Autonomic Dysfunction in Patients Following Bariatric Surgery: The ADiPOSE Study
Status: Recruiting
Location: See all (8) locations...
Intervention Type: Other
Study Type: Observational
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.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 85
View:
• 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
Locations
United States
Kansas
Bariatric and Metabolic Specialists
RECRUITING
Overland Park
Kansas City Heart Rhythm Institute - Roe Clinic
RECRUITING
Overland Park
Menorah Medical Center
RECRUITING
Overland Park
Overland Park Regional Medical Center
RECRUITING
Overland Park
Missouri
Centerpoint Medical Center
RECRUITING
Independence
Centerpoint Medical Center Clinic
RECRUITING
Independence
Research Medical Center
RECRUITING
Kansas City
Research Medical Center Clinic
RECRUITING
Kansas City
Contact Information
Primary
Donita Atkins
datkins@kchrf.com
816-651-1969
Time Frame
Start Date: 2024-02-12
Estimated Completion Date: 2025-12
Participants
Target number of participants: 400
Treatments
Development of AD/OI after BS.
Related Therapeutic Areas
Sponsors
Collaborators: Bariatric and Metabolic Specialists, Overland Park, KS, Kansas City Heart and Rhythm Institute, Overland Park, KS
Leads: Kansas City Heart Rhythm Research Foundation