Antepartum Hemorrhage Clinical Trial
Official title:
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
Verified date | November 2015 |
Source | Kasr El Aini Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | Egypt: Institutional Review Board |
Study type | Observational |
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 .
Status | Active, not recruiting |
Enrollment | 124 |
Est. completion date | November 2015 |
Est. primary completion date | November 2015 |
Accepts healthy volunteers | No |
Gender | Female |
Age group | 18 Years to 40 Years |
Eligibility |
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 |
Observational Model: Cohort, Time Perspective: Prospective
Country | Name | City | State |
---|---|---|---|
n/a |
Lead Sponsor | Collaborator |
---|---|
Kasr El Aini Hospital |
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pleth Variability Index | 8 months | No | |
Secondary | hemoglobin level | 8 months | No |
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