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Clinical Trials/CTRI/2023/06/054141
CTRI/2023/06/054141
Not yet recruiting
Phase 3

asopharyngeal Airway as an adjunct to reduce Sedation Related Adverse Events during ERCP procedures

Department of GI Anaesthesiology0 sites0 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Health Condition 1: O- Medical and Surgical
Sponsor
Department of GI Anaesthesiology
Status
Not yet recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional

Investigators

Sponsor
Department of GI Anaesthesiology

Eligibility Criteria

Inclusion Criteria

  • 1\. All ASA I and II patients and without major comorbidities undergoing therapeutic ERCP procedure under moderate to deep sedation .
  • 2\. Patients who have given written, informed consent to participate in the study.

Exclusion Criteria

  • 1\. ASA I and IV patients
  • 2\. History of nasal bleed and coagulopathy
  • 3\. Cranio facial anomalies
  • 4\. Head and face trauma
  • 5\. Deviated Nasal Septum or external nasal pathology
  • 6\. Major systemic comorbidities
  • 7\. Very sick patients
  • 8\. Morbid obesity
  • 9\. Airway difficulty

Outcomes

Primary Outcomes

Not specified

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