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Effect of Sleep Apnea on Blood Pressure Control and Outcome Early After Subarachnoid Hemorrhage

U

University Hospital Bonn (UKB)

Status

Unknown

Conditions

Subarachnoid Hemorrhage
Sleep Apnea

Treatments

Device: Sleep Apnea Screening (Out of Center Polysomnography Device)

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

In this observational study patients with subarachnoid hemorrhage (SAH) will be screened for sleep apnea (SA) to investigate if SA is associated with impaired blood pressure control and worse clinical outcome early after SAH.

Full description

Patients admitted with non-traumatic SAH will be consented and screened for sleep apnea within 48 hours after hospital admission. Blood pressure and clinical outcome will be monitored throughout ICU treatment and hospital stay, respectively. Diagnosis of sleep apnea will be confirmed on follow-up 3-6 month after SAH by sleep apnea screening (portable cardiorespiratory monitoring and out-of-center polysomnography, respectively).

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Subarachnoid Hemorrhage (Hunt & Hess 1 to 4)
  • > 18 years of age
  • Ability to consent for study of healthcare proxy able to confirm patient will to participate

Exclusion criteria

  • Stoke within 3 month prior to admission
  • Intubation prior or within 24 hours after admission
  • no healthcare proxy

Trial design

200 participants in 2 patient groups

Patients with Sleep Apnea
Description:
Patients with increased apnea-hypopnea-index (\>5/h)
Treatment:
Device: Sleep Apnea Screening (Out of Center Polysomnography Device)
Patients without Sleep Apnea
Description:
Patients with normal apnea-hypopnea-index (5/h and below)
Treatment:
Device: Sleep Apnea Screening (Out of Center Polysomnography Device)

Trial contacts and locations

1

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Central trial contact

Sebastian Zaremba, MD; Erdem Gueresir, MD, PhD

Data sourced from clinicaltrials.gov

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