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Comparison of RT in Patients With Sleep Apnea With and Without Complaints of Daytime Sleepiness

F

Federal University of São Paulo

Status

Unknown

Conditions

Sleep Apnea

Study type

Observational

Funder types

Other

Identifiers

NCT01562262
CEP1122/11

Details and patient eligibility

About

Not all patients with the Obstructive Sleep Apnea Syndrome (OSAS), mostly mild, have excessive daytime sleepiness. Sleep fragmentation provides the performance decrease with increasing reaction time to external stimuli and correlates with excessive sleepiness. So, the study aims at assessing the effect of sleep fragmentation on the Reaction Time and it's maintenance in patients with OSAS compared with healthy, to better clarify were patients with and without somnolence differ. For that, will be recruited 30 male volunteers aged between 20 and 50 year old to participate in the study. They will be distributed in three groups: "CONTROL" (without symptoms of sleepiness and apnea and hypopnea index (AHI) less than 5), "SS" (with AHI between 5 and 15 without symptoms of somnolence) and group "CS" (with AHI between 5 and 15 with symptoms of somnolence). The groups will undergo a polysomnography and subsequently, the Test and Maintenance of Wakefulness and PVT Battery Tests. The reaction time will be compared, as well as the ability to keep the reaction time over time between groups to see whether there is a difference between the motor performance throughout the day and the perception of sleepiness.

Enrollment

30 estimated patients

Sex

Male

Ages

20 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Man
  • Aged between 20 and 45 years old
  • BMI between 20-30

Exclusion criteria

  • Cigarette Smoke
  • Drug intake
  • Other sleep disturbances

Trial design

30 participants in 3 patient groups

CTR
Description:
Control group
ASS
Description:
Apnea without complaints group
ACS
Description:
SAOS Group

Trial contacts and locations

1

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Central trial contact

Amaury T Barreto, Bsc

Data sourced from clinicaltrials.gov

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