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 |
---|---|---|
|
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
- 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: