At a glance
ClinicalIndex Comparison RecordN/ACompleted· 104 enrolled
Drug / intervention
No Voidother
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Spontaneous Void Requirements for Patients Undergoing Ambulatory Anorectal Surgery
In Brief
A clinical study evaluating No Void for Complications, Postoperative. Completed, enrolled 104 participants across 1 site.
Detailed Summary
The objective of this study is to assess if not requiring patients to spontaneous void prior to discharge from the post-anesthesia care unit (PACU) will results in shorter lengths of stay in the post-anesthesia care unit without increasing hospital readmissions or emergency room visits.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsComplications, Postoperative
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20192020202120222023202420252026
Enrollment StartJun 2018
First PostedJan 2019
Primary CompletionAug 2020
TodayJul 2026
First PostedJan 23, 2019
Enrollment StartJun 19, 2018
Primary CompletionAug 7, 2020
TodayJul 2, 2026
Enrollment to primary: 2.1 yearsPosted 7.4 years ago
Interventions
No Voidother
Currently the protocol at The Ohio State University Hospital requires voiding spontaneously prior to discharge from the PACU. Our intervention group will be discharged home without having to void spontaneously as a discharge criteria.