Unknown statusInterventionalNot ApplicableUpdated Nov 17, 2017
A Retrospective Study to Investigate Prevalence of Capsular Bag Distention Syndrome and Its Influencing Factors | NCT01868217 | Trialant
CompletedObservationalUpdated Jun 4, 2013
A Retrospective Study to Investigate Prevalence of Capsular Bag Distention Syndrome and Its Influencing Factors
ClinicalTrials.gov ID
NCT01868217
Lead Sponsor
Evidence Based Cataract Study GroupOTHER
Overall Status
Completed
Study Type
Observational
Enrollment
239Actual
Last Update Posted
Jun 4, 2013Estimated
Start Date
Jan 2013
Primary Completion Date
Mar 2013Actual
Brief Summary
To Investigate the Prevalence of Capsular Bag Distention Syndrome
To Analyze Influencing Factors of Capsular Bag Distention Syndrome
Capsular Bag Distention Syndrome After Cataract Surgery
No interventions
There are no interventions for this study.
Ages Eligible for Study
Adult (18-64)Older Adult (65+)
Sexes Eligible for Study
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
patients who underwent uneventful phacoemulsification and posterior-chamber IOL implantation at the Eye and ENT Hospital of Fudan University, Xuhui, Shanghai, China, between November 2011 and December 2012
Exclusion Criteria:
Patients with traumatic cataracts or zonular weakness were excluded from the study, as were eyes with intraoperative complications, such as a posterior capsule opening, radial tearing of the continuous curvilinear capsulorhexis (CCC), or inappropriate IOL implantation.