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Clinical Trials/CTRI/2014/08/004818
CTRI/2014/08/004818
Recruiting
未知

The effect of midazolam and dexmedetomidine sedation on duration of supraclavicular brachial plexus block: a randomised controlled study.

Indira Gandhi Institute of medical Sciences0 sites60 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: null- Trauma or other surgery of upper limb
Sponsor
Indira Gandhi Institute of medical Sciences
Enrollment
60
Status
Recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. ASA grade 1 \& 2
  • 2, Patient scheduled for upper extremity surgery where supraclavicular brachial plexus block is indicated

Exclusion Criteria

  • 1\. known contraindication to brachial plexus block (patient refusal, coagulopathy, local infection)
  • 2\. known allergy to bupivacaine, midazolam and dexmedetomidine
  • 3\. concommittant us of analgesics or sedatives
  • 4\. history of significant cardiovascular, respiratory, neurological, psychiatric, hepatic or renal disease
  • 5\. failed brachial plexus block

Outcomes

Primary Outcomes

Not specified

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