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Spontaneous Retinal Arterial Pulsations (SRAPs) as a Prognostic Determinant of Central Retinal Vein Occlusions (CRVOs) in patients treated or not with intravitreal injections of aflibercept

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-516681-10-01
Acronym
MMT_2020_33
Enrollment
60
Registered
2024-11-12
Start date
2021-03-24
Completion date
2025-03-17
Last updated
2024-11-12

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

Conditions

central retinal vein occlusions

Brief summary

Change in visual acuity (BCVA on ETDRS scale) in letters read and validated between the start of treatment and 1 year.

Detailed description

Macular edema will be determined by the ophthalmologist from the OCT examination, Measurement of macular thickness in μm is performed using OCT-integrated measurement software, CRVO complications will be collected at one year from the patient's record, The number of aflibercept injections during the first year of follow-up will be collected at one year from the patient's record, The time between the last 2 injections of aflibercept will be collected at one year from the patient's file

Interventions

Sponsors

Fondation A De Rothschild, Fondation A De Rothschild, Fondation A De Rothschild
Lead SponsorOTHER

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Change in visual acuity (BCVA on ETDRS scale) in letters read and validated between the start of treatment and 1 year.

Secondary

MeasureTime frame
Macular edema will be determined by the ophthalmologist from the OCT examination, Measurement of macular thickness in μm is performed using OCT-integrated measurement software, CRVO complications will be collected at one year from the patient's record, The number of aflibercept injections during the first year of follow-up will be collected at one year from the patient's record, The time between the last 2 injections of aflibercept will be collected at one year from the patient's file

Countries

France

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026