Development and Evaluation of iPleth for Uganda (in vivo evaluation)

To 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?

• Consenting anesthesiologists, anesthesia residents, anesthesia technicians, nurses, engineers and lay users may participate in this study.

Who should not participate in this study?

• Subjects that do not consent or who are unable to consent cannot participate in this study.

Status?

• Only recruiting staff anesthesiologists, anesthesia residents, anesthesia technicians, nurses, engineers at our target institutions.

For more information, please see the Consent/Information form