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Prediction Model of Treatment Efficacy for Age-related Macular Degeneration Based on Multi-source Imaging Modalities

Establishment and Application of Prediction Model of Treatment Efficacy for Age-related Macular Degeneration Based on Multi-source Imaging Modalities

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06583109
Enrollment
2600
Registered
2024-09-03
Start date
2024-10-01
Completion date
2026-06-01
Last updated
2024-09-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Age-related Macular Degeneration (ARMD)

Brief summary

Age-related macular degeneration (AMD) is one of the main causes of blindness in the elderly population. Intraocular injection of anti-VEGF drugs for neovascular AMD (nAMD) is the main treatment method at present. However, patients have different responses to anti-VEGF therapy, and some patients do not respond well to short - and long-term treatment. In this study, a retrospective study was adopted to collate and analyze the clinical data and imaging data of nAMD in the past, and to extract the imaging features from the multimodal modalities before and after treatment for deep learning, and to evaluate and quantify the clinical features, and to construct two multi-source feature models for predicting the short-term and long-term prognosis of nAMD patients. By verifying the accuracy of the model to predict the curative effect, the classification efficiency of the above characteristic models was compared, and the optimal model was selected. Its clinical application value was evaluated by calibration curve and decision curve. In addition, patients with poor treatment response in the study cohort were retrospectively analyzed, and the efficacy and safety of the combination of other treatment options in the actual clinic were analyzed. The purpose of this study is to provide scientific basis for early prediction, dynamic monitoring and optimization of overall treatment strategies for nAMD.

Interventions

None listed

Sponsors

Beijing Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
50 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patients diagnosed with nAMD by ophthalmic examinations including OCT, OCTA, FFA and ICGA; * Complete clinical data and imaging data of patients were available at baseline, 3 months and 1 year after anti-VEGF treatment.

Exclusion criteria

* Medical records showed other diseases affecting visual function or fundus imaging, such as macular edema, glaucoma, ocular trauma, etc; * Medical records showed that two or more macular lesions coexist in the affected eye; * Medical records showed that patients received other treatments within 1 year of anti-VEGF therapy, such as intraocular laser therapy or ocular surgery; * Medical records showed that there were ocular media opacity, dense macular hemorrhage, or severe macular atrophy, resulting in the inability to accurately measure the required parameters; * Medical records showed the use of drugs known to cause retinal toxicity, or a history of radiation exposure.

Design outcomes

Primary

MeasureTime frameDescription
BCVABaseline, 3 months after anti-VEGF treatment, 1 year after anti-VEGF treatmentbest-corrected visual acuity using LogMAR

Secondary

MeasureTime frameDescription
CMTBaseline, 3 months after anti-VEGF treatment, 1 year after anti-VEGF treatmentcentral macular thickness measured on OCT

Contacts

Primary ContactYUE ZHANG
962693948@qq.com18811729626

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026