NCT02008825 - Evaluation of the ViSiGiTM Calibration System | Biotech Hunter

Enrollment

Participants

Timeline

Start Date

January 31, 2014

Primary Completion Date

April 30, 2014

Study Completion Date

May 31, 2014

Conditions

Enhance Delineation of the Stomach Anatomy and the Surgeon's Appreciation of the Extent of Gastric Volume to be Removed;Increase the Safety Profile of the Patient (i.e., Reduce the Likelihood of Accidental Stapling of the Orogastric Tube or Bougie);Reduce the Incidence of OR Contamination/Infection Transmission;Streamline OR Workflow, Resulting in Reduced OR TimeEnsure Consistent and Reproducible Staple Lines.

Interventions

DEVICE

Utilization of ViSiGi calibration tube

DEVICE

Usual non suction Bougie

Trial Locations (1)

18104

Saint Luke's University and Health Network, Allentown