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Clinical Trials/CTRI/2012/08/002934
CTRI/2012/08/002934
Completed
未知

Comparison of propofol with midazolam regarding arousal time from sedation during spinal anaesthesia in adult patients undergoing elective infraumbilical surgeries.

ORTH BENGAL MEDICAL COLLEGE0 sites110 target enrollmentTBD
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ConditionsHealth Condition 1: null- Either sex, age between 18 to 60 years, ASA I and ASA II, posted for elective infraumbilical surgical, gynaecological, or orthopaedic operations.

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: null- Either sex, age between 18 to 60 years, ASA I and ASA II, posted for elective infraumbilical surgical, gynaecological, or orthopaedic operations.
Sponsor
ORTH BENGAL MEDICAL COLLEGE
Enrollment
110
Status
Completed
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
ORTH BENGAL MEDICAL COLLEGE

Eligibility Criteria

Inclusion Criteria

  • •Patients of either sex, of age between 18 to 60 years complying to ASA I and ASA II criteria, who are posted for elective infraumbilical operations (be it surgical, gynaecological, or orthopaedic), of approximate 90 mins duration.

Exclusion Criteria

  • •a.Patient not willing to accept spinal anaesthesia
  • •b.Patient not willing to receive sedation during surgery under spinal anaesthesia
  • •c.Patient not willing to participate in the study
  • •d.Patient having any of the followingâ??
  • •Neurological Disease
  • •Local infection at the site of inducing the block
  • •Spinal deformity, past history of spine surgery or trauma
  • •Coagulopathy
  • •Psychiatric Illness
  • •Any history of allergy to the drugs to be used for the study

Outcomes

Primary Outcomes

Not specified

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