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A clinical trial to compare two methods of oxygenation,high flow nasal cannula versus conventional nasal cannula on oxygenation in patients who undergo Endoscopic Retrograde Cholangiopancreatography under sedation

Comparision of the effect of high flow nasal cannula versus conevtional nasal cannula on oxygenation in patients undergoing Endoscopic Retrograde Cholangiopancreatography under sedation - NIL

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/01/061007
Enrollment
86
Registered
2024-01-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: High flow nasal cannula: This study compares the effect of high flow nasal cannula in one group versus low flow nasal cannula on oxygenation in patients undergoing endoscopic retrograd

Sponsors

Bangalore medical college and research institute
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients willing to give informed written consent. Patients belonging to American Society of Anesthesiologist class 1,2 and 3. Patients scheduled to undergo endoscopic retrograde cholangiopancreatography

Exclusion criteria

Exclusion criteria: 1. Patients not willing to give informed written consent 2. Patients with anticipated difficult airway and known previous difficult intubation 3. Patients with severe cardiac disorders, respiratory disorders and renal disorders that necessitate general anesthesia with endotracheal tube 4. Patients with increased risk of aspiration 5. Patients undergoing emergency procedures 6. Tracheostomized patients

Design outcomes

Primary

MeasureTime frame
number of episodes of desaturation ,Spo2 90% during endoscopic retrograde cholangiopancreatography under sedationTimepoint: 2 hours

Secondary

MeasureTime frame
a)Number of events of hypoxia, defined as desaturation b)Lowest recorded SpO2% during the procedure. The mean values during the procedure will be compared between group A and B. c)Heart rate d)Blood pressure. Timepoint: Until the ERCP procedure is complete

Countries

India

Contacts

Public ContactRashmi N Patil

Bangalore Medical College and Research Institute

sandyaraghu@gmail.com9972212417

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026