Sleep Disordered Breathing in Transient Ischemic Attack (TIA)/Ischemic Stroke and Continuous Positive Airway Pressure (CPAP) Treatment Efficacy

NCT01097967 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 246

Last updated 2015-10-26

No results posted yet for this study

Summary

The study aims to observe the short term effect (3-month) of sleep disordered breathing (SDB) on cardiovascular parameters, heart rate variability, endothelial function and surrogate markers of atherosclerosis after acute cerebrovascular events (ACE). The long-term effect (6-24-month) of Continuous Positive Airway Pressure (CPAP) on clinical vascular outcome, cardiovascular parameters, evolution of surrogate of atherosclerosis heart rate variability and endothelial function after ACE is observed over 24 months. A preventive effect of CPAP therapy on cerebro-vascular events in patients with moderate-severe obstructive SDB without sleepiness after ictus or transient ischaemic attack will be evaluated.

Conditions

Interventions

OTHER

CPAP

Sponsors & Collaborators

  • Swiss National Science Foundation

    collaborator OTHER
  • Schweizerische Herzstiftung

    collaborator OTHER
  • ResMed

    collaborator INDUSTRY
  • Philips Respironics

    collaborator INDUSTRY
  • Prof. Claudio Bassetti

    lead OTHER_GOV

Principal Investigators

  • Claudio Bassetti, Professor · Universitätsspital Bern (Inselspital) und Universität Bern

  • Carlo Cereda, Capo CLinica · Neurocentre of Southern Switzerland, Ospedale Civico

  • Sebastian Ott, MD · Pneumology, University Hospital, Bern

  • Lino Nobili, Prof. MD · Neurology, Stroke Unit, Ospedale Niguarda, Milan, Italy

  • Mauro Manconi, MD · Neurocentre of Southern Switzerland, Ospedale Civico

  • Peter Young, Prof. MD · Universitätsklinik Münster, Zentrum für Schlafmedizin

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
35 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-07-31
Primary Completion
2016-04-30
Completion
2016-04-30

Countries

  • Germany
  • Italy
  • Switzerland

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01097967 on ClinicalTrials.gov