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.
Quick facts
| Study type | Interventional |
|---|---|
| Sex | Women only |
| Enrollment | 550 (estimated) |
| Sponsor | Henry Ford Health System Academic / other |
| Locations | 1 site (Detroit, Michigan) |
| Status | Recruiting |
| Started | January 20, 2025 |
| Main results expected | June 1, 2027 |
| Study ends | July 1, 2027 |
| Registry record updated | March 9, 2026 |
| Trial ID | NCT06822647 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
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Comparing laparoscopic and vaginal cerclage for preventing preterm birth
This study is testing whether a laparoscopic or vaginal stitch can better help women with weak cervixes prevent early births.
-
Predicting Adverse Pregnancy Outcomes in Uganda through Partnerships and Innovation
This study tests whether everyday health data, ultrasound, and blood samples from first-time pregnant women in Uganda can help predict problems like preeclampsia, fetal growth restriction, and preterm birth.
-
Cervical stiffness test to help predict preterm birth in at-risk pregnant women
A simple cervical stiffness test using the Pregnolia device is being studied to see if it can better identify women with threatened preterm labor who are likely to give birth soon.
-
Prenatal education to reduce environmental exposures during pregnancy
Aimed at pregnant people, this program tests whether a classroom-style education can help reduce exposure to harmful pollutants from seafood and nearby pollution sources.
-
How doctors and nurses decide about bed rest in pregnancy
This study tests a plan to stop routinely restricting activity or bed rest during pregnancy to see if providers accept it, find it appropriate, and change how often they recommend it for women at risk of preterm birth.
-
How cervical ultrasound settings affect AI prediction of preterm birth
This study tests whether an AI model for predicting preterm birth performs differently when cervical ultrasound images are taken with different imaging settings.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.