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Clinical Trials/CTRI/2021/06/034461
CTRI/2021/06/034461
Not yet recruiting
未知

IVER STIFFNESS MEASUREMENT USING TRANSIENT ELASTOGRAPHY IN PATIENTS WITH OBSTRUCTIVE SLEEP APNEA

Overview

Phase
未知
Intervention
Not specified
Conditions
Not specified
Sponsor
ALL INDIA INSTITUTE OF MEDICAL SCIENCES RISHIKESH
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Observational

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Age \> 18 years.
  • 2\. Diagnosis of OSA based on International Classification of Sleep Disorders (ICSD) â?? 3 criteria:
  • ï?· Diagnosis requires (A\+B) or C:
  • A. The presence of one or more of the following:
  • 1\.The patient complains of sleepiness, nonrestorative sleep, fatigue, or insomnia symptoms.
  • 2\.The patient wakes with breath holding, gasping, or choking.
  • 3\.The bed partner or other observer reports habitual snoring, breathing interruptions, or both during the patientâ??s sleep.
  • 4\.The patient has been diagnosed with hypertension, a mood disorder, cognitive dysfunction, coronary artery disease, stroke, congestive heart failure, atrial fibrillation, or type 2 diabetes mellitus.
  • B. Polysomnography (PSG) or OCST demonstrates:
  • Five or more predominantly obstructive respiratory events (obstructive and mixed apneas, hypopneas, or respiratory effort related arousals \[RERAs]) per hour of sleep during a PSG or per hour of monitoring (OCST).

Exclusion Criteria

  • 1\.Age \<18 years
  • 2\.Causes of Chronic liver disease other than NAFLD
  • 3\.Patients with secondary causes of NAFLD such as drugs, jejunoileal bypass or extensive small bowel resection or total parenteral nutrition.
  • 4\. Patients who do not give consent

Outcomes

Primary Outcomes

Not specified

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