N/A
N=60
Evaluation of Capillary Refill Index
Perfusion; Complications
Bottom Line
View on ClinicalTrials.gov: NCT04144166 ↗Enrolled (actual)
60
Serious AEs
0.0%
Results posted
Feb 2021
Primary outcome: Primary: Predictive Capability of the Altered Peripheral Perfusion — 0.89; 1.00; 0.94; 0.82 probability
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- capillary refill index (CRI) (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Nihon Kohden
- Primary completion
- Dec 2019
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Predictive Capability of the Altered Peripheral Perfusion |
0.89; 1.00; 0.94; 0.82; 0.986; 0.910 | — |
| SECONDARY Correlation of Device CRI to Conventional (Visual) CRT |
0.866 | — |
Summary
Comparison of a peripheral perfusion assessment method using a pulse oximeter to the conventional capillary refill time visually assessed by a clinician.
Eligibility Criteria
Inclusion Criteria
- Individuals 18 years of age or older
- Patients who present to the ED or who are admitted to the ICU of North Shore University Hospital (NSUH)
Exclusion Criteria
- Pregnant
- Prisoners
- Finger, hand or forearm anatomical anomaly or disease that may interfere with attaching a pulse oximeter sensor
- Patients' deemed clinically unstable by the clinical team
Data sourced from ClinicalTrials.gov (NCT04144166). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.