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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01868217
Enrollment
239
Registered
2013-06-04
Start date
2013-01-31
Completion date
Unknown
Last updated
2013-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Capsular Bag Distention Syndrome After Cataract Surgery

Brief summary

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

Interventions

None listed

Sponsors

Evidence Based Cataract Study Group
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
45 Years to 90 Years
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Dimension of the eyeball(mm)1 month

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026