Rates of Apnea in Patients Undergoing Vitreoretinal Surgery

NCT ID: NCT01745341

Last Updated: 2015-12-03

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

113 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-08-31

Study Completion Date

2013-08-31

Brief Summary

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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

Detailed Description

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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.

Conditions

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Apnea

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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vitreoretinal surgery patients

Patients undergoing vitreoretinal surgery under monitored anesthesia care. They will be observed during surgery and no interventions will be administered.

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* patients having vitreoretinal surgery under monitored anesthesia care

Exclusion Criteria

* patients having vitreoretinal surgery without monitored anesthesia care
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Stanford University

OTHER

Sponsor Role lead

Responsible Party

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Theodore Leng

Clinical Assistant Professor of Ophthalmology

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Stanford Hospital and Clinics

Palo Alto, California, United States

Site Status

Countries

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United States

Other Identifiers

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25284

Identifier Type: -

Identifier Source: org_study_id