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A study conducted in a tertiary care hospital comparing the sedative effects of Dexmedetomidine and Propofol infusion during middle ear operations.

Phase 4
Conditions
Health Condition 1: H758- Other specified disorders of middle ear and mastoid in diseases classified elsewhere
Registration Number
CTRI/2023/07/055887
Lead Sponsor
Dr. Chandamita Bhagabati
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Age: 18 -60 years.

2.Sex: both male and female.

3.ASA grade I and II.

4.Patients undergoing middle ear surgeries in a tertiary care hospital.

Exclusion Criteria

1.Pregnant or Lactating females.

2.Known drug allergies.

3. Active upper respiratory infection.

4.Psychological Disorders.

5. Patients with respiratory dysfunction/ Patients with OSA.

6.Obese patients.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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