A Retrospective Study to Investigate Prevalence of Capsular Bag Distention Syndrome and Its Influencing Factors

* To Investigate the Prevalence of Capsular Bag Distention Syndrome * To Analyze Influencing Factors of Capsular Bag Distention Syndrome

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Key information

Conditions

Capsular Bag Distention Syndrome After Cataract Surgery

Age range

45 year–90 year

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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.

Treatment and study plan

Primary outcomes

Dimension of the eyeball(mm)

Time frame: 1 month

Sponsors and collaborators

Lead sponsor

Evidence Based Cataract Study Group

Other

Registry information

Important dates

Study start: 2013
Primary completion: 2013
First posted: Jun 4, 2013
Registry last updated: Jun 4, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.