Development of Italian Fetal Growth Charts - Join Clinical Trial NCTNCT05774912
How to Join This Clinical Trial - NCTNCT05774912
Learn how to participate in this clinical trial studying an investigational therapy for Growth Charts. This study is currently enrolling participants.
Am I Eligible for This Clinical Trial?
This clinical research study is looking for participants with Growth Charts. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.
- Condition Being Studied
- Growth Charts
- Treatment Being Tested
- Investigational treatment
- Study Phase
- Clinical trial phase - Research study
- Enrollment Status
- Currently enrolling participants
- Study Identifier
- NCTNCT05774912 - ClinicalTrials.gov Identifier
- Sponsored By
- Study sponsor
What to Expect as a Participant
Participating in this clinical trial involves:
- Initial screening to determine eligibility
- Regular study visits and health assessments
- Receiving the study treatment or placebo
- Medical monitoring and follow-up care
- Contributing to medical research that may help others
- Potential access to new treatments before they're widely available
Clinical Trial Benefits and Compensation
Participants in this clinical research study may receive:
- Close medical monitoring by healthcare professionals
- Access to potential new treatments
- Compensation for time and travel (varies by study)
- No-cost study-related medical care
- The opportunity to help advance medical knowledge
Where Is This Clinical Trial Located?
This study is enrolling participants at 3 locations. Find a study site near you:
Clinical Research Site
Roma, Lazio 00168 - Italy
Status: NOT_YET_RECRUITING
Clinical Research Site
Milano, Lombardia 20122 - Italy
Status: NOT_YET_RECRUITING
Clinical Research Site
Trieste, 34137 - Italy
Status: RECRUITING
How to Enroll in This Study
To learn more about participating in this clinical trial for Growth Charts:
- Review the eligibility criteria with your healthcare provider
- Contact the study team for a pre-screening interview
- Schedule an in-person screening visit if eligible
- Review and sign the informed consent form
- Begin participation in the clinical trial
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