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OpenTrials
Completed

NCT Number: NCT01745341

Rates of Apnea in Patients Undergoing Vitreoretinal Surgery

The purpose of this study is to determine if apnea (the stopping of breathing) occurs in patients undergoing undergoing monitored anesthesia care (MAC) for vitreoretinal surgery

Completed

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Key information

Age range

18 year–99 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Stanford Hospital and Clinics

Palo Alto, California, 94303, United States

About this study

Patients undergoing vitreoretinal surgery will be monitored during the procedure to determine if they stop breathing. This study is observational in nature and no interventions will be made.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients having vitreoretinal surgery under monitored anesthesia care

Exclusion criteria

  • patients having vitreoretinal surgery without monitored anesthesia care

Treatment and study plan

Primary outcomes

  1. Apnea

    Time frame: 15 minutes

    Determine if patients undergoing vitreoretinal surgery under monitored anesthesia care stop breathing during the procedure

Sponsors and collaborators

Lead sponsor

Stanford University

Other

Registry information

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Dec 10, 2012
Registry last updated
Dec 3, 2015

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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