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Clinical Trials/TCTR20160426003
TCTR20160426003Completed未知

A comparison of Phenylephrine Administration between Intravenous Bolus and Slow Injection in Treatment of Spinal Anesthesia-induced Hypotension on Bradycardia and Other Side Effects in Patients Undergoing Cesarean Section

none0 sites58 target enrollmentStarted: April 26, 2016Last updated:
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Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
58
Study OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 Years to 60 Years (—)
Sex
Female

Inclusion Criteria

  • •1.ASA physical status I or II
  • •2.Age ≥ 18 years old
  • •3.Singleton baby
  • •4.Term pregnancy (GA ≥ 37 weeks)

Exclusion Criteria

  • •1. Pregestational or gestational hypertension
  • •2. Cardiovascular disease
  • •3. Cerebrovascular disease
  • •4. Obstetric complications (eg. abruptio placenta , placenta previa)
  • •5. Known abnormal fetus
  • •6. History use of monoamine oxidase inhibitor (MAOI) or other drugs that prlong heart conduction
  • •7. Other medications except spinal bupivacaine and spinalmorphine before baby delivery

Investigators

Sponsor
none

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