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NCT06289413 · ClinicalTrials.gov registry record
Autonomic Dysfunction in Patients Following Bariatric Surgery: The ADiPOSE Study
A clinical trial of Autonomic Dysfunction and Orthostatic Intolerance, sponsored by Kansas City Heart Rhythm Research Foundation.
- Recruiting
- Registry status
- 400
- Enrollment target
- 8
- Study locations
NCT06289413 is a study of Autonomic Dysfunction and Orthostatic Intolerance that is actively recruiting participants, run by Kansas City Heart Rhythm Research Foundation. The registered enrollment target is 400 participants, above the 72-participant average among 8 other Autonomic Dysfunction trials with a reported enrollment target (456% higher). The trial reports 8 study locations across 2 states.
The verdict
NCT06289413, a study of Autonomic Dysfunction and Orthostatic Intolerance, is actively recruiting participants, sponsored by Kansas City Heart Rhythm Research Foundation.
- RECRUITING
- Registry status
- 400 participants
- Enrollment target
- 8
- Study locations
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.
Conditions Studied
Interventions
- OTHER Development of AD/OI after BS
Study Locations (8)
Kansas
- Menorah Medical Center - Overland Park
- Bariatric and Metabolic Specialists - Overland Park
- Kansas City Heart Rhythm Institute - Roe Clinic - Overland Park
- Overland Park Regional Medical Center - Overland Park
Missouri
- Centerpoint Medical Center Clinic - Independence
- Centerpoint Medical Center - Independence
- Research Medical Center Clinic - Kansas City
- Research Medical Center - Kansas City
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 400 participants |
| Start Date | 2024-02-12 |
| Est. Completion | 2025-12 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06289413
The ClinicalTrials.gov registry entry for NCT06289413 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 400 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 72-participant average among 8 other Autonomic Dysfunction trials with a reported enrollment target (456% higher). The listed sponsor is Kansas City Heart Rhythm Research Foundation, which has 22 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Autonomic Dysfunction appearing as the primary indexed condition, and to 1 intervention - of which Development of AD/OI after BS is the first listed.
NCT06289413 reports 8 study locations spanning 2 distinct geographic areas - top geographies include Kansas, Missouri.
Frequently Asked Questions
What is clinical trial NCT06289413 about?
NCT06289413 is a clinical study titled "Autonomic Dysfunction in Patients Following Bariatric Surgery: The ADiPOSE 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 the current status of trial NCT06289413?
This trial is currently recruiting. The enrollment target is 400 participants. The study started on 2024-02-12. Estimated completion is 2025-12.
What conditions does trial NCT06289413 study?
This clinical trial studies the following conditions: Autonomic Dysfunction, Orthostatic Intolerance.
What interventions are being tested in trial NCT06289413?
The interventions under investigation include: Development of AD/OI after BS (OTHER).
Who is sponsoring clinical trial NCT06289413?
This trial is sponsored by Kansas City Heart Rhythm Research Foundation, which has 22 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06289413 being conducted?
This trial has 8 study locations across Kansas, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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