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Incidence and Effects of Sleep Apnea on Intracerebral Aneurysms

Incidence and Effects of Sleep Apnea on Intracerebral Aneurysms - IESA-Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02880059
Acronym
IESA
Enrollment
200
Registered
2016-08-26
Start date
2016-06-30
Completion date
2021-06-30
Last updated
2017-10-31

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

Conditions

Blood Pressure Medication, Comorbidities, Complications (Subarachnoid Hemorrhage), Intracranial Aneurysm Size, Sleep Apnea (Defined as Apnea Hypopnea Index > 5/h)

Keywords

Sleep Apnea, Aneurysm, Subarachnoid Hemorrhage, Blood Pressure.

Brief summary

Patients with intracerebral aneurysm will be screened for sleep apnea using out of center polysomnography/polygraphy. Baseline blood pressure and medication will be assessed. Patients will be followed for up to 5 years to examine the increase in aneurysm size, rupture rate and changes in medication.

Detailed description

Patient presenting to the outpatient center for neurological of neurosurgical management of intracerebral aneurysm will be recruited. Sleep apnea will be assessed by questionnaire and out of center polygraph/polysomnography. Medication, comorbidities and blood pressure will be recorded. Change in aneurysm size and blood pressure medication will be evaluated annually for up to 5 years. Frequency of subarachnoid hemorrhage and increase in aneurysm size will be assessed.

Interventions

DEVICECardiorepiratory Polygraphy

Sleep apnea screening by out-of-center polysomnography/polygraphy

Sponsors

University Hospital, Bonn
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Intracerebral aneurysm * Age \>= 18yrs. * Ability to give informed consent

Exclusion criteria

* Stroke within 3 month of study inclusion.

Design outcomes

Primary

MeasureTime frameDescription
Blood pressure medicationBaselineBlood pressure medication at baseline will be accessed.
Blood pressureBaselineBlood pressure on baseline visit will be accessed.

Secondary

MeasureTime frameDescription
Subarachnoid hemorrhage5 yearsRate of aneurysm rupture and subarachnoid hemorrhage will be accessed annually.
Increase in size of aneurysm5 years
Change in blood pressure medication5 yearsBlood pressure medication will be accessed on annual follow-up for up to 5 years.

Countries

Germany

Contacts

Primary ContactSebastian Zaremba, MD
zaremba.sebastian@gmx.net+49(0)228-287-16566
Backup ContactErdem Guersir, MD, PhD
erdem.gueresir@ukb.uni-bonn.de+49(0)228-287-16566

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026