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Clinical Trials/CTRI/2016/11/007463
CTRI/2016/11/007463
Active, not recruiting
未知

The comparison of propopfol alone versus propofol with ketamine and propofol with fentanyl for sedation in Endoscopic Ultrasound

ILBS0 sites0 target enrollmentTBD
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ConditionsHealth Condition 1: null- ASA I,II and III patients scheduled for Endoscopic Ultrasound

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: null- ASA I,II and III patients scheduled for Endoscopic Ultrasound
Sponsor
ILBS
Status
Active, not recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional

Investigators

Sponsor
ILBS

Eligibility Criteria

Inclusion Criteria

  • •ASA physical status I,II and III patients scheduled for day care endoscopic ultrasongraphy

Exclusion Criteria

  • •Refusal to participate in the study.
  • •History of allergy to propofol.
  • •Patients having cardiac disease, impaired renal function,uncontrolled hypertension, uncontrolled thyroid dysfunction, patients on antipsychotic medication
  • •Pregnant and lactating mothers

Outcomes

Primary Outcomes

Not specified

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