A Study of the Structure and Function of the Retina in Adult Patients With Refractory Complex Partial Seizures Treated With Vigabatrin (Sabril®)
This study is ongoing, but not recruiting participants.
Information provided by (Responsible Party):
First received: January 14, 2011
Last updated: March 17, 2015
Last verified: March 2015
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®)
Adult Refractory Complex Partial Seizures
||Endpoint Classification: Safety Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Supportive Care
||A Prospective, Open-label Study of the Structure and Function of the Retina in Adult Patients With Refractory Complex Partial Seizures Treated With Vigabatrin (Sabril®)
Primary Outcome Measures:
- Change from reference value in field width as measured by 30-2 SITA Fast in field sensitivity (Mean Deviation - MD in dB) [ Time Frame: Baseline (Month 0), Month 3, Month 6, Month 9, Month 12 ] [ Designated as safety issue: Yes ]
- Change from reference value in average RNFL thickness (µm) as measured by SD-OCT [ Time Frame: Baseline (Month 0), Month 3, Month 6, Month 9, Month 12 ] [ Designated as safety issue: Yes ]
Potential changes in retinal function, as assessed by static perimetry, tangent corner test, visual acuity and color vision, during the first year of exposure to Sabril will be correlated with clinical changes in average retinal nerve fiber layer thickness (RNFL), as assessed by SD-OCT.
| Estimated Enrollment:
| Study Start Date:
| Estimated Primary Completion Date:
||September 2015 (Final data collection date for primary outcome measure)
Sabril: 500 mg tablets, orally. Physicians will dose their patients according to guidance provided in the product label.
Other Name: Vigabatrin
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
|Ages Eligible for Study:
||18 Years and older
|Genders Eligible for Study:
|Accepts Healthy Volunteers:
Important Inclusion Criteria:
- The patient speaks English or Spanish.
- The patient has had no prior exposure to Sabril.
- To begin Sabril therapy for the treatment of CPS.
- Male or female ≥18 years of age.
The patient has refractory CPS:
- The patient has complex partial epilepsy of more than 1 year duration and no other seizure type within the past year except for partial seizures secondarily generalized.
- The patient has failed because of lack of efficacy 3 or more prior or concurrent treatment trials including 3 or more anti-epileptic drugs (AEDs) of differing pharmacologic mechanisms administered as monotherapy or polytherapy.
- The patient is taking at least 1 AED. A vagal nerve stimulator is not counted as an AED.
- The patient reports an average of 2 or more seizures per month averaged over the prior 3 months.
- The patient is deemed by the treating neurologist and ophthalmologist to be able to reliably complete perimetry testing.
- The initial (Visit 1) SD-OCT and static perimetry readings tests must be performed and assessed for technical adequacy by the SD-OCT and perimetry central readers prior to the first dose of Sabril. The initial (Visit 1) tangent corner test must be performed prior to the first dose of Sabril.
- Prior exposure to Sabril.
- Pre-existing ocular or neurological disease that might affect bilateral visual fields or interfere with perimetry (e.g., aphakia, visually significant cataract, glaucoma, diabetes mellitus, ischemic optic neuropathy, multiple sclerosis). Patients with stable visual field defects from CNS lesions (e.g., epilepsy surgery more than 6 months prior to receiving Sabril) may be enrolled.
- Concurrent exposure to medications with known or suspected retinal or optic nerve toxicity.
- Concurrent use of an investigational agent or device or such use within 30 days of entering the study.
- Concurrent use of the ketogenic or similar diet.
- For any reason, the patient is considered by the investigator to be an unsuitable candidate for the study.
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To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below.
For general information, see Learn About Clinical Studies.
Please refer to this study by its ClinicalTrials.gov identifier: NCT01278173
||Email contact via H. Lundbeck A/S
No publications provided
History of Changes
|Other Study ID Numbers:
|Study First Received:
||January 14, 2011
||March 17, 2015
||United States: Food and Drug Administration
Keywords provided by Lundbeck LLC:
Vigabatrin-associated vision change
Adult refractory complex partial seizures
Central Nervous System Diseases
Nervous System Diseases
Additional relevant MeSH terms:
ClinicalTrials.gov processed this record on April 16, 2015
Central Nervous System Diseases
Nervous System Diseases
Signs and Symptoms
Central Nervous System Agents
Molecular Mechanisms of Pharmacological Action
Physiological Effects of Drugs