Study of Maternal and Fetal Cardiovascular Function in Hypertensive States of Pregnancy

ConditionPreeclampsia
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorFundacion para la Formacion e Investigacion Sanitarias de la Region de Murcia

About this trial

The pharmacological treatment strategy is then tailored to the underlying hemodynamic phenotype of each patient. That is, rather than applying a one-size-fits-all treatment for all patients, therapy is tailored to the specific characteristics of how the cardiovascular system functions in each patient (e.g., whether the problem is more related to blood volume, vascular resistance, cardiac output, etc.). The goal is to personalize therapy to more effectively treat hypertensive states of pregnancy.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age greater than or equal to 18 years

Women with singleton and twin pregnancies complicated by hypertensive states of pregnancy.

Disqualifiers

Minors under 18 years of age.

Women with mental disabilities.

Major congenital fetal anomaly.

Trial population

Pregnant patients undergoing regular hospital follow-up

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

50 Participants
are grouped into 1 trial group
Group A: • Duration of gestation in pregnancy complicated by hypertensive state of pregnancy with antihyperte

Trial outcomes

Primary outcomes

1

Prolongation of at least one week of gestation in pregnancy complicated by hypertensive state of pregnancy with antihypertensive therapy guided by hemodynamic phenotypes

Number of weeks of pregnancy

Time frame
Up to 40 weeks

Secondary outcomes

Other outcomes

Sponsors and contacts

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