Clinical Trials Logo

Retinitis clinical trials

View clinical trials related to Retinitis.

Filter by:

NCT ID: NCT03998384 Not yet recruiting - Clinical trials for Retinitis Pigmentosa

A New Treatment of Retinitis Pigmentosa

Start date: January 1, 2020
Phase: N/A
Study type: Interventional

This study is designed to assess and to evaluate the therapeutic effect of retrobulbar injection of autoserum in the treatment of retinitis pigmentosa.

NCT ID: NCT03990727 Recruiting - Clinical trials for Retinitis Pigmentosa

Phenotype Correlates Genotype of Inherited Retina Dystrophies, Retinitis Pigmentosa, Con>Rod Dystrophies.

Start date: August 2009
Phase:
Study type: Observational [Patient Registry]

Patients with retina dystrophies (retinitis pigmentosa, cone>rods dystrophies, Usher and syndromic) will be correlated with genotype and validate inheritance mode by segregation analysis.

NCT ID: NCT03989622 Not yet recruiting - Clinical trials for Retinitis Pigmentosa Syndrome

Evaluation of the Visual Field on the Ground

ECVS
Start date: October 2019
Phase: N/A
Study type: Interventional

Retinopathy pigmentosa (which affects about 40,000 patients in France) leads to destruction of the peripheral retina. This condition, often familial, frequently affects young patients. Visual acuity is excellent for a long time, the disease affecting the central macular region only belatedly. On the other hand, the visual field is very quickly narrowed to a central or paracentral zone. For the patient, knowing the limits of his visual field and learning to adapt is necessary especially when traveling. The management of these patients is twofold: - an orthoptist carries out an overall evaluation of the visual field using the Goldmann device (30 cm projection of the areas seen and not seen by the patient's eye), then performs rehabilitation over several weeks - an instructor of locomotion (open specialization: occupational therapist, case of this project,...) carries out an evaluation in situation, followed by a personalized reeducation over several weeks. The first sessions consist in establishing a climate of confidence, presenting the objectives of the management of locomotion and begin to understand the movements inside and outside accompanied. The following of the rehabilitation is an apprenticeship of the optimal use of the residual field of vision and the proposed technical aids (white cane), in the whole of the displacements, inside and outside. The residual field of vision is evaluated by a device at the first appointment at the specialized center. This examination, necessary for the professional, is not informative for the patient. It is sometimes supplemented by the evaluation of the visual field of view (ECVS). The ECVS, done jointly by the orthoptist and the locomotion instructor, consists in evaluating the functional visual field on a horizontal plane at 1m (meter) and 5m, and vertical at 5m. The field of vision of the patient, immobile, is materialized by targets deposited at each limit of the zones seen that it indicates. The investigators believe that the passing of a visual field on the ground, thanks to the projection of the zones of vision, allows the patient to improve his knowledge on his visual possibilities (and gaps) and thus to make his reeducation more efficient.

NCT ID: NCT03975543 Active, not recruiting - Clinical trials for Retinitis Pigmentosa (RP)

Retrospective Natural History Study of Retinitis Pigmentosa

PHENOROD1
Start date: October 1, 2018
Phase:
Study type: Observational

This is natural history study of rods and cones degenerations in patients with Retinitis Pigmentosa (RP) caused by pathogenic mutations in RHO, PDE6A or PDE6B gene mutations.

NCT ID: NCT03963154 Active, not recruiting - Clinical trials for Retinitis Pigmentosa

Interventional Study of Implantation of hESC-derived RPE in Patients With RP Due to Monogenic Mutation

Start date: August 19, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

Phase I/II open-label, safety, tolerability and preliminary efficacy study of implantation into one eye of hESC-derived RPE (Human Embryonic Stem Cell Derived Retinal Pigment Epithelium (RPE)) in patients with retinitis pigmentosa due to monogenic mutation. Study non randomized single group assignment consisting in 2 sequential cohorts of patients: - First cohort of 2 patients with very advanced loss of visual acuity (legally blind) - Second cohort of 10 patients with less advanced loss of visual acuity:

NCT ID: NCT03944239 Recruiting - Clinical trials for Retinitis Pigmentosa

Safety and Efficacy of Subretinal Transplantation of Clinical Human Embryonic Stem Cell Derived Retinal Pigment Epitheliums in Treatment of Retinitis Pigmentosa

Start date: May 2020
Phase: Phase 1
Study type: Interventional

This project intends to transplant a clinical level human embryonic stem cells derived retinal pigment epithelium into subretinal space to treat eetinitis pigmentosa(RP) diseases. Through the statistical analysis EDTRS, BCVA, OCT, ERG, Fluorescein angiography, Ophthalmic AB ultrasound changes between before and after the treatment to assess the efficacy and safety 0f RPE transplants to treat RP disease.

NCT ID: NCT03901391 Completed - Clinical trials for Retinitis Pigmentosa

Prospective Open Clinical and Genetic Study of Patients With Retinitis Pigmentosa

RU-RP
Start date: March 26, 2019
Phase:
Study type: Observational

This study is aimed to characterize Russian population of Retinitis Pigmentosa

NCT ID: NCT03845218 Recruiting - Clinical trials for Retinitis Pigmentosa

Retinitis Pigmentosa Clinical Measures and Repeatability Testing of Potential Outcome Measures

Start date: September 27, 2019
Phase:
Study type: Observational

Background: Retinitis pigmentosa (RP) is a group of blinding eye diseases. It is caused mostly by mutations in photoreceptor-expressed genes. RP affects about 2 million people globally. There is no cure, butut treatment and diagnosis can be guided by certain tests. Researchers want to see how well these tests capture stages of RP. Objectives: To find out how well certain tests track changes in retinitis pigmentosa. Eligibility: People ages 12 and older with RP Design: Participants will be screened in another protocol. Participants will have 2 visits about 6 weeks apart. Both will include all the tests below. Each visit will last 5 6 hours, or a visit can be split into 2 days. Participants will give their medical and eye history. Participants will have an eye exam. Their pupils will be dilated with eye drops. Participants will give blood samples. Pictures of participants retinas will be taken. Their retinas will be measured. Participants will take several eye tests. They will: Sit in a dark room and press a button when they see lights. View a bright background then press a button when they see lights. Look into a bowl and press a button when they see lights. Sit in the dark with their eyes patched. Then they will take eye-numbing drops and wear contacts as lights flash. A small electrode taped to their forehead will record signals from their retinas. Minors will give written consent to stay in the study when they turn 18. After the study ends, they may also be asked to give consent for researchers to continue to use their study information. Sponsoring Institute: National Eye Institute

NCT ID: NCT03780257 Completed - Clinical trials for Retinitis Pigmentosa

Study to Evaluate Safety and Tolerability of QR-421a in Subjects With RP Due to Mutations in Exon 13 of the USH2A Gene

Stellar
Start date: March 6, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and tolerability of QR-421a administered via intravitreal injection (IVT) in subjects with Retinitis Pigmentosa (RP) due to mutations in exon 13 of the USH2A gene.

NCT ID: NCT03772938 Enrolling by invitation - Clinical trials for Retinitis Pigmentosa

Stem Cells Therapy in Degenerative Diseases of the Retina

Start date: December 13, 2018
Phase: Phase 1
Study type: Interventional

The purpose of this study is to test the safety and effectiveness of an autologous bone marrow-derived stem/progenitor cells administered intravitreously in the subjects with degenerative diseases of the retina.