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NCT03126162 · ClinicalTrials.gov registry record · NA
Postoperative Bladder Testing After Total Laparoscopic Hysterectomy
A NA study, sponsored by University of Pittsburgh.
- Completed
- Registry status
- NA
- Development phase
- 172
- Enrollment target
NCT03126162 is a NA study that has completed, run by University of Pittsburgh. The registered enrollment target is 172 participants.
The verdict
NCT03126162, a NA study, has completed, sponsored by University of Pittsburgh.
- COMPLETED
- Registry status
- NA
- Development phase
- 172 participants
- Enrollment target
Study Summary
The objective of this study is to determine if backfilling the bladder immediately post-operatively, prior to removal of the foley catheter, in patients undergoing same-day total laparoscopic hysterectomy will hasten time to first spontaneous void and time to discharge
Interventions
- PROCEDURE InstilIing normal saline into bladder
- PROCEDURE Removal of foley catheter
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 172 participants |
| Start Date | 2017-06-08 |
| Est. Completion | 2018-05-04 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03126162
The ClinicalTrials.gov registry entry for NCT03126162 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 172 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Pittsburgh, which has 1,238 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which InstilIing normal saline into bladder is the first listed.
NCT03126162 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT03126162 about?
NCT03126162 is a clinical study titled "Postoperative Bladder Testing After Total Laparoscopic Hysterectomy". The objective of this study is to determine if backfilling the bladder immediately post-operatively, prior to removal of the foley catheter, in patients undergoing same-day total laparoscopic hysterectomy will hasten time to first spontaneous void and time to discharge
What is the current status of trial NCT03126162?
This trial is currently completed. It is a NA study. The enrollment target is 172 participants. The study started on 2017-06-08. Estimated completion is 2018-05-04.
What interventions are being tested in trial NCT03126162?
The interventions under investigation include: InstilIing normal saline into bladder (PROCEDURE), Removal of foley catheter (PROCEDURE).
Who is sponsoring clinical trial NCT03126162?
This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.
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