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Recruiting NCT06720363

NCT06720363 Development of a Predictive Model of Fetal PH At Birth from Novel Variables Derived from Cardiotocographic Tracing

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Clinical Trial Summary
NCT ID NCT06720363
Status Recruiting
Phase
Sponsor IRCCS Azienda Ospedaliero-Universitaria di Bologna
Condition Pregnancies At Increased Risk of Preterm Birth
Study Type OBSERVATIONAL
Enrollment 5,000 participants
Start Date 2024-06-07
Primary Completion 2028-06-01

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age 45 Years
Study Type OBSERVATIONAL

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.

This trial targets 5,000 participants in total. It began in 2024-06-07 with a primary completion date of 2028-06-01.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

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.

Eligibility Criteria

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

Contact & Investigator

Central Contact

Antonio Farina, MD

✉ antonio.farina@unibo.it

📞 0512143110

Principal Investigator

Antonio Farina, MD

PRINCIPAL INVESTIGATOR

IRCCS Azienda Ospedaliero-Universitaria di Bologna

Frequently Asked Questions

Who can join the NCT06720363 clinical trial?

This trial is open to female participants only, aged 18 Years or older, up to 45 Years, studying Pregnancies At Increased Risk of Preterm Birth. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT06720363 currently recruiting?

Yes, NCT06720363 is actively recruiting participants. Contact the research team at antonio.farina@unibo.it for enrollment information.

Where is the NCT06720363 trial being conducted?

This trial is being conducted at Bologna, Italy.

Who is sponsoring the NCT06720363 clinical trial?

NCT06720363 is sponsored by IRCCS Azienda Ospedaliero-Universitaria di Bologna. The principal investigator is Antonio Farina, MD at IRCCS Azienda Ospedaliero-Universitaria di Bologna. The trial plans to enroll 5,000 participants.

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