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Evaluation of Cardiorespiratory Events in Subjects Undergoing an Upper and/or Lower Endoscopy Under Current Sedation Practices

NCT00559260 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 300

Last updated 2008-09-15

No results posted yet for this 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.

Conditions

  • Sedation for Non-Emergent Upper and/or Lower Endoscopy

Interventions

DEVICE

Passive monitoring with pulse-oximetry, NIBP and ECG

Sponsors & Collaborators

  • Ethicon Endo-Surgery

    lead INDUSTRY

Principal Investigators

  • Philip Miner, MD · Oklahoma Foundation for Digestive Research

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-01-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00559260 on ClinicalTrials.gov