Comparison between Intravenous and Intranasal dexmedetomidine for changes in vitals during laryngoscopy and endotracheal intubation

Phase 4

Not yet recruiting

• Conditions: Bilateral inguinal hernia, with obstruction, without gangrene,

• Registration Number: CTRI/2024/01/061781
• Lead Sponsor: Peoples medical college bhopal

Brief Summary

After preoxygenation and premedication group 1 will be given intravenous dexmedetomidine 1ug/kg and group 2 will be given intranasal dexmedetomidine 1ug/kg. Both the groups compared for hemodynamic and analgesic stability.

Detailed Description

Not available

Study Timeline

• Study Start: 2024-01-25
• Last Update Posted: 2024-10-01

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

Age18years-60years ASA grade1 and2 Scheduled for Laryngoscopy and endotracheal Intubation.

Exclusion Criteria

• Lack of patient’s consent.
• Age<18yrsand>60yrs.
• ASA grade 3 and more.
• Patients with hypersensitivity to any of the drugs used.
• Pregnant and lactating mothers.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Hemodynamic stable	15 mins

Secondary Outcome Measures

Name	Time	Method
Analgesic stability	15 mins

Trial Locations

Locations (1)

Peoples hospital; 🇮🇳 Bhopal, MADHYA PRADESH, India

Peoples hospital

🇮🇳Bhopal, MADHYA PRADESH, India

Rohan kanthed

Principal investigator

9685256111

kanthedrk@gmail.com