory or hepatic failure.

Study & Design

Study Type: Interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Desaturation events	10 minutes in recovery

Secondary Outcome Measures

Name	Time	Method
Procedural desaturation, interruptions and duration, coughing, nasal bleed and patients comfort	10 mins in recovery

Trial Locations

Locations (1): Indraprastha Apollo Hospital, Sarita Vihar , New Delhi
🇮🇳
South, DELHI, India
Indraprastha Apollo Hospital, Sarita Vihar , New Delhi
🇮🇳South, DELHI, India
Dr Ankita
Principal investigator
9582590674
ankitamehandiratta@gmail.com