Sleep disordered breathing (SDB) is common in cardiovascular patients. Patients after cardiac
surgery will be screened for SDB with the ApnoeLink device at the beginning of cardiac
Rehabilitation and then after 3 weeks and 3 months.
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Full eligibility criteria for NCT02632162
Ages eligible for Study
Genders eligible for Study
Accepts Healthy Volunteers
cardiac surgery or orthopedic surgery <2 weeks
All locations for NCT02632162
Zürcher RehaZentrum Wald
Wald, Switzerland, 8636
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Tris trial is registered with FDA with number: NCT02632162. The sponsor of the trial is Zürcher RehaZentrum Wald and it is looking for 450 volunteers for the current phase.
Official trial title: Prevalence, Severity and Natural Course of Sleep Apnea After Cardiac Surgery
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