Clin2
NCT06263075Likely a fitRecruiting

Monitoring during craniosynostosis surgery: comparing newer vs. traditional monitors

CraniosynostosesHypovolemiaHemorrhageHemodynamic Instability

Part of Bones, joints & muscles, Genetic & congenital clinical trials.

This study compares two types of monitors that track your baby's heart and blood flow during surgery to fix craniosynostosis. The goal is to see if a newer monitor works as well as the traditional one.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
30 people
Ages
3 months to 8 months
Study type
Observational

Who can take part

  • Your baby must be between 3 and 8 months old.
  • Your baby has been diagnosed with craniosynostosis and is scheduled for corrective surgery.
  • Your baby should not have heart problems, metabolic diseases, or be born before 30 weeks.
  • Your baby must weigh at least 3 kg (about 6.6 pounds).
  • The medical monitors used during surgery must be working correctly and not blocked or dislocated.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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