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NCT02741531 · ClinicalTrials.gov registry record · NA
The Effect of Partial Bladder Filling on Post-operative Time to Void in Minimally Invasive Gynecologic Procedures
A NA study of Hysterectomy and Myomectomy, sponsored by George Washington University.
- Completed
- Registry status
- NA
- Development phase
- 100
- Enrollment target
- 1
- Study location
NCT02741531: Completed NA study of Hysterectomy and Myomectomy, sponsored by George Washington University.
NCT02741531 is a NA study of Hysterectomy and Myomectomy that has completed, run by George Washington University. The registered enrollment target is 100 participants, below the 127-participant average among 8 other Hysterectomy trials with a reported enrollment target (21% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02741531, a NA study of Hysterectomy and Myomectomy, has completed, sponsored by George Washington University.
- COMPLETED
- Registry status
- NA
- Development phase
- 100 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to determine if partially filling the bladder after laparoscopic/robotic gynecologic surgery (for benign disease) shortens the time required to spontaneously void for patients to determine if this subsequently shortens patient stay times in the Post Anesthesia Care Unit (PACU) following surgery. This intervention would be compared to the current standard of care, which involves removing the patient's Foley catheter with an empty bladder and then giving the patient up to 6 hours to void in the PACU.
Primary Outcome
the time (in minutes) between when the patient's foley is removed and when the patient is able to void in the PACU.
Conditions Studied
Interventions
- OTHER saline solution
- OTHER Bladder filled with saline solution
Study Locations (1)
District of Columbia
- George Washington University Medical Faculty Associates - Washington D.C.
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 100 participants |
| Start Date | 2016-03 |
| Est. Completion | 2017-07-27 |
| Phase | NA |
What the finished NCT02741531 record still lists
NCT02741531 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 127-participant average among 8 other Hysterectomy trials with a reported enrollment target (21% lower).
The record links to 2 conditions, with Hysterectomy appearing as the primary indexed condition, and to 2 interventions - of which saline solution is the first listed.
NCT02741531 reports a single indexed study location in District of Columbia.
Frequently Asked Questions
What is clinical trial NCT02741531 about?
NCT02741531 is a clinical study titled "The Effect of Partial Bladder Filling on Post-operative Time to Void in Minimally Invasive Gynecologic Procedures". The purpose of this study is to determine if partially filling the bladder after laparoscopic/robotic gynecologic surgery (for benign disease) shortens the time required to spontaneously void for patients to determine if this subsequently shortens patient stay times in the Post Anesthesia Care Unit ...
What is the current status of trial NCT02741531?
This trial is currently completed. It is a NA study. The enrollment target is 100 participants. The study started on 2016-03. Estimated completion is 2017-07-27.
What conditions does trial NCT02741531 study?
This clinical trial studies the following conditions: Hysterectomy, Myomectomy.
What interventions are being tested in trial NCT02741531?
The interventions under investigation include: saline solution (OTHER), Bladder filled with saline solution (OTHER).
Who is sponsoring clinical trial NCT02741531?
This trial is sponsored by George Washington University, which has 133 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT02741531 being conducted?
This trial has 1 study location across District of Columbia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Hysterectomy
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT02741531's enrollment target sits among peer trials
100 4th of 8 higher than 4 of 8 other Hysterectomy trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Hysterectomy trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
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