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Clinical Trials/IRCT20151221025641N5
IRCT20151221025641N5
Recruiting
Phase 3

Comparing the effectiveness of propofol-remifentanil with propofol-dexmedetomidine in reducing pain after awake craniotomy surgery

Tehran University of Medical Sciences0 sites64 target enrollmentTBD
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ConditionsAwake craniotomy.Other disorders of brain in diseases classified elsewhere

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Awake craniotomy.
Sponsor
Tehran University of Medical Sciences
Enrollment
64
Status
Recruiting
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • •The patient should be a candidate for craniotomy surgery using the sleep\-awake\-asleep method;
  • •The patient does not have a previous craniotomy history;
  • •The patient does not have a contraindication for full anesthesia;
  • •The patient's age is between 20 and 50 years;
  • •The patient does not have a history of allergy to any of the drugs under study.

Exclusion Criteria

  • •In addition to craniotomy, the patient needs to perform another surgery at the same time;
  • •Breast feeding;
  • •The patient has simultaneously heart, renal or liver failure;
  • •Severe obesity (BMI\>30 kg/m2\);

Outcomes

Primary Outcomes

Not specified

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