Determining Disease Activity Biomarkers in Individuals With Polyarteritis Nodosa
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Purpose
Polyarteritis nodosa (PAN) is a rare immune system disorder that causes swelling and damage to small- and medium-sized blood vessels in the body. In order to properly treat this disease, it is critical that the level of disease activity can be determined over the course of the disease. The purpose of this study is to determine new biological markers, or biomarkers, that may be used to assess the severity of disease in people with PAN.
| Condition |
|---|
|
Polyarteritis Nodosa |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Longitudinal Protocol of Polyarteritis Nodosa |
Blood (serum and plasma), urine, and DNA
| Estimated Enrollment: | 150 |
| Study Start Date: | April 2006 |
| Estimated Study Completion Date: | April 2016 |
| Estimated Primary Completion Date: | April 2016 (Final data collection date for primary outcome measure) |
PAN, also known as systemic necrotic vasculitis, was the first recognized form of primary systemic vasculitis. PAN causes the inflammation of small- to medium-sized blood vessels, especially those supplying the nerves, skin, kidneys, gastrointestinal tract, heart, eye, and genitals. Unlike another form of vasculitis called microscopic polyangiitis, PAN does not usually cause glomerulonephritis, a type of kidney disease, or vasculitis in the very smallest blood vessels (arterioles, capillaries, and venules). There are no radiographic or serologic tests that can reliably measure disease activity in PAN. Currently, clinicians must rely on patients' symptoms, signs, laboratory tests, and imaging to guide treatment decisions, but such data are rarely consistently reliable in determining PAN disease activity. This study will use new scientific methods to discover new biomarkers that can be used to monitor disease activity in PAN patients. These biomarkers may be used to help direct clinical care for PAN patients and assist in future drug development.
Study visits will occur monthly for the first year, then every 3 months thereafter for the remainder of the study. Blood and urine collection will occur at every visit. A physical exam and medical and medication history will occur every 3 months; also, participants will be asked to complete several questionnaires to assess disease activity, health status, and tobacco, alcohol, and drug use. Participants may have additional study visits if a disease flare or disease-related complications occur during the study.
Eligibility| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Individuals with polyarteritis nodosa. Enrollment will be sequential and participants will have disease in various stages and of different duration.
Inclusion Criteria:
- Parent or guardian willing to provide informed consent, if applicable
- Diagnosis of vasculitis
- Diagnosis of PAN, meeting at least 1 major criterion and 1 minor criterion OR 2 major criteria of the following adapted American College of Rheumatology (ACR) criteria that fall under the diagnosis of PAN and that are not explained by other causes:
MAJOR CRITERIA
- Arteriographic abnormality
- Presence of granulocyte or mixed leukocyte infiltrate in an arterial wall on biopsy
- Mononeuropathy or polyneuropathy
MINOR CRITERIA
- Weight loss of more than 4 kg (8.8 lbs)
- Livedo reticularis, cutaneous ulcerations, or skin nodules
- Testicular pain or tenderness
- Myalgias
- Diastolic blood pressure greater than 90 mm Hg
- Elevated blood urea nitrogen (BUN) or serum creatinine levels
- Ischemic abdominal pain
Exclusion Criteria:
- Microscopic polyangiitis
- Granulomatosis with polyangiitis(Wegener's)
- Churg-Strauss syndrome
- Takayasu's arteritis
- Giant cell arteritis
- Cogan's syndrome
- Behcet's disease
- Sarcoidosis
- Kawasaki's disease
- Cryoglobulinemic vasculitis
- Systemic lupus erythematosus
- Rheumatoid arthritis
- Mixed connective tissue disease or any overlap autoimmune syndrome
- Presence of antiproteinase 3 or antimyeloperoxidase antineutrophil cytoplasmic antibodies (ANCA)
- Glomeronephritis
- Alveolar hemorrhage
- Hepatitis B, hepatitis C, or HIV infection
- Any other infectious form of medium vessel vasculitis
- Isolated cutaneous PAN
Contacts and Locations| United States, Maryland | |
| The Johns Hopkins Vasculitis Center | Active, not recruiting |
| Baltimore, Maryland, United States, 21224 | |
| United States, Massachusetts | |
| Boston University School of Medicine | Recruiting |
| Boston, Massachusetts, United States, 02118 | |
| Contact: Daniel Finkel 617-414-2509 | |
| Principal Investigator: Paul A. Monach, MD, PhD | |
| United States, Minnesota | |
| Mayo Clinic College of Medicine | Recruiting |
| Rochester, Minnesota, United States, 55905 | |
| Contact: Jane Jaquith jaquith.jane@mayo.edu | |
| Principal Investigator: Steven R. Ytterberg, MD | |
| United States, Ohio | |
| Cleveland Clinic Foundation | Recruiting |
| Cleveland, Ohio, United States, 44195 | |
| Contact: Katie Gartner 216-445-1397 gartnek@ccf.org | |
| Principal Investigator: Carol A. Langford, MD, MHS | |
| United States, Pennsylvania | |
| University of Pennsylvania | Recruiting |
| Philadelphia, Pennsylvania, United States, 19104 | |
| Contact: Alex Giardino 215-614-4407 Alexandra.Giardino@uphs.upenn.edu; | |
| Principal Investigator: Peter Merkel, MD, MPH | |
| University of Pittsburgh | Recruiting |
| Pittsburgh, Pennsylvania, United States, 15260 | |
| Contact: Dawn McBride, RN 412-586-3545 dlmc@pitt.edu | |
| Principal Investigator: Larry Moreland, MD | |
| United States, Utah | |
| University of Utah | Recruiting |
| Salt Lake City, Utah, United States, 84112 | |
| Contact: Julieanne Nielsen 801-585-0798 Julieanne.Nielsen@hsc.utah.edu | |
| Principal Investigator: Curry Koening, MD, MHS | |
| Canada, Ontario | |
| St. Joseph's Healthcare | Recruiting |
| Hamilton, Ontario, Canada | |
| Contact: Sandra Messier 905-522-1155 ext 35873 smessier@stjoes.ca | |
| Principal Investigator: Nader A. Khalidi, MD | |
| Mount Sinai Hospital | Recruiting |
| Toronto, Ontario, Canada, M5T 3L9 | |
| Contact: Julia Farquharson 416-586-8616 JFarquharson@mtsinai.on.ca | |
| Principal Investigator: Simon Carette, MD | |
| Study Chair: | Peter A. Merkel, MD, MPH | University of Pennsylvania |
More Information
Additional Information:
Publications:
| Responsible Party: | Peter Merkel, Professor, University of Pennsylvania |
| ClinicalTrials.gov Identifier: | NCT00315406 History of Changes |
| Other Study ID Numbers: | RDCRN 5504, U54AR057319 |
| Study First Received: | April 14, 2006 |
| Last Updated: | October 23, 2012 |
| Health Authority: | United States: Federal Government |
Keywords provided by University of Pennsylvania:
|
PAN Periarteritis Nodosa |
Additional relevant MeSH terms:
|
Polyarteritis Nodosa Arteritis Vascular Diseases Cardiovascular Diseases |
Vasculitis Systemic Vasculitis Skin Diseases, Vascular Skin Diseases |
ClinicalTrials.gov processed this record on June 18, 2013