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Clinical Trials/CTRI/2023/08/057104
CTRI/2023/08/057104
Recruiting
Phase 4

Comparison of inhalational anesthesia (Sevoflurane) and total intravenous anesthesia with propofol, dexmedetomidine on postoperative nausea and vomiting and postoperative recovery parameters in laparoscopic surgery - A prospective randomized controlled trial. - Nil

Apollo Hospitals Bilaspur0 sites0 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Apollo Hospitals Bilaspur
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • ASA Grade I and II
  • Scheduled for laparoscopic surgery under general anesthesia

Exclusion Criteria

  • 1\. Known allergy to study drug.
  • 2\. Use of antiemetic drug within 24 hour of surgery.
  • 3\. Morbid obesity (BMI \>40\)
  • 4\. Chronic use of opioids.
  • 5\. Patient with hepatic , renal and cardiovascular dysfunction.
  • 6\. Psychiatric patients.
  • 7\. Patient with history of motion sickness.

Outcomes

Primary Outcomes

Not specified

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