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Clinical Trials/NCT05295667
NCT05295667
Completed
Not Applicable

Combination of Doppler Measurements With Amniotic Fluid Volume for the Predicition of Perinatal Outcome in FGR

Istanbul Bakirkoy Maternity and Children Diseases Hospital1 site in 1 country100 target enrollmentJune 1, 2020
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ConditionsFetal Growth Retardation

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Fetal Growth Retardation
Sponsor
Istanbul Bakirkoy Maternity and Children Diseases Hospital
Enrollment
100
Locations
1
Primary Endpoint
the prediction power of adverse perinatal outcome with new doppler parameters ( such as AUCR)
Status
Completed
Last Updated
4 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The investigator contrived a prospective study of AUCR to compare its association to adverse perinatal outcomes with other established doppler parameters, such as CPR and UCR within a population of suspected FGR fetuses at term.

Registry
clinicaltrials.gov
Start Date
June 1, 2020
End Date
June 30, 2020
Last Updated
4 years ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Istanbul Bakirkoy Maternity and Children Diseases Hospital
Responsible Party
Principal Investigator
Principal Investigator

Osman Aşıcıoğlu

Associated Proffesor

Istanbul Bakirkoy Maternity and Children Diseases Hospital

Eligibility Criteria

Inclusion Criteria

  • •SİNGLETON PREGNANCİES WİTH FGR FETUSES
  • •AFTER 37th GESTATİONAL WEEKS

Exclusion Criteria

  • •SİNGLE OR MUTİPL FETAL ANOMALİES
  • •EVİDENCE OF İNTRAUTERİNE ENFECTİON

Outcomes

Primary Outcomes

the prediction power of adverse perinatal outcome with new doppler parameters ( such as AUCR)

Time Frame: 1 year

enterence to neonatal intensive care unit and severe fetal acidemia ( pH: \>7.10)

Study Sites (1)

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