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临床试验/NCT02821988
NCT02821988Unknown不适用

Antenatal Testing in Obese Woman, is it Really Necessary?

University of Tennessee0 个研究点目标入组 100 人开始时间: 2016年7月最近更新:
适应症

试验速览

阶段
不适用
入组人数
100
主要终点
Stillbirth

研究概览

简要总结

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).

详细描述

  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

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • less then 32 weeks gestation BMI > 30kg/m2 English speaking

排除标准

  • age < 18 age >45 medical comorbidity which requires antenatal testing other than obesity unwilling to consent Non-English speaking not pregnant Gestational age >32 weeks

结局指标

主要结局

Stillbirth

时间窗: until delivery, up to 41 weeks

demise of infant prior to delivery as verified by ultrasonography

Mode of delivery

时间窗: at delivery, up to 41 weeks

whether the subject undergoes a vaginal delivery, cesarean delivery, or operative delivery will be recorded

次要结局

  • Apgar score of less than 7 at 5 minutes(at delivery, up to 41 weeks)
  • Neonatal intensive care unit admission admission(at delivery, up to 41 weeks)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Laura Grese

MD

University of Tennessee

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