Motus GI believes that clinical research data is generated in many important avenues such as sponsored trials, investigator-initiated studies (IIS) and real-world evidence endeavors. Each avenue contributes in different ways and specifically, investigator-initiated research allows for industry and the medical community to pursue equally important ideas in a collaborative environment. The value of the scientific research produced by investigators, is key to complementing sponsored research and Motus GI is committed to supporting investigator led initiatives.
Motus GI defines an IIS as a clinical study conceptualized, developed and executed by an independent third-party sponsor. Each IIS must be unsolicited, and conducted without the participation of Motus GI and using the highest level of scientific rigor.
Pure-Vu EVS training and implementation process |
Comparison to standard-of-care
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Diagnostic yield—LGIB |
Impact on 30-day re-admit rates and bleeding recurrence rates |
Clinician satisfaction & usability |
Impact on bowel prep regimen |
Impact of Pure-Vu EVS on hospital efficiency
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Comparison to standard of care
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Use in patients that are high risk for IBP or poor visualization |
Pure-Vu use in CRC screening populations |
Use of Pure-Vu in vulnerable patients |
Impact of Pure-Vu on IBP related OC cancellation |
Pure-Vu training and implementation process |
Impact on bowel prep regimen |
Pure-Vu use with other technologies (AI or others) |
Clinician satisfaction & usability |