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Completed Not applicable Interventional Results available

Argus® II Retinal Stimulation System Feasibility Protocol

ClinicalTrials.gov ID: NCT00407602

Public ClinicalTrials.gov record NCT00407602. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 6:51 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Investigational Phase of the Study: The objective of this feasibility study is to evaluate the safety and utility of the Argus II Retinal Stimulation System in providing visual function to blind subjects with retinitis pigmentosa. Post-Approval Phase of the Study: To collect post-approval data in order to monitor the ongoing safety and reliability of the Argus II System

Study identification

NCT ID
NCT00407602
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Second Sight Medical Products
Industry
Enrollment
30 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2006 (Type not available)
Primary completion
Dec 31, 2019 (Actual)
Completion
Dec 31, 2019 (Actual)
Last update posted
Jan 20, 2022

2006 – 2019

United States locations

U.S. sites
7
U.S. states
5
U.S. cities
6
Facility City State ZIP Site status
Doheny Eye Institute Los Angeles California 90033 —
University of California San Francisco San Francisco California 94143 —
Johns Hopkins, Wilmer Eye Institute Baltimore Maryland 21205 —
Columbia University, Department of Ophthalmology, Edward S. Harkness Eye Institute New York New York 10032 —
University of Pennsylvania, Scheie Eye Institute Philadelphia Pennsylvania 19104 —
Wills Eye Hospital Philadelphia Pennsylvania 19107 —
Retina Foundation of the Southwest Dallas Texas 75231 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00407602, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 20, 2022 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00407602 live on ClinicalTrials.gov.

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