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NCT01315158 · ClinicalTrials.gov registry record · NA
Propofol vs Propofol + Benzo/Opiates in High Risk Group
A NA study, sponsored by Washington University School of Medicine.
- Terminated
- Registry status
- NA
- Development phase
- 36
- Enrollment target
NCT01315158 is a NA study that was terminated before completion, run by Washington University School of Medicine. The registered enrollment target is 36 participants.
The verdict
NCT01315158, a NA study, was terminated before completion, sponsored by Washington University School of Medicine.
- TERMINATED
- Registry status
- NA
- Development phase
- 36 participants
- Enrollment target
Study Summary
This will be a randomized controlled trial that compares the rates of sedation related complications in high risk patients (ASA greater or equal to 3, BMI greater or equal to 30, those at risk for OSA) undergoing advanced endoscopy procedures with propofol alone compared to propofol in combination with benzodiazepines and opioids.
Interventions
- DRUG Propofol Alone
- DRUG Propofol+Benzo/Opioids
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 36 participants |
| Start Date | 2011-01 |
| Est. Completion | 2014-07 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01315158
The ClinicalTrials.gov registry entry for NCT01315158 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 36 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Washington University School of Medicine, which has 1,502 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Propofol Alone is the first listed.
NCT01315158 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT01315158 about?
NCT01315158 is a clinical study titled "Propofol vs Propofol + Benzo/Opiates in High Risk Group". This will be a randomized controlled trial that compares the rates of sedation related complications in high risk patients (ASA greater or equal to 3, BMI greater or equal to 30, those at risk for OSA) undergoing advanced endoscopy procedures with propofol alone compared to propofol in combination w...
What is the current status of trial NCT01315158?
This trial is currently terminated. It is a NA study. The enrollment target is 36 participants. The study started on 2011-01. Estimated completion is 2014-07.
What interventions are being tested in trial NCT01315158?
The interventions under investigation include: Propofol Alone (DRUG), Propofol+Benzo/Opioids (DRUG).
Who is sponsoring clinical trial NCT01315158?
This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.
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