Recruiting

Assessment Intravenous Site Events During Outpatient Infusion Procedures With a Wireless Thermal Measurement Device During

Rhaeos, Inc. · NCT07009405

Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.

Key facts

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This study evaluates a Non-invasive Thermal Infusion Site Monitor (NTISM) device when used during routine outpatient infusion treatments.

Being studied: non-invasive thermal infusion site monitoring NTISM device

Conditions: IV Infiltration; IV Extravasation

Copied from the official record. The study team makes the final decision at screening.

Show full criteria

Inclusion Criteria

Scheduled to receive an infusion therapy of at least 30 minutes in length
Region of intact skin proximal to the infusion catheter insertion site that is appropriate in size for application of the study device
Signed informed consent
Available for 15 minutes of post-measurement monitoring following removal of the study device

Exclusion Criteria

Patient is under 12 years of age
Patient-reported history of serious adverse skin reactions to silicone-based adhesives or Tegaderm
Use of the study device would interfere with standard patient care that cannot be delayed, or participation in the study will interfere with, or be detrimental to, administration of optimal healthcare to the subject
Investigator judges that the intravenous