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Prediction of Postpartum Hemorrhage With Uterine Artery Doppler Measurement

The Role of Uterine Artery Doppler Measurement to Predict the Amount of Postpartum Hemorrhage in Low Risk Term Pregnancy

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03229304
Enrollment
800
Registered
2017-07-25
Start date
2016-05-01
Completion date
2017-06-01
Last updated
2017-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postpartum Hemorrhage

Brief summary

The aim of the study is to evaluate the uterine artery doppler just before labour in term low risk pregnancies. And to investigate with this measurement if investigators could foreseen the amount of postpartum hemorrhage looking at decreased in the hematocrit values.

Interventions

None listed

Sponsors

Kanuni Sultan Suleyman Training and Research Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* singleton term pregnancies

Exclusion criteria

the pregnant women who have * polyhydramnios * Large for gestational age fetuses * multiple pregnancies * preterm labour * chorioamnionitis * history of atonia or postpartum hemorrhage

Design outcomes

Primary

MeasureTime frameDescription
To measure the uterine artery Pulsatility index in term pregnant women6-8 hour before the deliveryWith ultrasonography uterine artery doppler Pulsatility index (cm/s) will be measure
To measure the uterine artery Resistant index (cm/s) in term pregnant women6-8 hour before the deliveryWith ultrasonography uterine artery doppler Resistant index will be measure
To measure the uterine artery mean systolic/diastolic volume (cm/s) in term pregnant women6-8 hour before the deliveryWith ultrasonography Uterine artery doppler Mean systolic/diastolic volume (cm/s) ) will be measure

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026