Modified Myocardial Performance Index and Epicardial Thickness in Cases With Idiopathic Polyhydramnios

NCT ID: NCT05737043

Last Updated: 2023-02-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

90 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-07-22

Study Completion Date

2023-02-12

Brief Summary

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In cases diagnosed as idiopathic polyhydramnios and healthy pregnancy between 24-40 weeks (total number of cases (100-120)), prospective fetal echocardiography will be performed to evaluate MPI and EFT.

Detailed Description

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: gestational week, maternal age, amniotic fluid index measurement, modified myocardial performance in fetal echo and epicardial thickness of all cases will be evaluated. week of pregnancy, body mass index, fetal biometry, umbilical artery doppler, middle cerebral artery doppler measurements will be taken. Birth weight and fetal intensive care hospitalizations at the birth week of all cases will be recorded. All data will be evaluated with the appropriate statistical method.

Conditions

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Fetal Diagnose Fetal Cardiac Disorder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

SEQUENTIAL

Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

DOUBLE

Caregivers Investigators

Study Groups

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myocardial performance and epicard thickness in case with polyhidramnios

we will do a fetal echo, and fetal screening with ultrasonography

Group Type PLACEBO_COMPARATOR

prenatal diagnose

Intervention Type DIAGNOSTIC_TEST

we will do a fetal echo in pregnant women with polyhidramnios

pregnant women with polyhidramios

Group Type ACTIVE_COMPARATOR

prenatal diagnose

Intervention Type DIAGNOSTIC_TEST

we will do a fetal echo in pregnant women with polyhidramnios

Interventions

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prenatal diagnose

we will do a fetal echo in pregnant women with polyhidramnios

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Exclusion Criteria

\-
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

Yes

Sponsors

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Necmettin Erbakan University

OTHER

Sponsor Role lead

Responsible Party

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şükran doğru

md

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Necmettin Erbakan University

Konya, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

Other Identifiers

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2023/4145(10675: neu)

Identifier Type: -

Identifier Source: org_study_id

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