Analysis of the metabolic syndrome improvement with the orexin receptor antagonist
Not Applicable
- Conditions
- Metabolic syndrome with insomnia
- Registration Number
- JPRN-UMIN000027445
- Lead Sponsor
- Kochi University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 0
Inclusion Criteria
Not provided
Exclusion Criteria
The patients appeared harmful effect of suvorexant The patients prescribed with CYP3A inhibitory drugs
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method We will evaluate whether the patients fill the criteria of MS 6 months after suvorexant treatment. MS criteria is satisfied with abdominal circumference is higher than 85cm in male and 90cm in female, and with higher than two items in follows: (1) Dyslipidemia: triglyceride is higher than 150mg/dl and/or HDL cholesterol is lower than 40mg/dl. (2) Hypertension: systolic blood pressure is higher than 130mmHg and/or diastolic blood pressure is higher than 85mmHg. (3) Impaired glucose tolerance: fasting blood glucose is higher than 110mg/dl.
- Secondary Outcome Measures
Name Time Method
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms link orexin receptor antagonism to metabolic syndrome and insomnia improvement?
How does orexin receptor antagonist efficacy compare to standard metabolic syndrome therapies like metformin or antihypertensives?
Which biomarkers correlate with response to orexin receptor antagonists in patients with metabolic syndrome and sleep disorders?
What are the potential adverse events of orexin receptor antagonists in metabolic syndrome treatment and their management strategies?
Are there combination therapies involving orexin receptor antagonists that enhance metabolic syndrome outcomes in clinical trials?