About this trial
The purpose of this study is to assess wether the SONDA visual field test is suitable for patients with a supra sellar tumour.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Diagnosed with a (supra)sellar tumor
Visual field loss based on the most recent SAP; False positive rate <15%; fixation losses <20%
Informed written consent
Disqualifiers
Neurological disorders
Eye disease not related to a (supra)sellar tumor
Trial population
Patients with a (supra)sellar tumour and healthy controls
Trial design
Case-control
Prospective
Treatments tested in this trial
SONDA
Diagnostic testPerimetry based visualfield analysis
Treatment groups
Trial outcomes
Primary outcomes
Convert validity
Difference (dB) between the predicted MD (SONDA) and the assessed MD (SAP), expressed as delta MD.
Test-retest reliability
The variability of the predicted MD (dB) between consecutive measurements in the same person.
Secondary outcomes
Experience
The experience of patients expressed in scores and descriptives based on a questionnaire: Questionnaire Standardized Oculomotor and Neuro-Ophthalmic Disorder Assessment
Sponsors and contacts
Click on the lead sponsor to view all of their trials.
This trial is not recruiting at the moment. You can still explore other options: