N/A
N=104
Spontaneous Void Requirements for Patients Undergoing Ambulatory Anorectal Surgery
Complications, Postoperative
Bottom Line
View on ClinicalTrials.gov: NCT03812536 ↗Enrolled (actual)
104
Serious AEs
0.0%
Results posted
Mar 2025
Primary outcome: Primary: PACU Time — 129.1; 210.0 Minutes
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- No Void (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Syed Husain
- Primary completion
- Aug 2020
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY PACU Time |
129.1; 210.0 | — |
| SECONDARY 30-day Readmission |
0; 0 | — |
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.
Eligibility Criteria
Inclusion Criteria
- Age 18-80 years old
- Patients undergoing hemorrhoidectomy, fistulotomy or anal condyloma excision
Exclusion Criteria
- Age 80 yo
- Prisoners
- Pregnant Women
- Unable or unwilling to follow the study protocol or any reason the research team believes the subject is not appropriate candidate for this study
Data sourced from ClinicalTrials.gov (NCT03812536). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.