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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02078401
Other study ID # S56406
Secondary ID
Status Recruiting
Phase N/A
First received February 26, 2014
Last updated July 1, 2014
Start date April 2014

Study information

Verified date July 2014
Source Universitaire Ziekenhuizen Leuven
Contact Catherine Cassiman, MD
Phone 00321632660
Email catherine.cassiman@uzleuven.be
Is FDA regulated No
Health authority Belgium: Ethics Committee
Study type Observational

Clinical Trial Summary

The goal of this project is to get more insight into the (neuro)ophthalmological characteristics of children with neurofibromatosis type 1. This way investigators would like to update the current guidelines for follow up and treatment of optic pathway gliomas. Clinical findings will be compared with the results of Optical coherence tomography (OCT) and MRI (magnetic resonance imaging).


Recruitment information / eligibility

Status Recruiting
Enrollment 200
Est. completion date
Est. primary completion date August 2014
Accepts healthy volunteers No
Gender Both
Age group N/A to 18 Years
Eligibility Inclusion Criteria:

- neurofibromatosis type 1

Exclusion Criteria:

- no neurofibromatosis type 1

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Locations

Country Name City State
Belgium University Hospitals Leuven Leuven

Sponsors (1)

Lead Sponsor Collaborator
Universitaire Ziekenhuizen Leuven

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual acuity childhood (0 to 18y) No
Primary Presence of optic pathway glioma childhood (0 to18y) No
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