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Preoperative and Intraoperative Factors Related to the Development of Ptosis After Retinal Surgery | Clinical Trials | Clareo Health

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COMPLETEDNCT01752478

Preoperative and Intraoperative Factors Related to the Development of Ptosis After Retinal Surgery

The purpose of this study to is to determine the incidence of post-operative ptosis in patients undergoing vitreoretinal surgery. An additional purpose is to identify pre-operative and intra-operative...

Lead sponsor: University of California, San Francisco•1 U.S. locations•View source on ClinicalTrials.gov

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Trial snapshot

StatusCOMPLETED

Phase—

Enrollment50

Start dateJan 2013

Last updatedMay 20, 2016

Condition

Development of Ptosis After Vitreo-retinal Surgery

Locations shown

University of California, San Francisco

San Francisco, California

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: May 20, 2016Data synced to Clareo: July 13, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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