Optimizing the Treatment Strategy for Age-related Macular Degeneration

  • STATUS
    Recruiting
  • participants needed
    250
  • sponsor
    St. Olavs Hospital
Updated on 19 February 2024
age-related macular degeneration
treatment protocols
macular degeneration

Summary

The purpose of this study is to compare two different treatment protocols for wet macular degeneration; the new protocol called "Observe and Plan" against the current standard protocol "Treat and Extend". Studies suggest that patients achieve equally good visual acuity with fewer controls and that they are more satisfied with the new protocol.

Description

The purpose of the study is to test a new treatment protocol for wet macular degeneration, called "Observe and Plan", against today's standard protocol "Treat and Extend". Studies suggest that the individual treatment interval can be achieved earlier with "Observe-and-Plan" and that a proportion of patients do not need more than 3 injections, ie the loading dose. The other advantages seem to be that patients achieve good visual acuity with fewer controls and are more satisfied with the new protocol, which will be beneficial to both patients and health care. To our knowledge, no randomized controlled trial has tested this before.

Details
Condition Wet Macular Degeneration, age-related macular degeneration, macular degeneration, macular degeneration
Age 50years - 100years
Treatment Observe and Plan, Treat-and-Extend
Clinical Study IdentifierNCT04420923
SponsorSt. Olavs Hospital
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

diagnosed age-related macular degeneration according to criteria
new diagnose of active CNV verified with OCTA or FA / ICGA
BCVA 20/200 measured with ETDRS visual acuity chart
written informed consent

Exclusion Criteria

Eyes formerly treated with anti-VEGF, photodynamic therapy, radiation therapy, transpupillary thermotherapy or focal laser photocoagulation involving the macular area
Geographic atrophy and subretinal fibrosis affecting the patient's visual acuity
Any other ongoing eye disease that influences patient's visual acuity, such as glaucoma with central vision loss, proliferative diabetic retinopathy, diabetic macular edema or chronic uveitis
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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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