Clinical Autonomic Disorders: A Training Protocol



Status:Recruiting
Conditions:Healthy Studies, Cardiology, Neurology, Neurology
Therapuetic Areas:Cardiology / Vascular Diseases, Neurology, Other
Healthy:No
Age Range:2 - Any
Updated:3/17/2019
Start Date:May 31, 2014
End Date:April 30, 2019
Contact:Janna Gelsomino, R.N.
Email:janna.gelsomino@nih.gov
Phone:(301) 435-5166

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Background:

- The autonomic nervous system helps control things that happen automatically in the body,
like blood pressure, heart rate, and digestion. When it doesn t work properly, it s called
dysautonomia. Researchers want to learn more about dysautonomias and train doctors to learn
how to better diagnose them.

Objectives:

- To allow people with autonomic disorders to be evaluated.

- To help fellows in the NIH Autonomic Disorders fellowship program see a variety of
diseases in their training.

Eligibility:

- People age 18 and older with dysautonomia; children over age 2 if they might benefit

- Healthy adult volunteers

Design:

- Participants will have different procedures depending on their symptoms. They will have
one or more visits. They will have some but not all of the tests below.

- Participants will have a medical history and physical exam. They may be tested for
problems thinking. They may complete a symptom questionnaire. They may have their
temperature and blood pressure taken.

- Participants may have an intravenous line placed. A needle will guide a thin plastic
tube into an arm vein.

- Participants may have blood drawn several times. They may give a urine sample.

- Participants may have an electrocardiogram.

- How much blood a participant s heart is pumping and/or how much blood is flowing through
their arm may be measured. The total amount of blood in their bloodstream may be
measured.

- Participants may have their ability to sweat and/or sense of smell tested.

- Breathing, bowel sounds, and/or body functions may be monitored.

- Pupil size, response to environmental temperature changes, and/or breathing may be
measured.

- Participants may have a bladder ultrasound.

- Small pieces of skin may be taken for study.

Objective:

This Protocol is to facilitate training of Fellows in evaluation of clinical disorders of the
autonomic nervous system. The training is necessary to enable Fellows to sit for and pass the
certifying examination in autonomic disorders administered by the United Council for
Neurologic Subspecialties (UCNS) and to maintain UCNS accreditation of the Fellowship. A
secondary objective is to include results of evaluations and testing with those from other
Protocols, for future data analyses.

Study population:

Referred patients with known or suspected abnormalities of one or more components of the
autonomic nervous system and healthy adult volunteers. Volunteers will be studied for Fellows
to practice and gain normative values for pupillometric function.

Design:

Clinical physiologic, neuropharmacologic, and neurochemical testing will be performed during
outpatient clinic visits or during inpatient admissions, depending on the individual testing
schedule. Inpatient testing may be done in conjunction with other Protocols (e.g.,
03-N-0004). Most of the testing under this Protocol can be completed in a single outpatient
visit over the course of a workday. Testing procedures under this Protocol will be performed
as needed for adequate Fellow training. In addition to autonomic medical history and physical
examination, clinical testing procedures may include (A) monitoring of hemodynamics,
sweating, and other physiologic parameters associated with the Valsalva maneuver,
orthostasis, or external temperature manipulation; (B) venous blood sampling for assays of
levels of catecholamines and related neurochemicals; (C) administration of autonomic test
drugs; (D) skin biopsies; (E) blood volume measurement; (F) pupillometry; (G)
gastrointestinal phonography; (H) urinary bladder ultrasound; and (I) neurobehavioral rating
scales.

Outcome measures:

The main outcome measure is competency in clinical and laboratory evaluation of autonomic
disorders, based on assessment of the Fellow by the Principal Investigator at approximately
6-month intervals. A secondary outcome measure is results obtained under this Protocol, which
may be analyzed and reported as research data along with data from other Protocols.

- INCLUSION CRITERIA - PATIENTS:

Patients may be included if they are at least 18 years old and are known or suspected to
have failure of one or more components of the autonomic nervous system, small fiber
neuropathy, inherited dysautonomia, orthostatic intolerance, neurocardiogenic syncope,
status post endoscopic thoracic sympathectomy, or disorders of catecholamine synthesis or
fate.

Children greater than two years old may be enrolled in this Protocol if they might
personally benefit from the tests in the Protocol through the establishment of a diagnosis.

EXCLUSION CRITERIA - PATIENTS:

There are no exclusion criteria for the study as a whole.

INCLUSION CRITERIA - HEALTHY VOLUNTEERS:

Healthy adult Volunteers (at least 18 years old) may be included, pending normal or
medically insignificant results of history and physical examination. A repeat history and
physical examination is required if more than 6 months have gone by from a previous workup.

EXCLUSION CRITERIA - HEALTHY VOLUNTEERS:

A candidate Healthy Volunteer will be excluded if the person has any of the following:
symptoms of autonomic dysfunction, including lightheadedness, fainting, abnormalities of
sweating, frequent nausea, vomiting, constipation, or diarrhea, or urinary frequency or
retention. If the Volunteer has a condition requiring medication that in the judgment of
the Investigators will affect results of the pupillometric tests under this Protocol, the
Volunteer may be included for training purposes.
We found this trial at
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9000 Rockville Pike
Bethesda, Maryland 20892
Phone: 800-411-1222
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