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Macular Degeneration clinical trials

View clinical trials related to Macular Degeneration.

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NCT ID: NCT03815825 Active, not recruiting - Clinical trials for Macular Degeneration

GOLDEN STUDY: A Study to Assess Safety and Efficacy of Multiple Doses of IONIS-FB-LRx in Participants With Geographic Atrophy Secondary to Age-Related Macular Degeneration (AMD)

Start date: March 4, 2019
Phase: Phase 2
Study type: Interventional

Evaluate the effect of IONIS-FB-LRx on the rate of change of the area of geographic atrophy (GA) secondary to age-related macular degeneration (AMD) measured by fundus autofluorescence (FAF).

NCT ID: NCT03814291 Active, not recruiting - Clinical trials for Neovascular Age-related Macular Degeneration

A Dose Escalation Study of IBI302 in Patients With Wet Age-related Macular Degeneration

Start date: April 16, 2019
Phase: Phase 1
Study type: Interventional

This study is designed for single-center, open-label, dose escalation phase I trial to evaluate the safety and tolerability of a single intravitreal injection of IBI302 in patients with wet AMD.

NCT ID: NCT03803631 Active, not recruiting - AMD Clinical Trials

CNV in AMD Analyzed by OCT Angiography Under IntravitreaL Eylea (COCTAEyl)

COCTAEyl
Start date: April 4, 2018
Phase:
Study type: Observational

The main objective of this study is to analyze a new noninvasive imaging examination, OCT angiography, in the evaluation of neovascular remodeling and early signs of recurrence of wet AMD undergoing treatment on OCTA and to correlate OCTA findings with SD-OCT findings.

NCT ID: NCT03725566 Active, not recruiting - Clinical trials for Macular Degeneration

JY028 Single Vitreous Injection in a Phase 1 Clinical Trial in nAMD Patients

Start date: May 22, 2018
Phase: N/A
Study type: Interventional

Phase I clinical trial on safety, tolerance, pharmacokinetics (PK) and pharmacodynamics of recombinant human anti-VEGF monoclonal antibody injection in patients with neovascular (wet) age-related macular degeneration

NCT ID: NCT03688243 Active, not recruiting - Clinical trials for Dry Macular Degeneration

Non Exudative AMD Imaged With SS-OCT

BIRC-01
Start date: January 18, 2018
Phase:
Study type: Observational

The investigators wish to better understand the role of the choriocapillaris (CC) in the formation and progression of non-exudative in age related macular degeneration (armd) by imaging the retinal pigment epithelium (rpe) and the choroidal microvasculature and by studying their inter-dependence to determine if the loss of the CC could prove useful as an anatomic clinical trial endpoint in future drug trials.

NCT ID: NCT03630315 Active, not recruiting - Clinical trials for Neovascular Age-related Macular Degeneration

CLN-0046: Treatment of AMD Subjects With OTX-TKI

Start date: February 18, 2019
Phase: Phase 1
Study type: Interventional

To evaluate the safety, tolerability and efficacy of OTX-TKI for intravitreal use, in subjects who have neovascular age-related macular degeneration (AMD).

NCT ID: NCT03528122 Active, not recruiting - Retinal Detachment Clinical Trials

Amniotic Membrane for Recurrent Macular Hole

Start date: February 1, 2018
Phase: N/A
Study type: Interventional

Macular hole surgery were tried by different surgeons using many techniques with different successes but still there were many recurrences. In this study the investigators try to close these distinct types including recurrent holes using pre-prepared amniotic membrane.

NCT ID: NCT03478878 Active, not recruiting - Clinical trials for Age-Related Macular Degeneration

Vitamin A Palmitate Supplementation in Patients With Reticular Pseudodrusen (RPD) and Delayed Dark Adaptation

Start date: May 14, 2018
Phase: Early Phase 1
Study type: Interventional

Background: Age-related macular degeneration (AMD) is an eye disease. It is the leading cause of vision loss in people over 55 in the U.S. Changes in the eye can make it difficult for they eye to adjust to low light. This is known as dark adaptation. This is particularly significant in people with reticular pseudodrusen (RPD). Identifying and watching the early to middle stages of AMD and changes in dark adaptation might help researchers learn to stop the disease before it becomes severe. Taking vitamin A might help improve vision in people with RPD. Objectives: To see if taking 16,000 IU of vitamin A per day improves vision in people with RPD. Also to improve understanding of RPD and associated dark adaptation. Eligibility: Adults ages 50 and older with RPD and normal liver function Design: Participants will be screened with: Medical and eye disease history Eye exam: The pupil will be dilated with eye drops. Pictures will be taken of the retina and the inside of the eye. Including the screening visit, participants will have at least 5 visits. They will be about once a month over 6 months and last 4-6 hours. Visits include: Questions about eye problems in certain light Eye exam Blood and urine tests Dark adaptation protocol: Participants will sit at a machine in a dark room. They will look into the machine and push a button when they see a light. This lasts 20-40 minutes. Participants will take a vitamin A supplement by mouth once a day for 2 months. They will record when they take the pills in a diary.

NCT ID: NCT03478865 Active, not recruiting - AMD Clinical Trials

Vitamin A Palmitate Supplementation in People With Age-Related Macular Degeneration (and Without Reticular Pseudodrusen) and Delayed Dark Adaptation

Start date: April 20, 2018
Phase: Early Phase 1
Study type: Interventional

Background: Age-related macular degeneration (AMD) is an eye disease. It is the leading cause of vision loss in people over 55 in the U.S. Changes in the eye can make it difficult for the eye to adjust to low light. This is known as dark adaptation. Identifying and watching the early to middle stages of AMD and changes in dark adaptation might help researchers develop new treatments to stop the disease before it becomes severe. Taking vitamin A might help improve vision in people with AMD. Objectives: To see if taking 16,000 IU of vitamin A per day improves vision in people with AMD. Also to improve understanding of AMD and associated dark adaptation. Eligibility: Adults ages 50 and older with AMD and normal liver function Design: Participants will be screened with: Medical and eye disease history Eye exam: The pupil will be dilated with eye drops. Pictures will be taken of the retina and the inside of the eye. Including the screening visit, participants will have at least 5 visits. They will be about once a month over 6 months. Visits include: Questions about eye problems in certain light Eye exam Blood and urine tests Dark adaptation protocol: Participants will sit at a machine in a dark room. They will look into the machine and push a button when they see a light. This lasts 20-30 minutes. Participants will take a vitamin A supplement by mouth once a day for 2 months. They will record when they take the pills in a diary.

NCT ID: NCT03392324 Active, not recruiting - Clinical trials for Dry Age-related Macular Degeneration

PRIMA US-Feasibility Study in Atrophic Dry AMD

PRIMA-FS-US
Start date: April 26, 2018
Phase: N/A
Study type: Interventional

In this early feasibility trial the safety and performance of the new retinal prothesis PRIMA is tested in five subjects suffering from atrophic dry age related macular degeneration.