Home › Primary Dysautonomias › NCT06289413
Autonomic Dysfunction in Patients Following Bariatric Surgery: The ADiPOSE Study
RecruitingObservational study
Who can join
Ages 18 to 85 · All sexes
Full eligibility criteria
Inclusion Criteria: * Between the age of 18 - 85 years * Can provide consent * Negative urine B-hCG * Continued follow-up with the bariatric surgery team. * BS includes one of the following: gastric bypass, sleeve gastrectomy, and biliopancreatic diversion with duodenal switch. * Phase I: Underwent BS within the last 3 years * Phase II: Will undergo BS within the next 3 months or underwent BS in the last 30 days Exclusion Criteria: * Unable to provide consent * Pregnant or breastfeeding * BMI \< 35 * Revision surgery of one of the following BS from above * Prior history of autonomic dysfunction prior to BS * Developed AD 72 months post-procedure * No evidence of AD/OI
About the study
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.
What is being tested
- Development of AD/OI after BS (other)
Sponsor: Kansas City Heart Rhythm Research Foundation · Participants: 400 · Started: Feb 12, 2024
Contact the study team
- Donita Atkins · Phone: 816-651-1969
Official record on ClinicalTrials.gov — NCT06289413
Locations in the U.S.
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.