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NCT06822647 · ClinicalTrials.gov registry record · NA
Optimal Timing of Routine Cervical Length Measurements During Anatomy Survey
A NA study of Preterm Birth and Cervical Insufficiency, sponsored by Henry Ford Health System.
- Recruiting
- Registry status
- NA
- Development phase
- 550
- Enrollment target
- 1
- Study location
NCT06822647 is a NA study of Preterm Birth and Cervical Insufficiency that is actively recruiting participants, run by Henry Ford Health System. The registered enrollment target is 550 participants, below the 4,615-participant average among 37 other Preterm Birth trials with a reported enrollment target (88% lower). The trial reports 1 study location across 1 state.
The verdict
NCT06822647, a NA study of Preterm Birth and Cervical Insufficiency, is actively recruiting participants, sponsored by Henry Ford Health System.
- RECRUITING
- Registry status
- NA
- Development phase
- 550 participants
- Enrollment target
- 1
- Study location
Study Summary
The goal of this clinical trial is to determine the optimal timing for measuring cervical length (CL) during fetal anatomy surveys in pregnant individuals. This study focuses on improving the accuracy of cervical length assessments, which are critical for identifying individuals at risk for preterm birth. The main questions it aims to answer are: * Does measuring cervical length at the beginning of the anatomy survey result in a higher proportion of scans meeting the nine CLEAR (Cervical Length Education and Review) criteria compared to measuring at the end of the survey? * Does the use of sepia-filtered ultrasound images improve the proportion of scans meeting the nine CLEAR criteria compared to conventional grayscale images? Researchers will compare two groups of participants randomized to have cervical length measured either at the beginning or at the end of the anatomy survey. Additionally, all participants will undergo cervical length measurements using both grayscale and sepia-filtered ultrasound imaging. Participants will: * Receive a patient information sheet through MyChart explaining the study and standard cervical length screening during anatomy surveys. * Provide verbal consent for a transvaginal ultrasound and study participation. * Be randomized to have their cervical length measured at either the start or end of the fetal survey. * Undergo cervical length measurement using both grayscale and sepia-filtered ultrasound imaging modalities. * This study involves no additional risks beyond those of routine clinical care and aims to enhance clinical practice by identifying optimal methods for cervical length assessment during pregnancy.
Conditions Studied
Interventions
- PROCEDURE Cervical Length Measurement at the Beginning of the Anatomy Survey
- PROCEDURE Cervical Length Measurement at the End of the Anatomy Survey
Study Locations (1)
Michigan
- Henry Ford Health New Center One - Detroit
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 550 participants |
| Start Date | 2025-01-20 |
| Est. Completion | 2027-07-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06822647
The ClinicalTrials.gov registry entry for NCT06822647 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 550 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 4,615-participant average among 37 other Preterm Birth trials with a reported enrollment target (88% lower). The listed sponsor is Henry Ford Health System, which has 234 total studies on file at ClinicalTrials.gov.
The record links to 3 conditions, with Preterm Birth appearing as the primary indexed condition, and to 2 interventions - of which Cervical Length Measurement at the Beginning of the Anatomy Survey is the first listed.
NCT06822647 reports 1 study location spanning 1 distinct geographic area - top geographies include Michigan.
Frequently Asked Questions
What is clinical trial NCT06822647 about?
NCT06822647 is a clinical study titled "Optimal Timing of Routine Cervical Length Measurements During Anatomy Survey". The goal of this clinical trial is to determine the optimal timing for measuring cervical length (CL) during fetal anatomy surveys in pregnant individuals. This study focuses on improving the accuracy of cervical length assessments, which are critical for identifying individuals at risk for preterm ...
What is the current status of trial NCT06822647?
This trial is currently recruiting. It is a NA study. The enrollment target is 550 participants. The study started on 2025-01-20. Estimated completion is 2027-07-01.
What conditions does trial NCT06822647 study?
This clinical trial studies the following conditions: Preterm Birth, Cervical Insufficiency, Cervical Length Measurement.
What interventions are being tested in trial NCT06822647?
The interventions under investigation include: Cervical Length Measurement at the Beginning of the Anatomy Survey (PROCEDURE), Cervical Length Measurement at the End of the Anatomy Survey (PROCEDURE).
Who is sponsoring clinical trial NCT06822647?
This trial is sponsored by Henry Ford Health System, which has 234 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06822647 being conducted?
This trial has 1 study location across Michigan. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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