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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03030729
Other study ID # TLV-0025-16
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 14, 2017
Est. completion date January 14, 2018

Study information

Verified date January 2017
Source Notal Vision Ltd
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Comparison between retinal measurements, done by the RT (Retinal Thickness) imaging and a commercial OCT (Optical Coherence Tomography)


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date January 14, 2018
Est. primary completion date January 14, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. Ability and agreement to give informed consent (IC)

2. Diagnosis of AMD or DR in SE by OCT

3. Ability to undergo OCT scans

Exclusion Criteria:

1. AMD and DR in the same SE

2. Evidence of macular disease other than AMD or DME in SE

Study Design


Locations

Country Name City State
Israel Sorasky Medical Center Tel Aviv

Sponsors (1)

Lead Sponsor Collaborator
Notal Vision Ltd

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Comparison between retinal measurements, done by the RTOCT device and a commercial OCT 1 year
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