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NCT00559260 · ClinicalTrials.gov registry record
Evaluation of Cardiorespiratory Events in Subjects Undergoing an Upper and/or Lower Endoscopy Under Current Sedation Practices
A clinical trial, sponsored by Ethicon Endo-Surgery.
- Completed
- Registry status
- 300
- Enrollment target
NCT00559260 is a clinical trial that has completed, run by Ethicon Endo-Surgery. The registered enrollment target is 300 participants.
The verdict
NCT00559260 has completed, sponsored by Ethicon Endo-Surgery.
- COMPLETED
- Registry status
- 300 participants
- Enrollment target
Study Summary
This is a 300 subject prospective study to assess cardiorespiratory events associated with current practice sedation (150 subjects; opioid + benzodiazepine) versus anesthesia provider sedation (150 subjects; propofol) for upper and/or lower endoscopy.
Interventions
- DEVICE Passive monitoring with pulse-oximetry, NIBP and ECG
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 300 participants |
| Start Date | 2003-01 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00559260
The ClinicalTrials.gov registry entry for NCT00559260 describes a study currently listed as completed, categorized as an unspecified phase. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Ethicon Endo-Surgery, which has 39 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 1 intervention - of which Passive monitoring with pulse-oximetry, NIBP and ECG is the first listed.
NCT00559260 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT00559260 about?
NCT00559260 is a clinical study titled "Evaluation of Cardiorespiratory Events in Subjects Undergoing an Upper and/or Lower Endoscopy Under Current Sedation Practices". This is a 300 subject prospective study to assess cardiorespiratory events associated with current practice sedation (150 subjects; opioid + benzodiazepine) versus anesthesia provider sedation (150 subjects; propofol) for upper and/or lower endoscopy.
What is the current status of trial NCT00559260?
This trial is currently completed. The enrollment target is 300 participants. The study started on 2003-01.
What interventions are being tested in trial NCT00559260?
The interventions under investigation include: Passive monitoring with pulse-oximetry, NIBP and ECG (DEVICE).
Who is sponsoring clinical trial NCT00559260?
This trial is sponsored by Ethicon Endo-Surgery, which has 39 total clinical trials registered on ClinicalTrials.gov.
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