- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01745341
Rates of Apnea in Patients Undergoing Vitreoretinal Surgery
December 2, 2015 updated by: Theodore Leng, Stanford University
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
Study Overview
Status
Completed
Conditions
Detailed 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.
Study Type
Observational
Enrollment (Actual)
113
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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California
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Palo Alto, California, United States, 94303
- Stanford Hospital and Clinics
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 99 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
patients having vitreoretinal surgery under monitored anesthesia care
Description
Inclusion Criteria:
- patients having vitreoretinal surgery under monitored anesthesia care
Exclusion Criteria:
- patients having vitreoretinal surgery without monitored anesthesia care
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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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.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Apnea
Time Frame: 15 minutes
|
Determine if patients undergoing vitreoretinal surgery under monitored anesthesia care stop breathing during the procedure
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15 minutes
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2012
Primary Completion (Actual)
August 1, 2013
Study Completion (Actual)
August 1, 2013
Study Registration Dates
First Submitted
December 5, 2012
First Submitted That Met QC Criteria
December 7, 2012
First Posted (Estimate)
December 10, 2012
Study Record Updates
Last Update Posted (Estimate)
December 3, 2015
Last Update Submitted That Met QC Criteria
December 2, 2015
Last Verified
December 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 25284
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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