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Clinical Trials/CTRI/2018/12/016756
CTRI/2018/12/016756CompletedPhase 4

Efficacy of Granisetron for prevention of Post-Spinal anaesthesia shivering, nausea and vomiting in parturients undergoing caesarean section

Maulana Azad Medical College0 sites0 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
Phase 4
Status
Completed

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • 1. Parturients scheduled for elective caesarean delivery under spinal anaesthesia
  • 2. Aged 20-45 years
  • 3. Full term singleton pregnancy

Exclusion Criteria

  • 1. Parturient with contra-indications to regional anaesthesia
  • 2. ASA Physical Status > II
  • 3. Allergy to 5-HT3 Antagonists
  • 4. Morbidly Obese
  • 5. Placenta Previa
  • 6. Use of vasodilators
  • 7. Pre-operative body temperature >38 C or < 36.5 C

Investigators

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