Development and Evaluation of iPleth for Uganda (in vivo evaluation)
TTo evaluate the usability of the iPleth interface pulse oximeter prototype in the hands of expert anesthesiologists/trainees, anesthesia technicians, nurses and lay medical users to determine areas for improvement for the interface.
Who can participate in this study?
- Anyone having surgery.
Who should not participate in this study?
- Subjects that do not consent or who are unable to consent cannot participate in this study.
Status?
- Preparing to start recruitment.
For more information, please see the Consent/Information form