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Validation of the Utility of Rare Disease Intelligence Platform

Validation of the Utility of Rare Disease Intelligence Platform: A Multicenter Cluster Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02748044
Enrollment
53
Registered
2016-04-22
Start date
2012-01-31
Completion date
2016-04-30
Last updated
2016-04-22

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

Conditions

Artificial Intelligence, Cataract

Brief summary

The prevention and treatment of diseases via artificial intelligence represents an ultimate goal in computational medicine. The artificial intelligence for systematic clinical application has not yet been successfully validated. Currently, the main prevention strategy for rare diseases is to build specialized care centers. However, these centers are scattered, and their coverage is insufficient, resulting in inadequate health care among a large proportion of rare disease patients. Here, the investigators use deep learning to create CC-Cruiser, an intelligence agent involving three functional networks: pick-up networks for diagnostics, evaluation networks for risk stratification and strategist networks to provide assisted treatment decisions. The investigator also establish a cloud intelligence platform for multi-hospital collaboration and conduct clinical trial and website-based study to validate its versatility.

Interventions

DEVICECC-Cruiser

An artificial intelligence to make comprehensive evaluation and treatment decision of congenital cataracts

Sponsors

Ministry of Health, China
CollaboratorOTHER_GOV
Xidian University
CollaboratorOTHER
Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients who underwent ophthalmic examination of the eye and recorded their ocular information in the collaborating hospital.

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frame
The proportion of accurate, mistaken and miss detection of CC-Cruiser.Up to 4 years

Countries

China

Outcome results

None listed

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