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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: Recruiting study of Autonomic Dysfunction and Orthostatic Intolerance, sponsored by Kansas City Heart Rhythm Research Foundation.

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. According to ClinicalTrials.gov, the official US trial registry.

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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.

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

FieldValue
Enrollment Target 400 participants
Start Date 2024-02-12
Est. Completion 2025-12

What NCT06289413 shows while recruiting

NCT06289413 is an observational study that tracks outcomes without assigning an intervention. The registered 400 participants enrollment target is mid-sized for trials with a published cap, above the 72-participant average among 8 other Autonomic Dysfunction trials with a reported enrollment target (456% higher).

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 lists 8 locations in 2 states (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.

Similar trials for Autonomic Dysfunction

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06289413's enrollment target sits among peer trials

400 1st of 8 higher than 8 of 8 other Autonomic Dysfunction trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Autonomic Dysfunction trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06289413, the US trial registry maintained by the National Library of Medicine. NCT06289413 (mid enrollment · multi site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.