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Ultrasound to Investigate Tip Dislodgment of Epicutaneous-caval Catheter.

NCT06438289 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 217

Last updated 2025-02-28

No results posted yet for this study

Summary

This is a non-pharmacological, non-profit, prospective, observational multicenter study. Primarily, the study aims to demonstrate the feasibility of ultrasound methodology to study the secondary malposition of epicutaneous-caval catheters (ECC) in neonates.

After obtaining informed consent, the study involves performing ultrasound tip location on newborns who had an ECC placed. This will occur immediately after the placement and, if in a central position, subsequently at 60-120 minutes, 48-72 hours and 6-8 days post-placement. Data will be collected on various variables. Each Center will contribute at least 20 cases to the cohort and all data will be recorded in a database. The study is expected to last for 12 months

Conditions

  • Migration of Implant or Internal Device

Sponsors & Collaborators

  • Federico II University

    lead OTHER

Eligibility

Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-01-17
Primary Completion
2024-10-15
Completion
2024-10-15

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06438289 on ClinicalTrials.gov