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Clinical Validation of Suntech Advantage MX With Suntech Neonate and Children Cuff Line

NCT06172829 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2024-03-05

No results posted yet for this study

Summary

Patients will be selected according to specific criteria. Upon selection, patients with an existing intra-arterial line will have their blood pressure monitored with the SunTech Advantage MX module in addition to the reference data collected from intra-arterial line. Data collected from the Advantage MX module will be compared to the reference data from the intra-arterial line.

Conditions

Interventions

DEVICE

Advantage MX Module

no intervention will be provided.

Sponsors & Collaborators

Eligibility

Min Age
1 Month
Max Age
3 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-11-07
Primary Completion
2024-03-01
Completion
2024-03-01
FDA Device
Yes

Countries

  • United States

Study Locations

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Entities

Diseases
Companies

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 NCT06172829 on ClinicalTrials.gov