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Clinical Trials/EUCTR2007-002949-20-GB
EUCTR2007-002949-20-GBActive, not recruitingPhase 1

Randomised controlled trial comparing the effects of oxytocin 5 units IV bolus vs oxytocin 5 units IV infusion on cardiac output during caesarean section - Effect on cardiac output of oxytocin bolus vs. infusion

iverpool Women's NHS Foundation Trust0 sites32 target enrollmentStarted: February 15, 2008Last updated:
Drugs

Trial Snapshot

Phase
Phase 1
Status
Active, not recruiting
Sponsor
Enrollment
32

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional clinical trial of medicinal product

Eligibility Criteria

Inclusion Criteria

  • All patients who are due to undergo elective caesarean section under spinal anaesthesia at more than 37 weeks gestation; ASA grade 1 or 2; age 18 or over.
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

Exclusion Criteria

  • Conversion to general anaesthetic; placenta praevia; diabetes mellitus; pregnancy induced hypertension; chronic hypertension; patients requiring peri-operative therapeutic anti-coagulant therapy; pre operative anaemia; liver disease; chronic renal failure; history of anaphylaxis to oxytocin.

Investigators

Sponsor
iverpool Women's NHS Foundation Trust

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