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Clinical Trial Summary

The purpose of the study is to evaluate the change in visual fields by means of automated static perimetry and to evaluate the change in retinal structure by means of spectral domain optical coherence tomography (SD-OCT) in adult patients with refractory complex partial seizures (CPS) being treated with vigabatrin (Sabril®)


Clinical Trial Description

Multicenter, prospective open-label study with approximately 25 sites in the US that specialize in caring for adult patients with refractory CPS

- Sites must have access to Humphrey static perimetry and to Spectralis SD-OCT.

- All vision test results will be sent to the central readers for evaluation.

- Additional study tests:

- The Columbia Suicide Severity Rating Scale (C-SSRS)

- The National Eye Institute Visual Field Questionnaire-39 (NEI VFQ-39)

- A whole blood sample for specific analysis of DNA characteristics

- An optional whole blood sample for exploratory analysis of DNA characteristics

- Plasma samples for bioanalytical analysis of vigabatrin and blood samples for taurine biomarker analysis ;


Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Supportive Care


Related Conditions & MeSH terms

  • Adult Refractory Complex Partial Seizures
  • Seizures

NCT number NCT01278173
Study type Interventional
Source Lundbeck LLC
Contact
Status Completed
Phase Phase 4
Start date December 2010
Completion date May 2015