Skip to main content
Clinical Trials/CTRI/2022/05/042453
CTRI/2022/05/042453Not yet recruiting未知

A comparative study to evaluate the safety and efficacy of two different doses of oxytocin boluses in elective caesarean sections.

Department of Anaesthesia0 sites0 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
未知
Status
Not yet recruiting

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Inclusion Criteria

  • ASA grade II, Elective LSCS under Spinal Anaesthesia, Singleton pregnancy

Exclusion Criteria

  • Refusal of patient
  • Emergency LSCS
  • History of allergy to oxytocin
  • Placenta previa/accreta
  • Polyhydramnios
  • >2 Previous Caesarean sections
  • Multifetal Pregnancy
  • Contra-indications for Spinal Anaesthesia
  • Inadequate Spinal Anaesthesia or conversion to General Anaesthesia

Investigators

Similar Trials

A study to evaluate the safety and... | Clinical Trial