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NCT03857659 · ClinicalTrials.gov registry record · NA
Serial Third Trimester Abdominal Circumference and Amniotic Fluid Measurements Versus Routine Care
A NA study, sponsored by The University of Texas Health Science Center, Houston.
- Terminated
- Registry status
- NA
- Development phase
- 113
- Enrollment target
NCT03857659: Clinical Trial NA study, sponsored by The University of Texas Health Science Center, Houston.
NCT03857659 is a NA study that was terminated before completion, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 113 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT03857659, a NA study, was terminated before completion, sponsored by The University of Texas Health Science Center, Houston.
- TERMINATED
- Registry status
- NA
- Development phase
- 113 participants
- Enrollment target
Study Summary
The purpose of this study us to compare the rate of prenatal identification of abnormal fetal growth or amniotic fluid between clinical evaluation of uterine size by symphysis fundal height (SFH) measurements versus point-of-care ultrasound (POC-US) evaluation of abdominal circumference (AC) and maximum vertical pocket (MVP).
Primary Outcome
Abnormal fetal growth or amniotic fluid as assessed by clinical evaluation of uterine size by SFH versus POC-US evaluation.
Interventions
- DIAGNOSTIC_TEST Point-of-care ultrasound (POC-US)
- DIAGNOSTIC_TEST Routine antenatal care
- DIAGNOSTIC_TEST Formal ultrasound
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 113 participants |
| Start Date | 2019-04-05 |
| Est. Completion | 2020-05-20 |
| Phase | NA |
Why NCT03857659 stopped before completion
NCT03857659 is an interventional study that assigns participants to a tested intervention. The registered 113 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).
The record links to 0 conditions, and to 3 interventions - of which Point-of-care ultrasound (POC-US) is the first listed.
NCT03857659 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT03857659 about?
NCT03857659 is a clinical study titled "Serial Third Trimester Abdominal Circumference and Amniotic Fluid Measurements Versus Routine Care". The purpose of this study us to compare the rate of prenatal identification of abnormal fetal growth or amniotic fluid between clinical evaluation of uterine size by symphysis fundal height (SFH) measurements versus point-of-care ultrasound (POC-US) evaluation of abdominal circumference (AC) and max...
What is the current status of trial NCT03857659?
This trial is currently terminated. It is a NA study. The enrollment target is 113 participants. The study started on 2019-04-05. Estimated completion is 2020-05-20.
What interventions are being tested in trial NCT03857659?
The interventions under investigation include: Point-of-care ultrasound (POC-US) (DIAGNOSTIC_TEST), Routine antenatal care (DIAGNOSTIC_TEST), Formal ultrasound (DIAGNOSTIC_TEST).
Who is sponsoring clinical trial NCT03857659?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT03857659's enrollment target sits among peer trials
113 813th of 2000 higher than 1,188 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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