To estimate the potential clinical benefit from Tirzepatide among obese patients with moderate-severe OSA without DM Tirzepatide, moderate-severe OSA, OSA resolusion
Conditions
Interventions
Obese patient with moderate-severe OSA
Other
Sponsors
Sleep Center of Thammasat (SCENT)
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: 1. Age more than or equal to 18 years, 2. BMI more than or equal to 23 kg/m2, 3. Perform a sleep test due to suspected OSA
Exclusion criteria
Exclusion criteria: 1. Incomplete data
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To determine the proportion of patients who meet the criteria for the SURMOUNT-OSA study. - find the proportion of patients were eligible for SURMOUNT-OSA | — |
Secondary
| Measure | Time frame |
|---|---|
| To determine the proportion of moderate-to-severe OSA among patients with obesity. - proportion of obese in moderate-severe OSA,To compare clinical characteristics of patients with moderate-to-severe OSA and obesity, with and without comorbid type 2 diabetes. - compare characteristic between group,To predict number of patients who could achieve OSA resolution, reaching a level at which PAP therapy may no longer be recommended. - predict resolusion of OSA,To identify clinical predictors of OSA resolution. - identify clinical predictor | — |
Countries
Thailand
Contacts
Public ContactChatkarin Tepwimonpetkun
Thammasat University Hospital
Outcome results
None listed