se of a smartphone camera to assess pupil response to light in neurocritical care – comparison with pen torch
Phase 3
Completed
- Conditions
- Critically ill patients admitted to neurocritical careNot Applicable
- Registration Number
- ISRCTN53630869
- Lead Sponsor
- Solvemed Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Any patient admitted to neurocritical care
Exclusion Criteria
Pupillary assessment not possible due to ocular pathology
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pupil diameter (millimetres) and pupil reactivity (binary – responsive or non-responsive) measured using the two modalities (pentorch and Solvemed smartphone application), performed hourly during the day shift, for a maximum of 10 days per patient
- Secondary Outcome Measures
Name Time Method There are no secondary outcome measures