Clinical Trials Directory

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UnknownNCT02821988

Antenatal Testing in Obese Woman, is it Really Necessary?

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
University of Tennessee · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

It is well established that obese women are at an increased risk of stillbirth compared to non obese women. This has led many physicians to begin antenatal testing in obese women in the third trimester through either nonstress tests or biophysical profiles. However, there is little evidence that antenatal testing improves fetal outcomes in obese women. The aim of this study is to determine if antenatal testing improves outcomes in obese women and to determine the optimal mode of testing (either nonstress tests or biophysical profiles).

Detailed description

1. Purpose: To determine if antenatal testing improves outcomes in obese pregnant women 2. Rationale: It has been well established that obese pregnant women are at increase risk of stillbirth compared to matched non obese controls. This relative risk is increased not only with increasing gestational age in obese women but with increasing severity of obesity. The increased risk of stillbirth has led some obstetricians to begin antenatal testing in obese women; however, there is little evidence that antenatal fetal surveillance improves outcomes. 3. Study/Project Population: Pregnant women before 32 weeks of gestation with an initial BMI \>30kg/m2 4. Research Design: Randomized Controlled Trial 5. Study/Project Procedures: Patients will be randomized to one of three groups: daily kick counts only, nonstress test, amniotic fluid index, and daily kick counts, and biophysical profile and daily kick counts. These patients will be randomly assigned a group in a 1:1:1 ratio using a random number generator available online. Patients assigned to the daily kick counts only group will be called weekly to ensure they are doing daily kick counts. If they are noncompliant, they will be removed from the study and will undergo nonstress tests if they meet the initial BMI criteria as is the standard practice at our institution. 6. Outcomes Measured: Stillbirth, induction of labor, mode of delivery, neonatal intensive care unit admission, AGPARs \<7 at 5 minutes of life

Conditions

Interventions

TypeNameDescription
DEVICEExternal fetal monitor for Nonstress test
DEVICEUltrasonography for Biophysical profile

Timeline

Start date
2016-07-01
Primary completion
2017-05-01
Completion
2017-05-01
First posted
2016-07-04
Last updated
2016-07-04

Source: ClinicalTrials.gov record NCT02821988. Inclusion in this directory is not an endorsement.