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Development of a Predictive Model of Fetal PH At Birth from Novel Variables Derived from Cardiotocographic Tracing

Development of a Predictive Model of Fetal PH At Birth from Novel Variables Derived from Cardiotocographic Tracing

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06720363
Enrollment
5000
Registered
2024-12-06
Start date
2024-06-07
Completion date
2028-08-01
Last updated
2024-12-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancies At Increased Risk of Preterm Birth

Keywords

Fetal acidosis, pH, cardiotocography, CTG

Brief summary

The goal of this observational study is to build a predictive model of fetal acidosis based on variables from the cardiotocographic tracing recorded during labor in participants undergoing spontaneous or induced delivery with single pregnancy.

Detailed description

Cardiotocography is the current tool used to assess fetal well-being in labor and to identify cases of fetal distress early. We decided to conduct this study because the current interpretation of the cardiotocographic trace has limitations, related to the subjective interpretation of the trace. There are currently no predictive models that can reduce this margin of error. Creating a predictive model of fetal acidosis, based on variables from the cardiotocographic tracing, could be useful in order to enable a better and more timely intervention. It can also be useful in reducing the rate of improper obstetric interventions. The recording of the cardiotocographic trace will take place throughout the duration of labor as per internal clinical management recommendations. Once delivery has taken place (by cesarean section, obstetric suction or spontaneously), the data derived from the cardiotocographic tracing will be extracted using the Sonicaid Fetal Care Software from the cardiotocograph into a .csv file that will report for each second four measurements of heart rate and intensity of maternal contractions. The .csv file is converted to a .sav file and the new variables are generated, using a specially created SPSS script, in order to calculate the stability and variability of fetal heart rate. Neonatal outcomes will be considered the dependent variable in this set of variables originated from the fetal heart rate patterns. The clinical variables that will be collected for the predictive model and/or for descriptive purposes are: * umbilical artery and vein pH * excess umbilical artery and vein bases * Apgar score at birth * presence of dyed amniotic fluid * onset of active labor of delivery * onset of the expulsive period * fetal expulsion * cord rounds * mode of delivery * neonatal weight.

Interventions

None listed

Sponsors

IRCCS Azienda Ospedaliero-Universitaria di Bologna
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
No

Inclusion criteria

* Maternal age between 18 and 45 years; * Single pregnancy * Participants undergoing continuous monitoring of labor labor * Obtaining informed consent for study participation and processing of personal data

Exclusion criteria

* None

Design outcomes

Primary

MeasureTime frameDescription
Fetal acidosisDuring deliverypH value ≤ 7.10

Countries

Italy

Contacts

Primary ContactAntonio Farina, MD
antonio.farina@unibo.it0512143110

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026