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Development of AD/OI after BS. for Orthostatic Intolerance
N/A
Recruiting
Led By Dhanunjaya Lakkireddy
Research Sponsored by Kansas City Heart Rhythm Research Foundation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 3 months
Awards & highlights
Study Summary
Observational two phase, retrospective and prospective registry study to assess the prevalence of and characterize outcomes of autonomic dysfunction (AD) in patients who undergo bariatric surgery (BS) and to better define the underlying pathophysiology of AD following BS.
Eligible Conditions
- Orthostatic Intolerance
- Autonomic Nervous System Disorders
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 3 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~3 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
To assess the prevalence of and characterize outcome of autonomic dysfunction (AD) in patients who undergo bariatric surgery (BS)
Trial Design
1Treatment groups
Experimental Treatment
Group I: Development of AD/OI after BS.Experimental Treatment1 Intervention
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Who is running the clinical trial?
Kansas City Heart Rhythm Research FoundationLead Sponsor
26 Previous Clinical Trials
11,572 Total Patients Enrolled
Kansas City Heart and Rhythm Institute, Overland Park, KSUNKNOWN
Bariatric and Metabolic Specialists, Overland Park, KSUNKNOWN
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