- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03957642
Systematic Imaging Examination in ODD
May 21, 2019 updated by: Xiang Zhu, Third Affiliated Hospital, Sun Yat-Sen University
Diagnostic Value of Systematic Imaging Examination in Embedded Optic Disc Drusen in Adolescents With Mild Visual Impairment
To evaluate the diagnostic value of systematic ophthalmologic imaging examination in the diagnosis of embedded optic disc drusen (ODD) in adolescents with mild visual impairment.
Study Overview
Status
Unknown
Conditions
Detailed Description
Patients are evaluated through optometric examination, fundus photography, visual field examination, OCT, US, and FFA.
Study Type
Observational
Enrollment (Anticipated)
20
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Xiang Zhu, Doctor
- Phone Number: 13826452564
- Email: 0628zhuxiang@163.com
Study Locations
-
-
Guangdong
-
Guangzhou, Guangdong, China, 510630
- Recruiting
- The Third Affiliated Hospital of Sun Yat-sen University
-
Contact:
- Xiang Zhu, Doctor
- Phone Number: 13826452564
- Email: 0628zhuxiang@163.com
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years to 28 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Adolescents with mild visual impairment accompanied by disc flushing, crowded optic disc, and a blurred disc halo.
Description
Inclusion Criteria:
- Male or female.
- Age 14-28.
- The results of visual acuity examination suggest mild visual impairment.
- The results of ophthalmologic examination showed that the blurred degree of the local boundary of the optic disc was different and the optic disc was congested.
Exclusion Criteria:
- patients with amblyopia.
- patients with neurological disease.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
detection rate of embedded ODD
Time Frame: 1 week
|
detection rate of embedded ODD
|
1 week
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Xiuhua Jia, Dorctor, Third Affiliated Hospital, Sun Yat-Sen University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 21, 2019
Primary Completion (Anticipated)
January 1, 2020
Study Completion (Anticipated)
January 1, 2020
Study Registration Dates
First Submitted
May 19, 2019
First Submitted That Met QC Criteria
May 19, 2019
First Posted (Actual)
May 21, 2019
Study Record Updates
Last Update Posted (Actual)
May 23, 2019
Last Update Submitted That Met QC Criteria
May 21, 2019
Last Verified
May 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- Systematic Imaging Examination
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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