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Trials / Completed

CompletedNCT04264234

Management Of Placenta Previa Cases And Determination Of Hospitalization Criteria

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
98 (actual)
Sponsor
Ege University · Academic / Other
Sex
Female
Age
Healthy volunteers
Accepted

Summary

Placenta previa cases are one of the difficult groups of patients to manage in modern obstetrics. When the literature is evaluated extensively, no clear information can be seen especially in terms of hospitalization time. Inpatient follow-up of this patients has negative effects like hospital infections in terms of the patient, workload in terms of health personnel and financial losses in terms of the country's economy. Placenta previa cases are complicated patients in which generalizations cannot be easily performed and they should be monitored at third level hospitals. In addition, care should be personalized considering the many reasons. In this study, placenta previa cases will be followed up at 28th gestational week and evaluated at 32nd week by vaginal ultrasonography and MRI and this follow-up will continue until delivery. Thus, in this study, it was aimed to determine the parameters that would allow systematic personalization of health service in this particular patient group by making risk assessment of placenta previa cases.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTVaginal UltrasonographyPlacenta previa cases will be evaluated at 32nd week by vaginal ultrasonography for invasion anomaly and preterm birth.
DIAGNOSTIC_TESTMagnetic Resonance ImagingPlacenta previa cases will be evaluated at 32nd week by MRI for invasion anomaly and preterm birth.

Timeline

Start date
2018-11-13
Primary completion
2020-02-01
Completion
2020-02-01
First posted
2020-02-11
Last updated
2022-03-23

Locations

1 site across 1 country: Turkey (Türkiye)

Source: ClinicalTrials.gov record NCT04264234. Inclusion in this directory is not an endorsement.

Management Of Placenta Previa Cases And Determination Of Hospitalization Criteria (NCT04264234) · Clinical Trials Directory