- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07541651
Study on Eye-Brain Cross-Organ Mapping and Systemic Disease Association Based on Multimodal Big Data
April 14, 2026 updated by: Beijing Friendship Hospital
This project integrates multimodal eye data (CFP, OCT, OCTA) from 50,000 cases, brain MR data from 150,000 cases, and ICD diagnoses, medical orders, and test results from an eye-brain paired cohort of 8,000 cases to construct an eye-brain cross-modal mapping model and an eye-brain-systemic disease association model.
It aims to clarify the quantitative associations between multimodal ocular features and brain structural and vascular characteristics as well as systemic disease ICD diagnoses, thereby uncovering the cross-organ and cross-modal linkage mechanisms between the eye and brain.
Ultimately, it seeks to achieve mapping and prediction of brain imaging features based on ocular data, enable ocular-based diagnosis and prediction of various diseases, and contribute significantly to early disease screening, risk stratification, and optimization of clinical diagnosis and treatment.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
208000
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
(1) Ophthalmic Data Cohort: Patients and health check-up participants who underwent CFP , OCT or OCTA examinations at Beijing Friendship Hospital, Capital Medical University, from January 2009 to September 2025.(2)
Cerebral Data Cohort: Patients and health check-up participants who underwent cerebral MR (Magnetic Resonance) examinations at the same hospital during the corresponding period.(3)
Oculo-Cerebral Matched Cohort: Individuals from Beijing Friendship Hospital, Capital Medical University and the UK Biobank (UKB) database who had any of the above ophthalmic imaging examinations, plus cerebral MR scans, and could be matched with complete clinical information.(4)
Clinical Correlation Cohort: Individuals from the above cohorts who had complete ICD (International Classification of Diseases) diagnoses, laboratory test results (including blood glucose, blood lipids, uric acid, etc.) and medical order records at Beijing Friendship Hospital, Capital Medical University.
Description
Inclusion Criteria:
- Eye data: Images must meet quality standards (no significant artifacts, key structures clearly visible), with complete examination records (including examination date and device model).
- Brain data: MR images must be free of motion artifacts, with complete sequences (at least including T1-weighted imaging and MRA), and reports must confirm no technical issues.
- Eye-brain paired cohort: Must contain at least one type of eye image (including CFP, OCT, or OCTA) along with brain MR data, and be linkable to a unique identifier and clinical information in the database
- Clinical data: Clinical information (such as core biochemical indicators, demographic information, and necessary questionnaire items) must have a missing rate ≤30%, with standardized and clear ICD diagnostic codes, complete laboratory test data, and medical order information (including medication or follow-up recommendations)
- Prior to initial inclusion in the study, participants must have no history of severe organic diseases (including non-curable or end-stage malignancies, severe heart failure (NYHA Class III-IV), end-stage renal disease (CKD Stage 5), decompensated cirrhosis, or significant functional impairment due to severe cerebrovascular disease sequelae, etc.).
Exclusion Criteria:
- Ocular examinations in which key features cannot be identified due to conditions such as cataracts or vitreous hemorrhage brain MR images deemed unacceptable in quality due to factors such as metal implants
- Clinical information (including core biochemical indicators, demographic details, essential questionnaire items, etc.) with a missing rate exceeding 30%
- Individuals who are pregnant or lactating, those with ocular trauma, congenital ocular malformations, or severe organic diseases.
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Ophthalmic Data Cohort
|
No interventions were involved in this study.
|
|
Cerebral Data Cohort
|
No interventions were involved in this study.
|
|
Oculo-Cerebral Matched Cohort
|
No interventions were involved in this study.
|
|
Clinical Correlation Cohort
|
No interventions were involved in this study.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Performance of Systemic Disease Prediction Models
Time Frame: From the time of model construction and consistency alignment during the study period to the end of the 12-month follow-up after study initiation.
|
Age- and sex-stratified Area Under the Receiver Operating Characteristic Curve (AUC)
|
From the time of model construction and consistency alignment during the study period to the end of the 12-month follow-up after study initiation.
|
|
Model generalisation capability.
Time Frame: From the completion of model construction and consistency calibration during the study period to the end of the 12-month follow-up after study initiation.
|
Evaluated by Cohen's kappa coefficient across external independent cohorts.
|
From the completion of model construction and consistency calibration during the study period to the end of the 12-month follow-up after study initiation.
|
|
Eye-Brain Mapping Model Performance.
Time Frame: From the completion of model construction and consistency calibration during the study period to the end of the 12-month follow-up after study initiation.
|
Measured by correlation coefficient between retinal imaging features and brain neuroimaging metrics.
|
From the completion of model construction and consistency calibration during the study period to the end of the 12-month follow-up after study initiation.
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Estimated)
April 25, 2026
Primary Completion (Estimated)
December 31, 2029
Study Completion (Estimated)
December 31, 2029
Study Registration Dates
First Submitted
January 6, 2026
First Submitted That Met QC Criteria
April 14, 2026
First Posted (Actual)
April 21, 2026
Study Record Updates
Last Update Posted (Actual)
April 21, 2026
Last Update Submitted That Met QC Criteria
April 14, 2026
Last Verified
February 1, 2026
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Cerebrovascular Disorders
- Brain Diseases
- Central Nervous System Diseases
- Nervous System Diseases
- Vascular Diseases
- Cardiovascular Diseases
- Pathologic Processes
- Hemorrhage
- Eye Diseases
- Lens Diseases
- Eye Hemorrhage
- Pathological Conditions, Signs and Symptoms
- Cataract
- Cerebral Small Vessel Diseases
- Vitreous Hemorrhage
Other Study ID Numbers
- 202601
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.
Clinical Trials on Vitreous Hemorrhage
-
Al Hadi HospitalCompletedDiabetic Vitreous HemorrhageKuwait
-
Panhandle Eye Group, LLPRecruitingDiabetic Vitreous HemorrhageMexico
-
Asan Medical CenterUnknownPost Vitrectomy State | Recurrent Diabetic Vitreous HemorrhageKorea, Republic of
-
Assistance Publique - Hôpitaux de ParisCompletedRetinal Detachment | Retinal Break | Spontaneous Vitreous HemorrhageFrance
-
Kasr El Aini HospitalCompletedTractional Retinal Detachment | Diabetic Vitreous HemorrhageEgypt
-
University of Sao PauloUnknownHemorrhage | RecurrentBrazil
-
Aier School of Ophthalmology, Central South UniversityRecruitingVitreous Hemorrhage | Cataract | Rhegmatogenous Retinal Detachment | Epiretinal Membrane | Macular Disease | Vitreomacular Traction | Vitreous CloudyChina
-
University of Sao PauloUnknownVitreous Hemorrhage Secondary to PDRBrazil
-
Peregrine Eye and Laser InstituteAlcon ResearchRecruitingVitreous Hemorrhage | Retinal Detachment | Epiretinal Membrane | Vitrectomy | Macular Holes | Dislocated Intraocular Lens Into Vitreous | Retained Lens FragmentsPhilippines
-
The University of Hong KongAlcon ResearchCompletedVitreous Hemorrhage | Retinal Detachment | Epiretinal Membrane | Macula HoleHong Kong
Clinical Trials on No interventions were involved in this study.
-
Nanyang Technological UniversityMOH Office for Healthcare Transformation (MOHT), SingaporeRecruitingDepression | Stress | Anxiety | Loneliness | Positive Affect | Negative AffectSingapore
-
University of Texas Southwestern Medical CenterNational Heart, Lung, and Blood Institute (NHLBI)Active, not recruiting
-
The University of Hong KongTerminatedObstructive Sleep Apnea | Endothelial Dysfunction | Cardiac Syndrome XHong Kong
-
RenJi HospitalNot yet recruitingIdiopathic Inflammatory Myopathies
-
New York Medical CollegeRecruitingIntestinal Obstruction | Trauma Abdomen | Intestinal PerforationUnited States
-
Shenzhen Center for Disease Control and PreventionCompletedPuberty, Precocious
-
Johannes Gutenberg University MainzCompletedTBI (Traumatic Brain Injury) | Intracranial Hemorrhages | Acute Brain InjuriesGermany
-
Children's Hospital Medical Center, CincinnatiNational Institute of Diabetes and Digestive and Kidney Diseases (NIDDK); National... and other collaboratorsCompletedWolman Disease | Cholesterol Ester Storage Disease | Acid Cholesteryl Ester Hydrolase Deficiency, Type 2United States
-
Weill Medical College of Cornell UniversityCompleted
-
University of AberdeenActive, not recruitingLichen Planus, Oral | Lichen Planus of VulvaUnited Kingdom