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Retinitis Pigmentosa clinical trials

View clinical trials related to Retinitis Pigmentosa.

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NCT ID: NCT01531348 Completed - Clinical trials for Retinitis Pigmentosa

Intravitreal Injection of MSCs in Retinitis Pigmentosa

Start date: April 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the feasibility and safety of adult human bone marrow-derived mesenchymal stem cells by intravitreal injection in patients with retinitis pigmentosa.

NCT ID: NCT01530659 Completed - Clinical trials for Retinitis Pigmentosa

Retinal Imaging in CNTF -Releasing Encapsulated Cell Implant Treated Patients for Early-stage Retinitis Pigmentosa

Start date: January 2012
Phase: Phase 2
Study type: Interventional

This clinical trial is a single-site, 30 patient study for participants who have early stage retinitis pigmentosa, or Usher syndrome (type 2 or 3). Funding Source - FDA OOPD and Foundation Fighting Blindness.

NCT ID: NCT01521793 Completed - Clinical trials for RP (Retinitis Pigmentosa)

Repeated Treatments of QLT091001 in Subjects With Leber Congenital Amaurosis or Retinitis Pigmentosa (Extension of Study RET IRD 01)

Start date: January 2012
Phase: Phase 1
Study type: Interventional

The purpose of this study is: - To evaluate the safety of up to 3 additional courses of oral QLT091001 administered once daily for 7 days in subjects treated previously with a single 7-day course of QLT091001 in Study RET IRD 01 - To evaluate whether up to 3 additional courses of oral QLT091001 administered once daily for 7 days can maintain or improve visual function.

NCT ID: NCT01505062 Terminated - Clinical trials for Retinitis Pigmentosa

Study of SAR421869 in Participants With Retinitis Pigmentosa Associated With Usher Syndrome Type 1B

Start date: March 26, 2012
Phase: Phase 1/Phase 2
Study type: Interventional

To evaluate the safety and tolerability of ascending doses of subretinal injections of SAR421869 in participants with Usher syndrome type 1B. To evaluate for possible biological activity of SAR421869.

NCT ID: NCT01497379 Completed - Clinical trials for Retinitis Pigmentosa

Safety & Efficacy of Subretinal Implants for Partial Restoration of Vision in Blind Patients

Start date: October 2011
Phase: N/A
Study type: Interventional

Patients who are legally blind, caused by retinal degeneration of photoreceptor rods & cones (e.g. Retinitis pigmentosa), receive a subretinal implant to restore vision partially.

NCT ID: NCT01490827 Terminated - Clinical trials for Retinitis Pigmentosa

Argus® II Retinal Prosthesis System Post-Market Surveillance Study

Start date: November 2011
Phase:
Study type: Observational

This post-market surveillance study is conducted in the European Economic Area where Argus II has been CE certified for use in outer retinal degeneration patients.

NCT ID: NCT01482195 Completed - Clinical trials for Retinitis Pigmentosa

Trial of Subretinal Injection of (rAAV2-VMD2-hMERTK)

Start date: August 2011
Phase: Phase 1
Study type: Interventional

This study was to assess the safety of gene transfer via subretinal administration of rAAV2-VMD2-hMERTK in subjects with MERTK-associated retinitis pigmentosa (RP).

NCT ID: NCT01432847 Recruiting - Clinical trials for Retinitis Pigmentosa

Cell Collection to Study Eye Diseases

Start date: September 7, 2011
Phase:
Study type: Observational

Background: - Best Vitelliform Dystrophy (Best disease), Late-Onset Retinal Degeneration (L-ORD), and Age-Related Macular Degeneration (AMD) all affect the retina, the light sensing area at the back of the eye. Doctors cannot safely obtain retinal cells to study these diseases. However, cells collected from hair follicles, skin, and blood can be used for research. Researchers want to collect cells from people with Best disease, L-ORD, and AMD, and compare their cells with those of healthy volunteers. Objectives: - To collect hair, skin, and blood samples to study three eye diseases that affect the retina: Best disease, L-ORD, and AMD. Eligibility: - Individuals affected with ocular condition is one year of age or older. - Individuals affected with Best disease, L-ORD, or AMD is 18 years of age or older. - Unaffected individuals are seven years of age or older. Design: - The study requires one visit to the National Eye Institute. - Participants will be screened with a medical and eye disease history. They will also have an eye exam. - Participants will provide a hair sample, a blood sample, and a skin biopsy. The hair will be collected from the back of the head, and the skin will be collected from the inside of the upper arm.

NCT ID: NCT01415453 Terminated - Clinical trials for Retinitis Pigmentosa

Evoked Retinal Response

Start date: July 2011
Phase: N/A
Study type: Interventional

Retinitis pigmentosa (RP) is the name given to a group of inherited eye diseases that affect the retina (the light-sensitive part of the eye). RP causes the breakdown of photoreceptor cells (cells in the retina that detect light). Photoreceptor cells capture and process light helping us to see. As these cells breakdown and die, people experience progressive vision loss. There is no known cure for retinitis pigmentosa. The investigators have observed that short pulses of focused ultrasound can cause perception of light when directed to spots on the retinal surface. The investigators propose to conduct a study to determine if pulsed ultrasound will stimulate the perception of light in the absence of functional photoreceptors in people with RP

NCT ID: NCT01399515 Completed - Clinical trials for Retinitis Pigmentosa

Efficacy and Safety of Oral Valproic Acid for Retinitis Pigmentosa

VPA_RP
Start date: March 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the efficacy and safety of oral valproic acid to slow the progression of visual function and/or to improve the visual function in patients with retinitis pigmentosa (RP). Enrolled subjects in valproic acid group will be treated with oral valproic acid 500mg daily for 48 weeks. Visual function and safety will be assess before and after treatment (48 weeks) between valproic acid and control groups.