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Alterations of the Uteroplacental and Fetal Pulmonary Circulation Following Amnioinfusion

NCT01258725 · Status: UNKNOWN · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2010-12-13

No results posted yet for this study

Summary

The aim of this study is to compare the uteroplacental and pulmonary circulation of the fetuses with severe (AFI\<5cm) idiopathic oligohydramnios (with unknown origin) to those in normal controls. Further purpose of the study is to measure the changes of the uteroplacental and fetal pulmonary circulation in patients presenting with severe idiopathic oligohydramnios, managed either with single amnioinfusion or with serial amnioinfusions.

Conditions

  • Severe Oligohydramnios

Interventions

PROCEDURE

amnioinfusion procedure

Single/serial amnioinfusions aimed at restoring amniotic fluid volume until a normal amount (AFI≥8cm).(Every pregnant women presenting with severe (AFI\<5) idiopathic (with unknown origin) oligohydramnios is treated with amnioinfusion at our Dept.)

Sponsors & Collaborators

  • Szeged University

    lead OTHER

Principal Investigators

  • János Sikovanyecz, M.D., Ph.D. · University of Szeged, Department of Obstetrics and Gynecology

  • Zoltan Kozinszky, M.D., Ph.D. · Department of Obstetrics and Gynecology, University of Szeged

Study Design

Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
49 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-01-31
Primary Completion
2011-09-30
Completion
2012-12-31

Countries

  • Hungary

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01258725 on ClinicalTrials.gov