Mechanisms of Retinal Revascularization and Clinical Indicators of Neovascular AMD Relapse

Wet Macular Degeneration Clinical Trial

Official title:

Mechanisms of Retinal Revascularization and Clinical Indicators of Neovascular AMD Relapse

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05211804
• Other study ID #: 21-06505
• Status: Completed
• Start date: February 8, 2022
• Est. completion date: May 21, 2024

Study information

• Verified date: March 2024
• Source: Sorlandet Hospital HF
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Age-related macular degeneration (AMD) is a chronic and progressive eye disease and is one of the leading causes of vision impairment globally. AMD is referred to as either the dry or the wet type, where the wet type (also called neovascular-AMD or nAMD) is a later stage of the disease with neovascularization and retinal edema being the main attributes. This will usually cause subacute distortion or loss of central vision in patients. Since 2004, a successful treatment alternative for nAMD has been ocular injections with anti-VEGF (anti-Vascular Endothelial Growth Factor), causing the neovascularization and edema to regress and vision to improve. However, injections have to be repeated, usually requiring 8 injections or more during the first year of treatment. This can cause both a risk for serious adverse effects and is a significant financial drain on health care resources.

Patients undergoing treatment are at risk for retinal edema recurrence. The time interval tolerated between injections is individual, and the accepted treatment strategy of today is to gradually, in a stepwise manner, increase the interval between injections. For some patients this extension is well tolerated, but for many patients relapse of proliferations and retinal edema will recur. With state-of-the-art technology OCT-A (optical coherence tomography-angiography) in combination with the clinically, well established examination method of OCT (optical coherence tomography), the project group will study the phenotypic vessel and tissue changes that occur in between injections. Furthermore, the investigators will measure cytokines, chemokines and growth factors in blood samples and the tear film during different treatment stages to see if any single factor is prognostic for poorer response to treatment or relapse.

In the short term, the project group hope that the knowledge gained from this project could lead to a better understanding of the mechanisms behind nAMD neovascular relapse and to apply this to routine screening in the clinics. In the longer term, the project group hope that elucidating the physical mechanisms and molecular changes could enable new targeted therapies to be developed.

Aim 1: To characterize the phenotype of vessels in relapsing nAMD patients and compare to those without relapse using OCT-A imaging Aim 2: To investigate retinal edema and choroidal thickness in correlation with neovascular changes of relapsing nAMD Aim 3: To measure cytokines, chemokines and growth factors in the tear film before and during treatment with anti-VEGF for nAMD

With our main hypothesis being: Relapse of nAMD in patients occurs principally through reconfiguration and vasodilatation of persistent non-regressed vessels following anti-VEGF treatment, while fully regressed vessels remain dormant

Recruitment information / eligibility

• Status: Completed
• Enrollment: 31
• Est. completion date: May 21, 2024
• Est. primary completion date: May 21, 2024
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients have to be 18 years or older

• Newly diagnosed nAMD (group 1) or nAMD treatment for at least 1 year (group 2), both with typical neovascular findings on OCT-A

• Patients with acceptable travel distance to the hospital

• Patients accepting to be part of the study

Exclusion Criteria:

• Other non-AMD macular disorders

• A spherical equivalent of -6 diopters or less

• Opacities of the visual axis; Changes of the cornea, anterior chamber, lens or vitreous cavity causing image acquisition artefacts

• Patients not able to attend extra controls due to age, illnesses or other factors

• Contraindications of intraocular injection therapy; Active ocular or periocular infection, active and serious intraocular inflammation, hypersensitivity to the drug or recent stroke / heart attack

Related Conditions & MeSH terms

• Macular Degeneration
• Wet Macular Degeneration

Intervention

Drug:
• Ophthalmic Drugs
Patients will receive the same treatment as if not a part of the project

Locations

Country	Name	City	State
Norway	Sorlandet Hospital HF	Arendal	Agder

Sponsors (1)

Lead Sponsor	Collaborator
Sorlandet Hospital HF

Country where clinical trial is conducted

Norway, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Neovascular changes during nAMD relapse assessed by the use of Optical Coherence Tomography Angiography	Images gathered from OCTA imaging will be collected and vessel phenotype will be compared between different treatment stages to identify how vessels develop over time. The attributes that will be measured are feeder vessel thickness and to assess if new vessels develop "de novo" or by using old vessel pathways. The investigators intend to describe these findings and there are no planned metric measurements. This outcome is considered a descriptive, qualitative outcome.	12 months after inclusion of patients
Secondary	Choroidal thickness in nAMD patients undergoing treatment with anti-VEGF will be measured by the use of a caliper tool (metric scale) in the Optical Coherence Tomography software	Choroidal thickness will be measured by the use of a caliper tool in the OCTA software and the thickness measured will be compared between different treatment stages of nAMD.	12 months after inclusion of patients
Secondary	Tear film of nAMD patients at different treatment stages to be collected by Schirmers test and further biochemically analysed	Levels of cytokines, chemokines and growth factors will be compared between the different treatment stages of nAMD. This will also be compared to the different levels detected i blood samples done at the same time points. Only for the treatment-naïve group.	12 months after inclusion of patients
Secondary	Blood samples of nAMD patients at different treatment stages will be collected in microtubes and further biochemically analysed	Levels of cytokines, chemokines and growth factors will be compared between the different treatment stages of nAMD. This will also be compared to the different levels detected i tear samples done at the same time points. Only for the treatment-naïve group.	12 months after inclusion of patients