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To compare the incidence of post operative delirium with dexmedetomidine and fentanyl in postoperative cardiac patients 12th hourly for 7 days in ICU.

Phase 4
Conditions
Health Condition 1: I00-I99- Diseases of the circulatory systemHealth Condition 2: I20-I25- Ischemic heart diseases
Registration Number
CTRI/2024/07/071553
Lead Sponsor
Institue of medical science and sum hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.Patients of age group 18-80 years scheduled for on pump cardiac surgeries.

Exclusion Criteria

1.Patients not giving consent

2.Patients with severe congestive heart failure,(ejection fraction less than 40),second degree heart blocks,neurological disorders,renal and liver failures.

3.If patient is hypotensive preoperatively.

4.If patient baseline heart rate is less than 55per min.

5.If patient has pacemaker insitu.

6.Patient getting reoperated.

7.Patient hypersensitive to opioids and known drug allergies.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To compare the incidence of postopertive delirium(confusion assessment method)with dexmedetomidine and fentanylTimepoint: 12th hourly for 7 days.
Secondary Outcome Measures
NameTimeMethod
Duration of sedation and analgesia,trail of extubation done after 12 hours of shifting the patient to ICU, ,incidence of tachyarrythmias,haemodynamic parameters(HR,MAP,SPO2) and side effects like nausea and vomitingsTimepoint: 2,,6,12,24,48 hourly-sedation and analgesia
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