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Clinical phenotypes and Precise Treatment of Adult OSA (Obstructive Sleep Apnea): A Multicenter Study

Clinical Phenotypes and Precise Treatment of Adult OSA: A Multicenter Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ONC-17013132
Enrollment
Unknown
Registered
2017-10-27
Start date
2017-01-01
Completion date
Unknown
Last updated
2017-11-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obstructive Sleep Apnea (OSA)

Interventions

CPAP Group:CPAP (Contious Positive Airway Pressure)

Sponsors

Beijing Tsinghua Changgung Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) untreated patients diagnosed with OSA; (2) agef between 18 and 75 years; (3) full night PSG showed both REM (rapid eye movement) stage and NREM (non-rapid eye movement) stage, and contained both supine position and lateral position, and the total supine-sleep time > 30min; (4) sleep efficiency = 75%. ;Inclusion criteria: (1) untreated patients diagnosed with OSA; (2) agef between 18 and 75 years; (3) full night PSG showed both REM (rapid eye movement) stage and NREM (non-rapid eye movement) stage, and contained both supine position and lateral position, and the total supine-sleep time > 30min; (4) sleep efficiency = 75%. ;Inclusion criteria: (1) untreated patients diagnosed with OSA; (2) agef between 18 and 75 years; (3) full night PSG showed both REM (rapid eye movement) stage and NREM (non-rapid eye movement) stage, and contained both supine position and lateral position, and the total supine-sleep time > 30min; (4) sleep efficiency = 75%. ;Inclusion criteria: (1) untreated patients diagnosed with OSA; (2) agef between 18 and 75 years; (3) full night PSG showed both REM (rapid eye movement) stage and NREM (non-rapid eye movement) stage, and contained both supine position and lateral position, and the total supine-sleep time > 30min; (4) sleep efficiency = 75%. ;Inclusion criteria: (1) untreated patients diagnosed with OSA; (2) agef between 18 and 75 years; (3) full night PSG showed both REM (rapid eye movement) stage and NREM (non-rapid eye movement) stage, and contained both supine position and lateral position, and the total supine-sleep time > 30min; (4) sleep efficiency = 75%.

Exclusion criteria

Exclusion criteria: hypothyroidism, vocal cord paralysis, acromegalis and any other disease causing secondary OSA, conscious disturbance, active psychiatric disease, central apnea, severe restrictive or obstructive pulmonary disease, neuromuscular disease, and significant craniofacial anomalies affecting airway.;Exclusion criteria: hypothyroidism, vocal cord paralysis, acromegalis and any other disease causing secondary OSA, conscious disturbance, active psychiatric disease, central apnea, severe restrictive or obstructive pulmonary disease, neuromuscular disease, and significant craniofacial anomalies affecting airway.;Exclusion criteria: hypothyroidism, vocal cord paralysis, acromegalis and any other disease causing secondary OSA, conscious disturbance, active psychiatric disease, central apnea, severe restrictive or obstructive pulmonary disease, neuromuscular disease, and significant craniofacial anomalies affecting airway.;Exclusion criteria: hypothyroidism, vocal cord paralysis, acromegalis and any other disease causing secondary OSA, conscious disturbance, active psychiatric disease, central apnea, severe restrictive or obstructive pulmonary disease, neuromuscular disease, and significant craniofacial anomalies affecting airway.;Exclusion criteria: hypothyroidism, vocal cord paralysis, acromegalis and any other disease causing secondary OSA, conscious disturbance, active psychiatric disease, central apnea, severe restrictive or obstructive pulmonary disease, neuromuscular disease, and significant craniofacial anomalies affecting airway.

Design outcomes

Primary

MeasureTime frame
AHI (Apnea Hypopnea Index);lowest oxygen saturation;mean oxygen saturation;CT90;minimum velopharyngeal cross-sectional area;minimum velopharyngeal transverse diameter;minimum velopharyngeal anteroposterior diameter;minimum glossopharyngeal cross-sectional area;minimum glossopharyngeal transverse area;minimum glossopharyngeal anteroposterior diameter;mandibule-hyroid distance;genitoglossal myoelectricity;C-reactive protein (CRP);FBG (fasting blood glucose);fasting insulin level;blood lipid level;Blood Pressure;Blood Pressure;serum uric acid (UA);survival time, mortality, disability rate;

Secondary

MeasureTime frame
ESS (Epworth Sleepiness Scale);The Quality of Life Scale (QOLS);

Countries

China

Contacts

Public ContactJingying Ye;Jingying Ye;Jingying Ye;Jingying Ye;Jingying Ye ;;;;

Beijing Tsinghua Changgung Hospital;Beijing Tsinghua Changgung Hospital;Beijing Tsinghua Changgung Hospital;Beijing Tsinghua Changgung Hospital;Beijing Tsinghua Changgung Hospital

yejingying@yeah.net;yejingying@yeah.net;yejingying@yeah.net;yejingying@yeah.net;yejingying@yeah.net+86 13701396970;+86 13701396970;+86 13701396970;+86 13701396970;+86 13701396970

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026