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Prophylactic Phenylephrine Co-administration During Caesarean Section

NCT04005664 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2019-07-02

No results posted yet for this study

Summary

This single centre prospective alternating intervention study will aim to compare prophylactic phenylephrine given in the first litre of Ringers lactate as co-load in healthy patients having an elective caesarean section under spinal anaesthesia at Edendale Hospital to the existing national protocol guideline - for the treatment of obstetric spinal hypotension.

Conditions

  • Cesarean Section Complications
  • Anesthesia Complication

Interventions

DRUG

Phenylephrine

Prophylactic phenylephrine infusion as part of fluid coload

Sponsors & Collaborators

  • University of KwaZulu

    lead OTHER

Principal Investigators

  • David G Bishop, PhD · University of KwaZulu

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-05-01
Primary Completion
2018-12-31
Completion
2018-12-31

Countries

  • South Africa

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04005664 on ClinicalTrials.gov