CM: Cervix Monitor for Detection Conditions Leading to Spontaneous Preterm Delivery

Sponsor
Advanced Tactile Imaging, Inc. (Industry)
Overall Status
Enrolling by invitation
CT.gov ID
NCT04247555
Collaborator
Rutgers, The State University of New Jersey (Other), St. Luke's Hospital and Health Network, Pennsylvania (Other), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) (NIH)
270
2
26.9
135
5

Study Details

Study Description

Brief Summary

Preterm birth is a leading cause of neonatal mortality despite of numerous advances and intensive research in perinatal medicine. Almost one million children die every year due to the complications of preterm birth and rates are on the rise. Of the 14 million survivors per year, most face a lifetime of disability, including learning disabilities, visual and hearing impairments. The majority of preterm birth happen spontaneously (SPTD) which is often a multi factorial event, precocious cervical softening, shortening and dilatation are a common underlying factor. In the scope of this project the investigators propose to develop and clinically validate a new device, Cervix Monitor (CM), for detecting cervix conditions leading to SPTD and its risk assessment.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    SPTD is closely related to a premature cervical ripening. The scientific basis for the proposed project is that the elasticity modulus of a cervix is a more sensitive parameter characterizing the stage of cervical ripening. The main component of the cervical tissue is collagen. Cervical ripening is the result of realignment of collagen, degradation of collagen cross-linking due to proteolytic enzymes. These processes affect the elasticity modulus of the cervical tissue. Therefore, assessment of cervix by a device (CM) measuring cervical elasticity (stiffness) and cervical length (effacement) appears to be an adequate approach for identifying pregnant women at high risk of SPTD. The CM is based on measuring applied pressure to the cervix by a tactile sensor array (stress data) and ultrasound measurement of cervix length (strain data). Tactile and ultrasound sensors are allocated on the tip of the measuring part of vaginal probe. The discovery of novel bio markers that could reliably identify women who will subsequently deliver preterm, may allow for timely medical intervention and targeted therapeutic treatments aimed at improving maternal and fetal outcomes.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    270 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    Cervix Monitor for Elasticity and Length Measurements
    Actual Study Start Date :
    Jan 3, 2020
    Anticipated Primary Completion Date :
    Mar 31, 2022
    Anticipated Study Completion Date :
    Mar 31, 2022

    Outcome Measures

    Primary Outcome Measures

    1. Cervix elasticity [During examination procedure]

      Units measurement of elasticity in kPa

    2. Cervix Length [During examination procedure]

      Units of measurement of length in mm

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    Female
    Inclusion Criteria:
    • Gestational age from 24 to 28 weeks at time of Cervix Monitor measurement

    • Singleton in the current pregnancy

    Exclusion Criteria:
    • Fatal anomaly

    • History of fetal reduction in the current pregnancy to the singleton gestation

    • Preterm rapture of membranes

    • Current or planned cervical cerclage

    • Planned indicated preterm delivery

    • Active known cancer of the colon, rectum wall, cervix, vaginal, uterus or bladder

    • Ischemic heart disease and or arrhythmia

    • Active skin infection or ulceration within the vaginal/vulva (Herpes infection)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Rutgers The State University Of New Jersey New Brunswick New Jersey United States 08854
    2 St. Luke's University Health Network Department of Obstetrics and Gynecology, Division of Maternal Fetal Medicine (MFM) Bethlehem Pennsylvania United States 18015

    Sponsors and Collaborators

    • Advanced Tactile Imaging, Inc.
    • Rutgers, The State University of New Jersey
    • St. Luke's Hospital and Health Network, Pennsylvania
    • Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    Investigators

    • Principal Investigator: Vladimir Egorov, PhD, Advanced Tactile Imaging, Inc.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Advanced Tactile Imaging, Inc.
    ClinicalTrials.gov Identifier:
    NCT04247555
    Other Study ID Numbers:
    • CM02
    • R44HD090793
    First Posted:
    Jan 30, 2020
    Last Update Posted:
    Jul 21, 2021
    Last Verified:
    Jul 1, 2021
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Product Manufactured in and Exported from the U.S.:
    Yes
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 21, 2021