Active, not recruitingNot applicableNCT06109285
Validation of i-ROP DL to Detect More Than Mild ROP
Studying Retinopathy of prematurity
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Siloam Vision
- Principal Investigator
- John P Campbell, MD/MPHOregon Health and Science University
- Intervention
- iROP DL(device)
- Enrollment
- 16 enrolled
- Eligibility
- 20-80 years · All sexes
- Timeline
- 2024 – 2026
Study locations (1)
- Oregon Health and Sciences University, Portland, Oregon, United States
Collaborators
National Eye Institute (NEI)
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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