An Observational study to assess role of Transnasal Humidified Rapid Insufflation Ventilatory Exchange with Target Controlled Infusion as sole airway management during Endoscopic Retrograde Cholangiopancreatography
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Enrollment
- 56
- Locations
- 1
- Primary Endpoint
- To assess the number of episodes of desaturation and duration of desaturation
Study Overview
Brief Summary
Patients fulfilling the inclusion criteria are selected.The appropriate details are filled in the proforma and consent obtained. The primary objective is to assess the number of episodes of desaturation and duration of desaturation.The secondary outcomes would be to assess the total propofol used, end tidal co2, arterial blood gas at the beginning & end of procedure, need for rescue ventilation, time taken to respond to oral commands, incidence of sore throat or dryness, hemodynamics at thrive removal, patient satisfaction and results are withdrawn.
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Masking
- None
Eligibility Criteria
- Ages
- 18.00 Year(s) to 75.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Body mass index less than 40kg/m2 American Society of Anaesthesiologists(ASA 1-3).
Exclusion Criteria
- •Patients younger than 18 years of age Anticipated difficult airway.
- •P a r t u r i e n t Risk of aspiration Hemodynamic instability Heart disease Emergency surgeries Allergy to propofol Patient refusal Inability to give consent to the study.
Outcomes
Primary Outcomes
To assess the number of episodes of desaturation and duration of desaturation
Time Frame: Intraoperative ( Beginning to end of procedure)
Secondary Outcomes
- Total Propofol used(End Tidal Co2)
Investigators
Ilancheran J
Sri Ramachandra Institute of Higher Education and Research