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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: Clinical Trial NA study, sponsored by Vanderbilt University Medical Center.
NCT00780390 is a NA study that was terminated before completion, run by Vanderbilt University Medical Center. The registered enrollment target is 10 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower). According to ClinicalTrials.gov, the official US trial registry.
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.
Primary Outcome
Electrical neurography data from sympathetic nerves
Interventions
- OTHER Autonomic Function Assessment
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 10 participants |
| Start Date | 2008-01 |
| Est. Completion | 2010-01 |
| Phase | NA |
Why NCT00780390 stopped before completion
NCT00780390 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (99% lower).
The record links to 0 conditions, and to 1 intervention - of which Autonomic Function Assessment is the first listed.
NCT00780390 does not publish any study locations in the registry export this page uses.
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.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00780390's enrollment target sits among peer trials
10 1927th of 2000 higher than 26 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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