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Clinical Trials/PACTR201312000577386
PACTR201312000577386Not yet recruiting未知

Efficacy and safety of dexamethasone in prevention of intra operative nausea, vomiting and hypotension in obstetrics

MaCHS0 sites180 target enrollmentStarted: June 28, 2013Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Not yet recruiting
Sponsor
Enrollment
180

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 Year(s) to 40 Year(s) (—)
Sex
Female

Inclusion Criteria

  • All Women 18-40 years old undergoing caesarean sections under spinal anaesthesia and having
  • Consented to participate in the study.
  • Emancipated minors.
  • ASA 1and ASA 11

Exclusion Criteria

  • Patient¿s refusal to consent
  • Hypertension
  • History of allergy to dexamethasone
  • Severe systemic infections
  • History of active GI ulceration
  • History dexamethasone treatment in the last 24 hours
  • ASA 111 and above

Investigators

Sponsor
MaCHS

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