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Comparison of Different Protocols of Fluid Therapy in Severe Preeclamptic Patients Under Spinal Anesthesia

A

Assiut University

Status and phase

Unknown
Early Phase 1

Conditions

Hypotension Drug-Induced

Treatments

Drug: Lactated Ringer

Study type

Interventional

Funder types

Other

Identifiers

NCT03478618
haemodynamics in preeclampsia

Details and patient eligibility

About

To compare the effect of two different protocol of fluid therapy in sever preeclamptic patients under spinal anesthesia : Hemodynamic and kidney function .

Enrollment

60 estimated patients

Sex

Female

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • more than 36 weeks gestation
  • singleton pregnant women planned for elective caesarian section

Exclusion criteria

  • patient refusal.
  • psychiatric disorders.
  • parturient <36 weeks gestation, twins, abnormal cardiotocography (CTG) tracing.
  • absolute contraindications for spinal anesthesia (patients refusal, raised intracranial pressure, hypovolemic states, abnormal coagulopathy).

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

Group R
Active Comparator group
Description:
30 patients will receive 15ml/kg/h lactated Ringer (LR) intraoperative.
Treatment:
Drug: Lactated Ringer
Group L
Active Comparator group
Description:
30 patients will receive 30ml/kg/h lactated Ringer (LR) intraoperative.
Treatment:
Drug: Lactated Ringer

Trial contacts and locations

0

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Central trial contact

Zein El Abadin Zarae Hassan, PhD

Data sourced from clinicaltrials.gov

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