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NCT01745341 Clinical Trial

Rates of Apnea in Patients Undergoing Vitreoretinal Surgery

Apnea Clinical Trial

Official title:
Rates of Apnea in Patients Undergoing Vitreoretinal Surgery

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01745341
Other study ID # 25284
Secondary ID
Status Completed
Phase N/A
First received December 5, 2012
Last updated December 2, 2015
Start date August 2012
Est. completion date August 2013

Study information
Verified date December 2015
Source Stanford University
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Observational

Clinical Trial Summary

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

Description:

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.

Recruitment information / eligibility
Status Completed
Enrollment 113
Est. completion date August 2013
Est. primary completion date August 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria:

- patients having vitreoretinal surgery under monitored anesthesia care

Exclusion Criteria:

- patients having vitreoretinal surgery without monitored anesthesia care

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Locations
Country Name City State
United States Stanford Hospital and Clinics Palo Alto California

Sponsors (1)
Lead Sponsor Collaborator
Stanford University

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Apnea Determine if patients undergoing vitreoretinal surgery under monitored anesthesia care stop breathing during the procedure 15 minutes No
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