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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.

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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

Sponsor

Ethicon Endo-Surgery

39 total trials

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.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.