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NCT01705288 · ClinicalTrials.gov registry record · Early Phase 1
Implementation of a Rapid Recovery Program in Gynecologic Oncology Surgery: A Pilot Study
A Early Phase 1 study, sponsored by Masonic Cancer Center, University of Minnesota.
- Completed
- Registry status
- Early Phase 1
- Development phase
- 103
- Enrollment target
NCT01705288 is a Early Phase 1 study that has completed, run by Masonic Cancer Center, University of Minnesota. The registered enrollment target is 103 participants.
The verdict
NCT01705288, a Early Phase 1 study, has completed, sponsored by Masonic Cancer Center, University of Minnesota.
- COMPLETED
- Registry status
- Early Phase 1
- Development phase
- 103 participants
- Enrollment target
Study Summary
Over 600,000 hysterectomies are performed annually in the United States. Despite increasing use of less invasive approaches, the majority of hysterectomies are still performed via traditional laparotomy, which can be associated with generally slower recovery and longer lengths of post-operative hospitalization. Rapid Recovery Protocols (RRP) seek to optimize post-surgical morbidity outcomes by returning a patient to normal physiology as quickly as possible following surgery.
Interventions
- PROCEDURE Laparotomy
- DRUG intravenous narcotics
- DRUG standard anesthesia
- DRUG regional anesthesia
- DRUG Non-steroidal anti-inflammatory drugs
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 103 participants |
| Start Date | 2013-01-01 |
| Est. Completion | 2016-08-24 |
| Phase | Early Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01705288
The ClinicalTrials.gov registry entry for NCT01705288 describes a study currently listed as completed, categorized as Early Phase 1. The registered enrollment target is 103 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Masonic Cancer Center, University of Minnesota, which has 249 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 5 interventions - of which Laparotomy is the first listed.
NCT01705288 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01705288 about?
NCT01705288 is a clinical study titled "Implementation of a Rapid Recovery Program in Gynecologic Oncology Surgery: A Pilot Study". Over 600,000 hysterectomies are performed annually in the United States. Despite increasing use of less invasive approaches, the majority of hysterectomies are still performed via traditional laparotomy, which can be associated with generally slower recovery and longer lengths of post-operative hosp...
What is the current status of trial NCT01705288?
This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 103 participants. The study started on 2013-01-01. Estimated completion is 2016-08-24.
What interventions are being tested in trial NCT01705288?
The interventions under investigation include: Laparotomy (PROCEDURE), intravenous narcotics (DRUG), standard anesthesia (DRUG), regional anesthesia (DRUG), Non-steroidal anti-inflammatory drugs (DRUG).
Who is sponsoring clinical trial NCT01705288?
This trial is sponsored by Masonic Cancer Center, University of Minnesota, which has 249 total clinical trials registered on ClinicalTrials.gov.
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