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Clinical Trials/NCT02614053
NCT02614053
Unknown
Not Applicable

Continuous Non Invasive Monitoring of Both Plethysmography Variability Index and Total Hemoglobin During Cesarean Section for Antepartum Hemorrhage As a Method For Early Detection of Bleeding

Kasr El Aini Hospital0 sites124 target enrollmentMarch 2015
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ConditionsAntepartum Hemorrhage

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Antepartum Hemorrhage
Sponsor
Kasr El Aini Hospital
Enrollment
124
Primary Endpoint
Pleth Variability Index
Last Updated
10 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

The purpose of this study is to evaluate the use of continuous noninvasive intraoperative plethesmography variability index in conjunction with Hemoglobin levels monitoring using Masimo Radical-7™ Pulse CO-Oximeter during elective cesarean sections in patients with antepartum and intrapartum hemorrhage as a guide for fluid and blood transfusion practice .

Registry
clinicaltrials.gov
Start Date
March 2015
End Date
November 2015
Last Updated
10 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Kasr El Aini Hospital
Responsible Party
Principal Investigator
Principal Investigator

ahmed elsakka

lecturer of anaesthesia faculty of medicine cairo university

Kasr El Aini Hospital

Eligibility Criteria

Inclusion Criteria

  • •Anesthesiologist (ASA) Physical status I - II.
  • •patients aged from 18 to 40 years
  • •full-term multigravida parturients
  • •antepartum hemorrhage
  • •singleton fetus

Exclusion Criteria

  • •Patients with known cardiac problem
  • •peripheral circulatory failure of the upper extremities
  • •significant liver disease
  • •significant renal disease
  • •significant coagulopathy

Outcomes

Primary Outcomes

Pleth Variability Index

Time Frame: 8 months

Secondary Outcomes

  • hemoglobin level(8 months)

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