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Clinical Trials/CTRI/2017/06/008915
CTRI/2017/06/008915
Not yet recruiting
Phase 4

A comparison of efficacy of prophylactic infusion of Phenylephrine versus Norepinephrine for the prevention of post spinal hypotension in parturients undergoing elective caesarean section- A randomized controlled trial

ALL INDIA INSTITUTE OF MEDICAL SCIENCES0 sites130 target enrollmentTBD

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
ALL INDIA INSTITUTE OF MEDICAL SCIENCES
Enrollment
130
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. WOMEN OF SINGLETON PREGNANCY WITH GESTATIONAL AGE OF MORE THAN 36 WEEKS OF GESTATION
  • 2\. ASA I AND II WOME

Exclusion Criteria

  • 1\. Patient refusal
  • 2\. Multiple gestation
  • 3\. Pregnancy with severe systemic illness (uncontrolled diabetes, hypertension, cardiac disease, etc.)
  • 4\. BMI \> 40 kg/m2
  • 5\. In active labour
  • 6\. Suspected obstetric complications ( like polyhydraminos, IUGR)
  • 7\. Patients in whom spinal anaesthesia is contraindicated (spinal abnormalities, infection at the site of injection, coagulopathies, raised intracranial tension)

Outcomes

Primary Outcomes

Not specified

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