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Recruiting NCT07305519

NCT07305519 The Combined Effect of Magnesium, Palmitoylethanolamide, High-Molecular-weight Hyaluronic Acid, Vitamin B6, and Vitamin D in Preventing Preterm Birth:

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Clinical Trial Summary
NCT ID NCT07305519
Status Recruiting
Phase —
Sponsor University of Roma La Sapienza
Condition Preterm Labor
Study Type INTERVENTIONAL
Enrollment 150 participants
Start Date 2026-04-01
Primary Completion 2027-04-01

Eligibility & Interventions

Sex Female only
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Magnesium-PEA-HMW Hyaluronic Acid-Vitamin B6-Vitamin D + Vaginal ProgesteroneStandard Treatment (Guideline-Based)

Eligibility Fast-Check

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

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 150 participants in total. It began in 2026-04-01 with a primary completion date of 2027-04-01.

⚠ 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 aim of the study is to assess the effect of a combination of Magnesium, Palmitoylethanolamide, high-molecular-weight Hyaluronic Acid, Vitamin B6, and Vitamin D in women at risk of preterm birth (PTB).

Eligibility Criteria

Inclusion Criteria: * Signed informed consent Singleton pregnancy Maternal age ≥ 18 years Gestational age between 20+0 and 34+0 weeks at enrollment Cervical length between 15 mm and 30 mm measured by transvaginal ultrasound Exclusion Criteria: * Fetal structural anomalies Maternal chronic diseases or pregnancy-related conditions, including diabetes, hypertension, preeclampsia, cardiovascular disease, infections, or autoimmune disorders Multiple gestation Fetal growth abnormalities (estimated fetal weight \<10th or \>90th percentile) Prelabor rupture of membranes (PROM)

Contact & Investigator

Central Contact

Giuseppe RIZZO, Professor

✉ giuseppe.rizzo@uniroma1.it

📞 +393386973001

Frequently Asked Questions

Who can join the NCT07305519 clinical trial?

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

Is NCT07305519 currently recruiting?

Yes, NCT07305519 is actively recruiting participants. Contact the research team at giuseppe.rizzo@uniroma1.it for enrollment information.

Where is the NCT07305519 trial being conducted?

This trial is being conducted at Rome, Italy.

Who is sponsoring the NCT07305519 clinical trial?

NCT07305519 is sponsored by University of Roma La Sapienza. The trial plans to enroll 150 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: November 2026  ·  Data Methodology