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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01542866
Other study ID # CRFB002A2407
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 11, 2011
Est. completion date November 30, 2011

Study information

Verified date July 2018
Source Novartis
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a prospective pilot study to evaluate the usability and applicability of a self monitoring test of visual function with the handheld Health Management Tool (HMT) to remotely monitor neovascular Age Related Macular Degeneration (AMD) to detect a potential change in disease status.


Recruitment information / eligibility

Status Completed
Enrollment 160
Est. completion date November 30, 2011
Est. primary completion date November 30, 2011
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients with CNV secondary to AMD and not other causes in at least one eye identified by the investigator to be eligible for ranibizumab treatment

- Patients with a BCVA letter score in the study eye is 24 or better using an ETDRS chart measured at 4 meters distance

Exclusion Criteria:

- Patients with any concurrent ocular condition that may result in visual loss during the study

- Patients with past (within the prior 6 months) or current use of, or likely need for, systemic medications that are known to be toxic to the lens, retina, or optic nerve

- Other protocol-defined inclusion/exclusion criteria may apply

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Health Management Tool (HMT)
Mobile computing platform (ie HMT) which allows subjects to perform home monitoring tests

Locations

Country Name City State
United States Novartis Investigative Site Beverly Hills California
United States Novartis Investigative Site Charlotte North Carolina
United States Novartis Investigative Site Cincinnati Ohio
United States Novartis Investigative Site Cleveland Ohio
United States Novartis Investigative Site Fort Myers Florida
United States Novartis Investigative Site Kingsport Tennessee
United States Novartis Investigative Site Largo Florida
United States Novartis Investigative Site Las Vegas Nevada
United States Novartis Investigative Site Lincoln Nebraska
United States Novartis Investigative Site Nashville Tennessee
United States Novartis Investigative Site New York New York
United States Novartis Investigative Site Omaha Nebraska
United States Novartis Investigative Site Rapid City South Dakota
United States Novartis Investigative Site Rochester New York
United States Novartis Investigative Site Sacramento California
United States Novartis Investigative Site San Antonio Texas
United States Novartis Investigative Site Sarasota Florida
United States Novartis Investigative Site Slingerlands New York
United States Novartis Investigative Site Springfield Illinois
United States Novartis Investigative Site Toms River New Jersey
United States Novartis Investigative Site Torrance California
United States Novartis Investigative Site West Mifflin Pennsylvania
United States Novartis Investigative Site Williamsburg Michigan

Sponsors (2)

Lead Sponsor Collaborator
Novartis Pharmaceuticals Carematix, VAS (Vital Art and Science)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Threshold value of handheld Health Management Tool (HMT) for choroidal neovascular AMD diagnosis at baseline 16 weeks
Primary Identification of clinically relevant worsening of visual function in the home self testing mVT scores baseline to 16 weeks
Secondary Correlation of the handheld Health Management Tool (HMT) home self testing on the days of site visits and the mVT assessments performed during the site visits for absolute values after 16 weeks
Secondary Correlation between the home deterioration signal and the monthly change in the handheld Health Management Tool (HMT) assessments performed during the site visits after 16 weeks
Secondary Patient compliance and reliability of performing the home self testing using the handheld Health Management Tool (HMT) after 16 weeks
Secondary Correlation between absolute values of the handheld Health Management Tool (HMT) and BCVA/ central retinal subfield thickness (CRST) 16 weeks
Secondary Correlation of the monthly changes in handheld Health Management Tool(HMT)to those of BCVA / OCT / Clinical examination after 16 weeks
Secondary Correlation of diagnosis of choroidal neovascular AMD with BCVA/ central retinal subfield thickness The disease diagnoses at baseline will be correlated to values of BCVA and CRST at baseline baseline
Secondary Correlation of monthly changes observed with thein the investigator judgment (CJ-C) to BCVA / OCT / Clinical examination Monthly changes in BCVA /OCT and clinical examination will be compared to clinical relevant changes as judged by the investigator on the CJC. baseline to 16 weeks
Secondary Patient compliance with the signs and symptom questionnaire The percentage of completed assessments of the signs & symptoms questionnaire on the HMT will be provided baseline to 16 weeks
Secondary Patient satisfaction regarding the use of the HMT 16 weeks
See also
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Enrolling by invitation NCT05481827 - ORACLE: A Long-term Follow-up Study to Evaluate the Safety of GT005 in Participants With Geographic Atrophy Secondary to Age-related Macular Degeneration Treated in a Gyroscope-sponsored Antecedent Study Phase 2
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