Feasibility Study of NERv's Inline Device for Postoperative Complications
Unknown Phase 2 NCT04582708
Study Description
Using NERv's Inline Device to Monitor Surgical Recovery and Detect Complications
Study Details
- Registry ID:
- NCT04582708
- Conditions:
- Anastomotic Leak, Fistula, Postoperative Leak, Postoperative Pancreatic Fistula, POPF
- Phase:
- Phase 2
- Target Enrollment:
- 316 participants
- Start Date:
- Age Range:
- 18–999 years
- Healthy Volunteers:
- No
Study Locations (9 sites)
-
King Saud University Medical City
Riyadh, Saudi Arabia -
King Saud University Medical City
Riyadh, Riyadh Province, Saudi Arabia -
St. Michael's Hospital
Toronto, Ontario, Canada -
St. Joseph's Health Centre
Toronto, Ontario, Canada -
Juravinski Hospital- Hamilton Health Sciences
Hamilton, Ontrario, Canada -
Hamilton General Hospital
Hamilton, Ontario, Canada -
Juravinski Hospital- Hamilton Health Sciences
Hamilton, Ontario, Canada -
Grand River Hospital
Kitchener, Ontario, Canada -
Cleveland Clinic
Cleveland, Ohio, United States
Interested in Participating?
Check your eligibility and learn more about this study on TrialScreen.