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Inter-individual differences after continuous positive airway pressure (CPAP) withdrawal in mild sleep apnoea patients, evaluated by their performance on a simulated driving task – A role for modafinil?

Inter-individual differences after continuous positive airway pressure (CPAP) withdrawal in mild sleep apnoea patients, evaluated by their performance on a simulated driving task – A role for modafinil?

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12606000005550
Enrollment
20
Registered
2006-01-04
Start date
2006-01-01
Completion date
Unknown
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

This double-blind, placebo-controlled study will examine the efficacy of modafinil to counteract possible daytime sleepiness after one night of CPAP withdrawal in long-term CPAP users. Sleep-wake activity on CPAP use will be assessed for 5 days using actigraphy. On the 5th night subjects will withdrew from CPAP treatment and use a nasal airflow device as a substitute. The following morning, subjects will report to the laboratory and received modafinil (200 mg). EEG will be assessed continuousl

This double-blind, placebo-controlled study will examine the efficacy of modafinil to counteract possible daytime sleepiness after one night of CPAP withdrawal in long-term CPAP users. Sleep-wake activity on CPAP use will be assessed for 5 days using actigraphy. On the 5th night subjects will withdrew from CPAP treatment and use a nasal airflow device as a substitute. The following morning, subjects will report to the laboratory and received modafinil (200 mg). EEG will be assessed continuously and then a 30 min driving simulation task (STISIM TM) will be completed 2 hours post drug administration. After a washout period of 14 days, subjects will repeat the protocol, receiving the other study medication.

Sponsors

Woolcock Institute of Medical Research
Lead SponsorOther

Study design

Allocation
Non-randomised trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
Male
Age
30 Years to 60 Years
Healthy volunteers
No

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026