"Sleep- Apnoea Indian Registry (S-AIR)"
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Indian Chest Society
- Enrollment
- 1,500
- Locations
- 2
- Primary Endpoint
- Will create an Indian multi centred Sleep apnea database
Study Overview
Brief Summary
This registry is seeking to establish aregister of patients diagnosed with Sleep Apnoea (SA) in India in collaborationwith Indian Chest Society (ICS), AVISS HEALTH and Artemis Hospital, Gurgaon. Wewish to know more about how we treat SA and how many patients are there inINDIA with this condition. One way of doing this is to record information aboutpatients that are diagnosed with SA. As a part of this registry we will storesimple informations about enrolled pt’s age,the results of polysomnography tesst and the treatments that the pts havereceived. This will help us in describing the impact of SA on the pt, and onhealthcare in India. The data collected in the registry will help us toevaluate how well treatment works and help to design better clinical trials byunderstanding more about the disease.
Study Design
- Study Type
- Observational
Eligibility Criteria
- Ages
- 18.00 Year(s) to 70.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •1.A clinical history consistent with sleep apnea (excessive daytime sleepiness, hypopnea, apnea, altered sleep quality, morning headaches,daytime tiredness) 2.patient diagnosed with sleep apnea using Polysomnography(PSG)/Home Sleep Study test(level 1,2,3).
Exclusion Criteria
- •1.any other sleep related syndrome not overlapping with sleep apnea 2.Age <18 years 3.Delayed sleep syndrome 4.Patients who have not undergone Polysomnography test 5.Patients who are unable or unwilling to provide informed consent.
Outcomes
Primary Outcomes
Will create an Indian multi centred Sleep apnea database
Time Frame: 5 years
Secondary Outcomes
- Will create an Indian multi centred Sleep apnea database(5 years)