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NCT01583166 · ClinicalTrials.gov registry record · NA
Voiding Function After Mid-Urethral Slings With and Without Local Anesthetic: Randomized Controlled Trial
A NA study, sponsored by University of Massachusetts, Worcester.
- Completed
- Registry status
- NA
- Development phase
- 90
- Enrollment target
NCT01583166 is a NA study that has completed, run by University of Massachusetts, Worcester. The registered enrollment target is 90 participants.
The verdict
NCT01583166, a NA study, has completed, sponsored by University of Massachusetts, Worcester.
- COMPLETED
- Registry status
- NA
- Development phase
- 90 participants
- Enrollment target
Study Summary
The purpose of this study is to determine if there is a difference in post-operative voiding function between subjects receiving local anesthetic and those receiving placebo at the time of mid-urethral sling placement. The secondary objective is to evaluate pain after the procedure in the two groups.
Interventions
- DRUG Bupivacaine
- DRUG Epinephrine
- DRUG Saline
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 90 participants |
| Start Date | 2012-03 |
| Est. Completion | 2016-05 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01583166
The ClinicalTrials.gov registry entry for NCT01583166 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 90 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Massachusetts, Worcester, which has 240 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 3 interventions - of which Bupivacaine is the first listed.
NCT01583166 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01583166 about?
NCT01583166 is a clinical study titled "Voiding Function After Mid-Urethral Slings With and Without Local Anesthetic: Randomized Controlled Trial". The purpose of this study is to determine if there is a difference in post-operative voiding function between subjects receiving local anesthetic and those receiving placebo at the time of mid-urethral sling placement. The secondary objective is to evaluate pain after the procedure in the two groups...
What is the current status of trial NCT01583166?
This trial is currently completed. It is a NA study. The enrollment target is 90 participants. The study started on 2012-03. Estimated completion is 2016-05.
What interventions are being tested in trial NCT01583166?
The interventions under investigation include: Bupivacaine (DRUG), Epinephrine (DRUG), Saline (DRUG).
Who is sponsoring clinical trial NCT01583166?
This trial is sponsored by University of Massachusetts, Worcester, which has 240 total clinical trials registered on ClinicalTrials.gov.
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