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

Capsular Bag Distention Syndrome After Cataract Surgery Clinical Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01868217
• Other study ID #: NSFC-81100653
• Status: Completed
• Phase: N/A
• First received: May 27, 2013
• Last updated: May 30, 2013
• Start date: January 2013

Study information

• Verified date: May 2013
• Source: Evidence Based Cataract Study Group
• Contact: n/a
• Is FDA regulated: No
• Health authority: China: National Natural Science Foundation of China
• Study type: Observational

Clinical Trial Summary

• To Investigate the Prevalence of Capsular Bag Distention Syndrome

• To Analyze Influencing Factors of Capsular Bag Distention Syndrome

Recruitment information / eligibility

• Status: Completed
• Enrollment: 239
• Est. primary completion date: March 2013
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 45 Years to 90 Years

Eligibility

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.

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

• Capsular Bag Distention Syndrome After Cataract Surgery
• Capsule Opacification

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Evidence Based Cataract Study Group

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Dimension of the eyeball(mm)		1 month	No