Ischaemic Stroke and Sleep Apnea in Northern Part of Finland

NCT ID: NCT01861275

Last Updated: 2016-05-24

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

256 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-04-30

Study Completion Date

2015-01-31

Brief Summary

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Obstructive sleep apnoea is a risk factor for ischaemic stroke. study hypothesis: In prospective study the investigators want to know how many ischaemic stroke patients have sleep apnoea and does thrombolysis play a role in severity of osa in six months follow up.

Detailed Description

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In prospective study the investigators include all over 18 years old patients who came to emergency room for ischaemic stroke. Exclusion criteria is not able to co-operate or need for intensive care unit.The investigators shall take 100 control patients who have ischaemic stroke and no thrombolysis and 100 study patients who will have thrombolysis. The investigators do sleep registration during hospital staying within 2 days after patients have felt ill.Follow-up registration will be done after 6 months at home.

Conditions

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Sleep Apnoea Cerebral Palsy

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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Nasal CPAP

We want to study the nasal-cpap treatment and it's compliance in sleep apnea patients with ischaemic stroke.

Nasal CPAP

Intervention Type DEVICE

Nasal CPAP treatment for obstructive sleep apnoea

no Nasal CPAP

No nasal-cpap in sleep apnea patients with ischaemic stroke.

No interventions assigned to this group

Interventions

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Nasal CPAP

Nasal CPAP treatment for obstructive sleep apnoea

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* over 18 years old patients that have cerebral palsy and are able to participate to the study.

Exclusion Criteria

* no co-operation and need for intensive care unit
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Oulu

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Tarja Saaresranta, Md PhD

Role: STUDY_DIRECTOR

University hospital of Turku

Locations

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Oulu university hospital,department of neurology

Oulu, Northern Finland, Finland

Site Status

Countries

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Finland

References

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Huhtakangas JK, Saaresranta T, Vahanikkila H, Huhtakangas J. Nocturnal hypoxemia and central apneas increase mortality, but not recurrent ischemic events after ischemic stroke. Sleep Med. 2022 Sep;97:1-9. doi: 10.1016/j.sleep.2022.05.014. Epub 2022 May 23.

Reference Type DERIVED
PMID: 35679775 (View on PubMed)

Huhtakangas JK, Huhtakangas J, Bloigu R, Saaresranta T. Unattended sleep study in screening for sleep apnea in the acute phase of ischemic stroke. Sleep Med. 2020 Jan;65:121-126. doi: 10.1016/j.sleep.2019.08.002. Epub 2019 Aug 8.

Reference Type DERIVED
PMID: 31751906 (View on PubMed)

Huhtakangas JK, Saaresranta T, Bloigu R, Huhtakangas J. The Evolution of Sleep Apnea Six Months After Acute Ischemic Stroke and Thrombolysis. J Clin Sleep Med. 2018 Dec 15;14(12):2005-2011. doi: 10.5664/jcsm.7524.

Reference Type DERIVED
PMID: 30518443 (View on PubMed)

Huhtakangas JK, Huhtakangas J, Bloigu R, Saaresranta T. Prevalence of sleep apnea at the acute phase of ischemic stroke with or without thrombolysis. Sleep Med. 2017 Dec;40:40-46. doi: 10.1016/j.sleep.2017.08.018. Epub 2017 Oct 7.

Reference Type DERIVED
PMID: 29221777 (View on PubMed)

Other Identifiers

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36/2013

Identifier Type: OTHER

Identifier Source: secondary_id

36/2013 UO

Identifier Type: OTHER

Identifier Source: secondary_id

36/2013

Identifier Type: -

Identifier Source: org_study_id

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