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NCT01033786 · ClinicalTrials.gov registry record
Robotic Urogynecological Surgery: Hospital Stay and Perioperative Complications
A clinical trial of Urogynecology, sponsored by University of Rochester.
- Completed
- Registry status
- 21
- Enrollment target
- 1
- Study location
NCT01033786 is a study of Urogynecology that has completed, run by University of Rochester. The registered enrollment target is 21 participants. The trial reports 1 study location across 1 state.
The verdict
NCT01033786, a study of Urogynecology, has completed, sponsored by University of Rochester.
- COMPLETED
- Registry status
- 21 participants
- Enrollment target
- 1
- Study location
Study Summary
The purpose of this study is to assess length of hospital stay and perioperative complications of patients undergoing daVinci Robot-assisted sacrocolpopexy, during a one-year time period, who did not complete a questionnaire on post-operative recovery.
Conditions Studied
Study Locations (1)
New York
- University of Rochester - Rochester
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 21 participants |
| Start Date | 2009-10 |
| Est. Completion | 2009-10 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01033786
The ClinicalTrials.gov registry entry for NCT01033786 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 21 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Rochester, which has 636 total studies on file at ClinicalTrials.gov.
The record links to 1 condition, with Urogynecology appearing as the primary indexed condition, and to 0 interventions.
NCT01033786 reports 1 study location spanning 1 distinct geographic area - top geographies include New York.
Frequently Asked Questions
What is clinical trial NCT01033786 about?
NCT01033786 is a clinical study titled "Robotic Urogynecological Surgery: Hospital Stay and Perioperative Complications". The purpose of this study is to assess length of hospital stay and perioperative complications of patients undergoing daVinci Robot-assisted sacrocolpopexy, during a one-year time period, who did not complete a questionnaire on post-operative recovery.
What is the current status of trial NCT01033786?
This trial is currently completed. The enrollment target is 21 participants. The study started on 2009-10. Estimated completion is 2009-10.
What conditions does trial NCT01033786 study?
This clinical trial studies the following conditions: Urogynecology.
Who is sponsoring clinical trial NCT01033786?
This trial is sponsored by University of Rochester, which has 636 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT01033786 being conducted?
This trial has 1 study location across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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