Safety and Efficacy of the Alpha AMS Subretinal Implant (OX-RI)

University of Oxford

Status

Completed

Conditions

Retinitis Pigmentosa

Treatments

Device: Implant 'on' vs implant 'off'

Study type

Interventional

Funder types

Other

Identifiers

NCT02720640

E/2015/0119

Details and patient eligibility

About

The aim of this single-centre study is to assess the safety and efficacy of the Retina Implant Alpha AMS (Retina Implant AG, Reutlingen, Germany) in participants with severe visual impairment secondary to outer retinal degeneration caused by retinitis pigmentosa (RP). The study is sponsored by the University of Oxford and funded by the National Institute for Health Research (UK).

Full description

The specific research questions are, i) can the implant partially restore vision to an eye with no light perception and ii) what are the safety implications for the ocular and periorbital tissues of the implanted eye? In advanced RP the light detecting photoreceptor cells of the retina degenerate slowly over time, and may eventually lead to blindness. The subretinal implant replaces the degenerate photoreceptor layer and stimulates the residual overlying healthy retinal layers in response to a light stimulus. These signals are then carried on to the brain along the normal visual pathway. Investigators are seeking to recruit six participants who fulfill the eligibility criteria, which include advanced RP with no useful light perception vision in the eye to receive the implant. Participants must be aged between 18 and 70 years old, be highly motivated, and be well enough for a general anaesthetic. The eye must have also had cataract surgery. The project will be conducted at the Oxford Eye Hospital. Those participants selected to receive the implant will be followed for 12 months from the date of surgery. Between week 1 and month 12 there will be at least 7 outpatient clinic visits for a range of visual tests and eye assessments. After 12 months the trial will officially end, however investigators will continue to review all research participants in clinic as would be standard care for a patient with RP. The implant may be removed at any stage e.g. when it ceases to function or at the participant's request.

Enrollment

6 patients

Sex

All

Ages

18 to 70 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Participant is willing and able to give informed consent for participation in the trial.
Male or Female, aged 18 to 70 years old.
Hereditary retinal degeneration of the outer retinal layers i.e. photoreceptor rods & cones.
Angiography shows retinal vessels adequately perfused, despite pathological RP condition.
Severe visual impairment (at least monocular) i.e. visual functions insufficient for localization of objects, self-sustained navigation and orientation e.g. impaired light localization or worse.
Ability to read normal print in earlier life, optically corrected (without magnifying glass).
Able to participate in the study during the full time period of one year.
Pseudophakic in the eye to receive the implant.
Stable dose of current regular medication for at least four weeks prior to trial entry.
Female participants of child bearing potential must be willing to ensure that they or their partner use effective contraception during the trial.
Participant has clinically acceptable laboratory and ECG results as confirmed at - Screening Visit and upon review by consultant anaesthetist.
In the Investigator's opinion, is able and willing to comply with all trial requirements.
Willing to allow his or her General Practitioner and consultant, if appropriate, to be notified of participation in the trial.

Exclusion criteria

Period of appropriate visual functions < 12 years / lifetime.
Optical coherence tomography (OCT) shows significant retina oedema &/or scar tissue within target region for implant.
Retina detected as too thin to expect required functionality of inner retina as shown via OCT.
Lack of inner-retinal function, as determined by Electrically Evoked Phosphenes (EEP).
Heavy clumped pigmentation at posterior pole.
Any other ophthalmologic disease with relevant effect upon visual function (e.g. glaucoma, optic neuropathies, trauma, diabetic retinopathy, retinal detachment).
Amblyopia reported earlier in life for eye to be implanted.
Systemic diseases that might imply considerable risks with regard to the surgical interventions and anesthesia (e.g. cardiovascular/ pulmonary diseases, significant metabolic diseases e.g. diabetes).
Neurological and/or psychiatric diseases (e.g. Parkinson, epilepsy, depression).
Hyperthyroidism or hypersensitivity to iodine.
Hypersensitivity to fluorescent dye (fluorescence angiography).
Women who are pregnant or nursing, or women of childbearing age who are not willing to use a medically acceptable means of birth control for the duration of the study, or women unwilling to perform a pregnancy test before entering the study.
Participation in another interventional clinical trial within the past 12 weeks.
Scheduled elective surgery or other procedures requiring general anaesthesia during the trial.
Any other significant disease or disorder which, in the opinion of the Investigator, may either put the participants at risk because of participation in the trial, or may influence the result of the trial, or the participant's ability to participate in the trial.