Clinical trial Recruiting at 1 site Interventional Women only

Determining the best time to measure cervical length during fetal anatomy surveys

Official title: Optimal Timing of Routine Cervical Length Measurements During Anatomy Survey

Run by Henry Ford Health System · NCT06822647 · Data updated 2026-11-12

This study is testing the best time to measure cervical length during ultrasounds in pregnant people to see if it makes a difference in accuracy, while also comparing two types of ultrasound images.

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Quick facts

Study typeInterventional
SexWomen only
Enrollment550 (estimated)
SponsorHenry Ford Health System
Academic / other
Locations1 site (Detroit, Michigan)
StatusRecruiting
StartedJanuary 20, 2025
Main results expectedJune 1, 2027
Study endsJuly 1, 2027
Registry record updatedMarch 9, 2026
Trial IDNCT06822647 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal candidates are pregnant individuals between 16 weeks and 23 weeks + 6 days of gestation presenting for a fetal anatomy survey at Henry Ford Health.

Probably not a fit

Patients with a history of preterm delivery or cervical insufficiency will not benefit from this study.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This clinical trial aims to identify the optimal timing for cervical length measurements during fetal anatomy surveys in pregnant individuals. It compares measurements taken at the beginning versus the end of the ultrasound exam to see which timing yields more accurate results. Additionally, the study evaluates the effectiveness of sepia-filtered ultrasound images against conventional grayscale images in meeting established accuracy criteria. Participants will be randomized into two groups for cervical length measurement and will undergo both imaging techniques.

Why it matters

Potential benefit: If successful, this study could enhance the accuracy of cervical length assessments, potentially reducing the risk of preterm birth.

How similar studies have gone: While this approach is novel in its specific focus on timing and imaging techniques, similar studies have shown the importance of accurate cervical length measurement in predicting preterm birth.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Pregnant individuals between 16 weeks and 23 weeks + 6 days of gestation.
* Presenting for a fetal anatomy survey at Henry Ford Health MFM ultrasound units.
* Consent to a transvaginal cervical length measurement as part of routine care.
* Agreement to participate in the study, including randomization for the timing of cervical length measurement.

Exclusion Criteria:

* History of preterm delivery.
* Diagnosis of cervical insufficiency.
* Declines or unable to consent to a transvaginal cervical length measurement.
* Patients receiving care at non-Henry Ford Health radiology clinics.

Where it's running

  • Henry Ford Health New Center One
    Detroit, Michigan, United States
    Recruiting

Study contacts

  • Principal investigator: Raminder Khangura, MD — Henry Ford Health
  • Study coordinator: Shelby A Masters, MD
  • Email: smaster1@hfhs.org
  • Phone: 313-671-5225

Similar studies

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.