Autonomic Dysfunction in Patients Following Bariatric Surgery: The ADiPOSE Study
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-85
SponsorKansas City Heart Rhythm Research Foundation
About this trial
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.
Eligibility criteria
Qualifiers
Between the age of 18 - 85 years
Can provide consent
Negative urine B-hCG
Continued follow-up with the bariatric surgery team.
Disqualifiers
Unable to provide consent
Pregnant or breastfeeding
BMI < 35
Revision surgery of one of the following BS from above
Trial design
Treatments tested in this trial
- Development of AD/OI after BS
Treatment groups
400 Participants
are divided into 1 treatment groupSponsors and collaborators
Kansas City Heart Rhythm Research Foundation
Lead sponsor
Kansas City Heart Rhythm Institute
Collaborator
Bariatric and Metabolic Specialists, Overland Park, KS
Collaborator
Source ClinicalTrials.gov