Comparison of two modes of airway anesthesia before awake fibreoptic intubatio

Phase 1

• Conditions: Health Condition 1: K319- Disease of stomach and duodenum, unspecifiedHealth Condition 2: K87- Disorders of gallbladder, biliarytract and pancreas in diseases classified elsewhere

• Registration Number: CTRI/2020/09/027605
• Lead Sponsor: il Ratan Sircar Medical college and Hospital

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 November 2021

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

ASA physical status 1 and 2, modified Mallampati score 3 and 4

Exclusion Criteria

Patientâ??s refusal, Known history of allergy to the drugs under study, ASA physical status 3 or more, Patients on anticoagulants, Patients having sepsis and / or local site infection, Patients with known CVS or Respiratory disease, Patients with hepatic or renal disorders, History of drug abuse.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1. Patient comfort score during awake fibreoptic intubation <br/ ><br>2. cough and gag score during awake fibreoptic intubationTimepoint: during awake fibreoptic intubation procedure

Secondary Outcome Measures

Name	Time	Method
Hemodynamic variables are significantly differentTimepoint: during laryngoscopy, then at 1 min, 3 min, 5 min post intubation