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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01744444
Other study ID # 2012.737
Secondary ID
Status Completed
Phase Phase 2
First received November 30, 2012
Last updated December 17, 2013
Start date November 2012
Est. completion date July 2013

Study information

Verified date December 2013
Source Hospices Civils de Lyon
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Interventional

Clinical Trial Summary

Different treatment trials have been published in acquired nystagmus in the last decade; gabapentin and memantine have been found to be efficient in treating pendular nystagmus in Multiple Sclerosis. The effects of treatments are measured on nystagmus velocity, amplitude, frequency and on visual acuity. None of the trials measured a functional visual score or oscillopsia score.

The aim of our study is to evaluate the effect of gabapentin and memantine on the mean velocity, amplitude and frequency of pendular nystagmus, as well as on oscillopsia, visual acuity and vision-specific health-related quality of life score, in 10 patients with multiple sclerosis. The primary object is to find out the best variable to evaluate the efficiency of nystagmus treatment and the secondary, to compare the efficiency of both gabapentin and memantine in a common population of patients.


Recruitment information / eligibility

Status Completed
Enrollment 10
Est. completion date July 2013
Est. primary completion date July 2013
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- All patients may have a clinically definite, laboratory-supported diagnosis of multiple sclerosis according to the Mac Donald criteria.

- All patients may present a chronic acquired pendular nystagmus due to MS, observed over a period of 6 months.

- All patients will be informed about the design and purpose of the study, and all will give their informed, written consent to the protocol, which may have been approved by the local ethics committee.

- Age: above 18

- Able to understand the instructions

- Having a health coverage

- Able to sit down for 1 hour

- Stable dosage of previous medications (beginning 3 weeks previously and terminating at the end of the trial duration), except for steroids, gabapentin or memantine.

Exclusion Criteria:

- Ophthalmological

- Other ophthalmological disorder that could impair corrected visual acuity (Maculopathy, Retinopathy…)

- Neurological

- Ongoing seizure

- Severe handicap that does not allow sitting down position for 1 hour

- Suicidal behavior or risk

- Treatment

- Under memantine or gabapentin medication (these medications should have been stopped for at least 1 week for gabapentin and 3 weeks for memantine)

- Under morphine, N-methyl-D-aspartate such as amantadine, ketamine or dextromethorphan

- Steroid medication for a current relapse (beginning 3 weeks previously and terminating at the end of the trial duration)

- Known hypersensitivity to memantine or gabapentin

- General

- Unstable medical state

- Patient with a galactose intolerance, a lapp lactase deficiency or glucose-galactose malabsorption

- Moderate renal failure (creatinine clearance < 50 mL/min on bioassay dated from less than one month)

- Recent heart infarction (<3months)

- Unstable congestive heart insufficiency

- Unstable arterial hypertension

- Leucopenia (<2500/mm3)

- Transaminase increase (>5 time normal values)

- Pregnancy (on questioning)

- Tutelage or any legal protection measure

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Memantine
Patients will be randomly assigned to start on either memantine or gabapentin. For tolerance reasons, each treatment begins with a progressive increasing dose and stops with a progressive decreasing dose. The duration of the period of last dose (8 to 11 days) will be chosen according to the investigator's availability to organize post-tests.
Gabapentin
Patients will be randomly assigned to start on either memantine or gabapentin. For tolerance reasons, each treatment begins with a progressive increasing dose and stops with a progressive decreasing dose. The duration of the period of last dose (8 to 11 days) will be chosen according to the investigator's availability to organize post-tests.

Locations

Country Name City State
France Hôpital Neurologique Unité de Neuro-Ophtalmologie Bron

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Velocity using eye movement recording at Day17-21 No
Primary Velocity using eye movement recording at Day34-42 No
Primary Velocity using eye movement recording at Day64-79 No
Primary Velocity using eye movement recording at Day81-100 No
Secondary Functional score on questioning at Day17-21, Day34-42, Day64-79, Day81-100 No
Secondary Subjective measure of oscillopsia at Day17-21, Day34-42, Day64-79, Day81-100 No
Secondary Far visual acuity at Day17-21, Day34-42, Day64-79, Day81-100 No