Potential Environmental Causes of Uveal Coloboma
Pilot Evaluation of Potential Environmental Causes of Uveal Coloboma
2 other identifiers
observational
76
1 country
1
Brief Summary
Background: Uveal coloboma is a congenital eye malformation. It is thought to be a genetic condition. But it might have environmental causes as well. Researchers want to study the mothers of children with coloboma. They will use parts of the National Birth Defects Prevention Study (NBDPS) Mother Questionnaire. NBDPS was a large study of birth defects. It collected data from 1997 to 2011. Researchers will use NBDPS and NIH data as well as the new survey to produce data that can serve as a basis for further study. Objective: To explore maternal factors and exposures during the first trimester of pregnancy as potential causes of uveal coloboma and to correlate exposure data to clinical data from affected children. Eligibility: Mothers of probands with coloboma who have taken part in NIH study 06-EI-0230, 04-EI-0039, or 13-EI-0049. Design: This is a hybrid study. It will use existing data from NBDPS and NIH studies. It will also use NBDPS for a new survey of mothers of children with coloboma. Participants will take the survey by phone. Their pregnancy records may be reviewed. They will be asked about: Important dates Health and medicines Tobacco, alcohol, and substance use Parents occupations Family demographics. The survey will take 1 hour or less to complete. Some data were obtained in past NIH studies. These data are largely from children. Some family data may be used as well. For example, eye exam data, gene test results, and family history of coloboma may be used. If a participant did not consent to the future use of their data, then their data will not be used. Data will be stored in a secure NIH database. ...
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Jun 2023
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 5, 2021
CompletedFirst Posted
Study publicly available on registry
April 6, 2021
CompletedStudy Start
First participant enrolled
June 20, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 17, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
March 17, 2025
CompletedOctober 2, 2025
September 30, 2025
1.7 years
April 5, 2021
October 1, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
% of participants with x exposure compared to historical data
% of participants with x exposure compared to historical data from NBDPS study.
ongoing
Study Arms (1)
Mothers
Mothers of children with coloboma.
Eligibility Criteria
Up to 180 mothers of probands with coloboma that have previously been consented to an NIH protocol studying coloboma.
You may qualify if:
- mothers of probands with coloboma that have previously been consented to an NIH protocol studying coloboma.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
National Eye Institute (NEI)
Bethesda, Maryland, 20892, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Brian P Brooks, M.D.
National Eye Institute (NEI)
Study Design
- Study Type
- observational
- Observational Model
- FAMILY BASED
- Time Perspective
- OTHER
- Sponsor Type
- NIH
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
April 5, 2021
First Posted
April 6, 2021
Study Start
June 20, 2023
Primary Completion
March 17, 2025
Study Completion
March 17, 2025
Last Updated
October 2, 2025
Record last verified: 2025-09-30