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NCT00780390 · ClinicalTrials.gov registry record · NA

Autonomic Dysfunction and Spinal Cord Stimulation in Complex Regional Pain Syndrome

A NA study, sponsored by Vanderbilt University Medical Center.

Terminated
Registry status
NA
Development phase
10
Enrollment target

NCT00780390 is a NA study that was terminated before completion, run by Vanderbilt University Medical Center. The registered enrollment target is 10 participants.

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The verdict

NCT00780390, a NA study, was terminated before completion, sponsored by Vanderbilt University Medical Center.

TERMINATED
Registry status
NA
Development phase
10 participants
Enrollment target

Study Summary

To demonstrate that spinal cord stimulator has an effect on sympathetic function (the one that give us the fight and flight response). Therefore, if the spinal cord stimulator has an effect on sympathetic function, the responses from CRPS patients to different stimuli will differ significantly pre and post SCS implant. If CRPS patients exhibit autonomic, CRPS patients could be stratified according to their sympathetic function pre-implant. It is expected that patients with a moderate/mild form of autonomic dysfunction will have better outcomes with the SCS.

Interventions

  • OTHER Autonomic Function Assessment

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2008-01
Est. Completion 2010-01
Phase NA

What the Registry Record Tells You About NCT00780390

The ClinicalTrials.gov registry entry for NCT00780390 describes a study currently listed as terminated, categorized as NA. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vanderbilt University Medical Center, which has 677 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Autonomic Function Assessment is the first listed.

NCT00780390 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00780390 about?

NCT00780390 is a clinical study titled "Autonomic Dysfunction and Spinal Cord Stimulation in Complex Regional Pain Syndrome". To demonstrate that spinal cord stimulator has an effect on sympathetic function (the one that give us the fight and flight response). Therefore, if the spinal cord stimulator has an effect on sympathetic function, the responses from CRPS patients to different stimuli will differ significantly pre a...

What is the current status of trial NCT00780390?

This trial is currently terminated. It is a NA study. The enrollment target is 10 participants. The study started on 2008-01. Estimated completion is 2010-01.

What interventions are being tested in trial NCT00780390?

The interventions under investigation include: Autonomic Function Assessment (OTHER).

Who is sponsoring clinical trial NCT00780390?

This trial is sponsored by Vanderbilt University Medical Center, which has 677 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.