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Clinical Trials/CTRI/2021/06/033990
CTRI/2021/06/033990
Not Yet Recruiting
Phase 4

A comparative study of haemodynamic responses of propofol induction between BIS guided dose and sleep dose

Sentila Shangne0 sites0 target enrollmentTBD
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Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Sentila Shangne
Status
Not Yet Recruiting
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Sentila Shangne

Eligibility Criteria

Inclusion Criteria

  • •Elective surgeries under general anaesthesia
  • •Patients with a signed informed written consent form

Exclusion Criteria

  • •Patient refusal
  • •History of cardiac diseases like dilated cardiomyopathy,CCF, Arrhythmias etc
  • •History of uncontrolled hypertension and hypotension
  • •Patients with hepatic or renal dysfunction, pregnancy or any serious medical conditions that would interfere with cardiovascular response
  • •Patients with history of allergy to any GA drugs
  • •Cases lasting less than 30mins

Outcomes

Primary Outcomes

Not specified

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