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Study of OCT Peripapillary Angiography in Patients With Advanced Glaucoma - Trial NCT06274593

Access comprehensive clinical trial information for NCT06274593 through Pure Global AI's free database. This phase not specified trial is sponsored by Nantes University Hospital and is currently Not yet recruiting. The study focuses on Glaucoma. Target enrollment is 50 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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Trial Details
ClinicalTrials.gov โ€ข NCT06274593
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Study of OCT Peripapillary Angiography in Patients With Advanced Glaucoma

Study Focus

Glaucoma

OCT

Observational

device

Sponsor & Location

Nantes University Hospital

Nantes, France

Timeline & Enrollment

N/A

Apr 01, 2024

Sep 01, 2027

50 participants

Primary Outcome

Compare the progression of vascular density (VD) in advanced glaucoma patients.,Compare the progression of peripapillary retinal nerve fiber (RNFL) thickness) in advanced glaucoma patients.,Compare the progression of visual field in advanced glaucoma patients.

Summary

Glaucoma is a chronic disease of the optic nerve, characterized by progressive loss of nerve
 cells in the retina, leading to progressive loss of peripheral and central vision. There are
 in fact several types of glaucoma, which is the world's second leading cause of blindness
 after cataracts, and the leading cause of irreversible blindness.
 
 To date, to our knowledge, there is no work analyzing the progression of angiographic OCT in
 patients with glaucoma.
 
 The main aim of this study is to compare the 3-year progression rate of 3 examinations in
 advanced glaucoma patients: one functional (visual field) and two anatomical (OCTa and
 OCTrnfl).

ICD-10 Classifications

Glaucoma
Glaucoma
Other glaucoma
Glaucoma, unspecified
Glaucoma in diseases classified elsewhere

Data Source

ClinicalTrials.gov

NCT06274593

Device Trial