Method of Assessment of Driving Ability in Patients Suffering From Wakefulness Pathologies (AUTOSOP)

University Hospital of Bordeaux

Status: Completed

Conditions: Hypersomnia; Narcolepsy

Treatments: Drug: Modafinil; Drug: Placebo

Study type: Interventional

Funder types: Other

Identifiers

NCT00916253

CHUBX 2008/37

Details and patient eligibility

About

The project will improve scientific knowledge regarding a recent law applying potentially to every french driver. It will give for the first time an indication on the impact of alerting treatments on driving risks. It will reinforce the links between different research environments (sleep physiopathology, clinical research, cognitive neurosciences, driver's supervision, virtual reality, pharmacology) among the RESAT network (Réseau Eveil Sommeil Attention Transport). It will stimulate data acquisition in technological research to better understand the difference between real and simulated driving

Full description

Excessive daytime sleepiness is responsible of 20% of traffic accidents and 2/3 of truck accidents on French Freeways. Since the publication of a new law (arrêté du 28 décembre 2005 du journal officiel) regulating fitness to drive, the Maintenance of Wakefulness Test (MWT) is now mandatory to evaluate driving skills of patients suffering of excessive daytime sleepiness. The MWT has shown a good predictability of driving handicap on simulators in patients suffering from obstructive sleep apnea syndrome. Nevertheless no study has proven yet the predictability of the MWT regarding real and simulated driving in narcoleptics and hypersomniacs. Furthermore, even if alerting drugs significantly improve MWT scores there is no data available concerning the impact of these drugs on fitness to drive. This lack of knowledge is a major handicap to evaluate driving skills of treated patients suffering from excessive daytime sleepiness. The main objective of our project is to test the predictive value of the MWT on real and simulated driving performances in untreated and treated sleepy patients suffering from narcolepsy and hypersomnia. Inclusion of healthy volunteers will allow to collect reference data about somnolence during MWT.

Enrollment: 27 patients

Sex: All

Ages: 18 to 65 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria for Patients:

• Narcoleptic patients with or without cataplexy or hypersomniacs
• aged from 18 to 65 years,
• treated for attacks of cataplexy,
• treated with a maximum dose of Modiodal: 400 mg per day (4 tablets of 100mg),
• without any other disease which could be responsible of excessive daytime sleepiness,
• having their driver's licence,
• driving more than 5000 Km/year,
• registered to French national health and pensions organization,
• having regular timetables of life 7 days before beginning the study,
• having given their written light agreement in order to participate in the study.

Inclusion Criteria for Healthy Volunteers:

• without any sleep disorders,
• having their driver's licence since at least 2 years,
• driving more than 5000 Km/year,
• registered to French national health and pensions organization,
• having regular timetables of life 7 days before beginning the study,
• having given their written light agreement in order to participate in the study.

Exclusion Criteria for Patients:

• Night workers,
• breast-feeding or pregnant women
• Beck's scale score < 8,
• neurologic disease,
• cardiovascular disorders including cardiac arrhythmia,
• sleep disorders except narcolepsy and hypersomnia,
• pulmonary disorders,
• renal disorders,
• endocrinal disorders,
• having participated in a clinical study during the last 6 months,
• unable to drive.

Exclusion Criteria for Healthy Volunteers:

• Night workers,
• neurologic disease,
• cardiovascular disorders,
• sleep disorders,
• pulmonary disorders,
• renal disorders,
• endocrinal disorders,
• having participated in a clinical study during the last 6 months,
• unable to drive.

Trial design

Primary purpose: Diagnostic

Allocation: Randomized

Interventional model: Crossover Assignment

Masking: Double Blind

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27 participants in 3 patient groups

Modafinil First

Experimental group

Description:

Treatment by Modafinil during first condition then placebo during second condition

Treatment:

Drug: Placebo

Drug: Modafinil

Placebo First

Experimental group

Description:

Treatment by Placebo during first condition then Modafinil during second condition

Treatment:

Drug: Placebo

Drug: Modafinil

H

No Intervention group

Description:

Healthy Volunteers