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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: Completed study, sponsored by Ethicon Endo-Surgery.

NCT00559260 is a clinical trial that has completed, run by Ethicon Endo-Surgery. The registered enrollment target is 300 participants. According to ClinicalTrials.gov, the official US trial registry.

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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

FieldValue
Enrollment Target 300 participants
Start Date 2003-01
Ethicon Endo-Surgery

39 total trials

What the finished NCT00559260 record still lists

NCT00559260 is an observational study that tracks outcomes without assigning an intervention. The registered 300 participants enrollment target is mid-sized for trials with a published cap.

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 does not publish any study locations in the registry export this page uses.

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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Source: ClinicalTrials.gov NCT00559260, the US trial registry maintained by the National Library of Medicine. NCT00559260 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.