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Clinical Trial Summary

This is a study to evaluate whether use of a pedometer following radical prostatectomy decreases post-operative narcotic use and time to return of bowel function.


Clinical Trial Description

This is a randomized controlled prospective study looking at the effect of using a pedometer with graduated step-count goals following radical prostatectomy on return of bowel function and post-operative narcotic use. Subjects will be randomized into a control group or study group. The control group will receive standard of care, with information provided regarding the importance of ambulation following surgery. The study group will receive a pedometer with graduated step-count goals from post-operative day 0 to post-operative day 14. Both groups will be given a standardized post-operative narcotic regimen, and will be asked to record initial passage of flatus and first bowel movement. Subjects will remain on the study until initial post-operative visit. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04206280
Study type Interventional
Source Benaroya Research Institute
Contact Basil Ferenczi, MD
Phone 206-223-6600
Email basil.ferenczi@virginiamason.org
Status Recruiting
Phase N/A
Start date February 10, 2020
Completion date February 2021

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