INFIL-6: IL6 on Umbilical Cord (Evaluation of IL-6 Levels on Umbilical Cord)

Sponsor
Parma University Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05793970
Collaborator
(none)
450
2
14.2
225
15.8

Study Details

Study Description

Brief Summary

Fetal inflammatory response syndrome (FIRS) is a major cause of non-hypoxic fetal intrapartum injury. One of the most common determinants of FIRS during labor is the exposure to an ongoing intra-amniotic infectious agent as in the event of a chorioamnionitis. Interleuchine-6 (IL-6) is considered a reliable hallmark of FIRS. No specific fetal heart rate pattern for the diagnosis of FIRS have been described so far at intrapartum Cardiotocography (CTG). The aim the present study is to investigate the correlation between intrapartum CTG findings and IL-6 levels on the arterial cord.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The labor will be managed according to the local protocol and 5mL of blood will collected from the umbilical artery soon after birth to determine the IL-6 values. CardioTocography (CTG) traces will be retrospectively reviewed by two expert operators that will be blinded to the IL-6 results and will categorize them as "inflammatory" or "not inflammatory".

    Inflammatory pattern will be defined in presence of 1) inappropriately high FHR for the given gestational age and/or 2) an increase >10% compared with the FHR baseline values at admission without preceding deceleration with/without reduced variability or absent cycling.

    The association between CTG findings as the umbilical levels of IL6 will be analyzed.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    450 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    Evaluation of IL-6 Levels on Umbilical Cord
    Actual Study Start Date :
    Mar 25, 2022
    Anticipated Primary Completion Date :
    Mar 23, 2023
    Anticipated Study Completion Date :
    Jun 1, 2023

    Outcome Measures

    Primary Outcome Measures

    1. IL6 Levels [IL6 will be measured on the umbilical blood sampled within 5 minutes after birth]

      correlation between intrapartum CTG findings and IL-6 levels on the arterial cord

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 50 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • singleton pregnancies at term submitted to a continuous CTG tracing during labor

    Exclusion Criteria:elective Cesarean Delivery, maternal tachycardia or pyrexia >38°C, drugs assumption

    -

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University Hospital of Parma Parma Italy 43123
    2 Fondazione Universitaria Policlinico Gemelli Roma Italy 00186

    Sponsors and Collaborators

    • Parma University Hospital

    Investigators

    • Principal Investigator: Tullio Ghi, Professor, University of Parma

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Tullio Ghi, Full Professor, Parma University Hospital
    ClinicalTrials.gov Identifier:
    NCT05793970
    Other Study ID Numbers:
    • 561/2021/OSS/AOUPR
    First Posted:
    Mar 31, 2023
    Last Update Posted:
    Mar 31, 2023
    Last Verified:
    Mar 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    Undecided
    Plan to Share IPD:
    Undecided
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 31, 2023