Clinical Characteristics in Congenital Cataract Eyes

Sponsor
yin ying zhao (Other)
Overall Status
Completed
CT.gov ID
NCT03905044
Collaborator
(none)
239
92

Study Details

Study Description

Brief Summary

This study involved children with congenial cataract eyes, who underwent cataract surgeries at the Eye Hospital of Wenzhou Medical University (Hangzhou, China). All medical records were reviewed for primary diagnosis. All surgeries were performed by one experienced surgeon (Z.Y.E) and videos were collected for reviews in details. the clinical data after the surgery were also recorded for further analysis.

Condition or Disease Intervention/Treatment Phase
  • Other: eyes with congenital cataracts

Study Design

Study Type:
Observational
Actual Enrollment :
239 participants
Observational Model:
Other
Time Perspective:
Retrospective
Official Title:
Clinical Characteristics of Three Pathological Types of Posterior Capsule Abnormality in Congenital Cataract Eyes
Actual Study Start Date :
Jan 1, 2011
Actual Primary Completion Date :
Aug 31, 2018
Actual Study Completion Date :
Aug 31, 2018

Arms and Interventions

Arm Intervention/Treatment
CC

eyes with congenital cataracts

Other: eyes with congenital cataracts
observation

Outcome Measures

Primary Outcome Measures

  1. complication rate [3 months]

    the complication occurrent rate

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Day to 18 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • children with congenital cataracts who underwent cataract surgeries at the Eye Hospital of Wenzhou Medical University (Hangzhou, China)
Exclusion Criteria:
  • ocular trauma

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • yin ying zhao

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
yin ying zhao, Clinical professor, Wenzhou Medical University
ClinicalTrials.gov Identifier:
NCT03905044
Other Study ID Numbers:
  • DXX-CC
First Posted:
Apr 5, 2019
Last Update Posted:
Apr 5, 2019
Last Verified:
Apr 1, 2019
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 5, 2019