Role of Doppler Echoflowmetry to Define Risk Factors for the Development of Complications in Twin Pregnancies

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18-44
SponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna

About this trial

The goal of this observational study is to evaluate the outcomes of twin pregnancies referred to our center, in order to understand whether the use of different guidelines over time, with more systematic follow-up timing, has improved their management by reducing adverse events. All this would provide us with useful information for a better understanding of the effects of twinhood on pregnancy outcomes, so that we have more accurate information in counseling with patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age > 18 years

Twin Pregnancy

Ultrasound monitoring and delivery occurred at Policlinico S Orsola in Bologna, Italy

Written informed consent form obtained from the patient

Disqualifiers

Completion of delivery at another facility

Desire to undertake the Voluntary Interruption of Pregnancy

Refusal to undergo instrumental monitoring and subsequent follow-up at our center

Trial population

The study population will consist of patients with twin pregnancies, regardless of chorionicity, who access the Pregnancy at Risk outpatient clinic at our center to perform the specific diagnostic care pathway.

Trial design

Design model

Cohort

Time perspective

Other

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Consequences of twinning on maternal and fetal hemodynamics

Evaluation of the effects and consequences of twinning on maternal and fetal hemodynamics during pregnancy.

Time frame
up to 100 weeks

Secondary outcomes

1

Potential risk factors for the development of adverse maternal or fetal outcomes

Assessment of the presence of specific and potential risk factors for the development of adverse maternal or fetal outcomes

Time frame
up to 100 weeks
2

Assessment of the presence of any different outcomes in relation to the guidelines applied in the past

Compare the guidelines applied in the past with the results obtained from the outcomes

Time frame
up to 100 weeks

Other outcomes

Sponsors and contacts

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