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Juvenile Idiopathic Arthritis (JIA) Registry
NCT00783510 · View on ClinicalTrials.gov ↗
Study Summary
This is a global registry, to evaluate the long-term safety of Humira® in patients with moderate to severe polyarticular Juvenile Idiopathic Arthritis (JIA), that are treated as recommended in the Humira® product label. Patients treated with MTX will be considered a reference group. Patients will be followed in both the Humira® and Methotrexate (MTX) arms for 10 years from the enrollment date into one of the treatment arms.
Conditions Studied
Interventions
- DRUG Methotrexate
- BIOLOGICAL adalimumab
Study Locations (20)
Illinois
- Ann & Robert H Lurie Children's Hospital of Chicago /ID# 20966 — Chicago
- The University of Chicago Medical Center /ID# 21981 — Chicago
- Methodist Medical Group Rheum /ID# 46343 — Peoria
New York
- North Shore University Hospital /ID# 21022 — New Hyde Park
- University of Rochester Medical Center /ID# 20967 — Rochester
- New York Medical College /ID# 21964 — Valhalla
Arizona
- AZ Arthritis and Rheumotology Research, PLLC /ID# 21023 — Phoenix
- Catalina Pointe Clinical Research /ID# 40227 — Tucson
Arkansas
- Arkansas Children's Hospital /ID# 23505 — Little Rock
California
- Children's Hospital Los Angeles /ID# 24386 — Los Angeles
District of Columbia
- Children's National Medical Center /ID# 23506 — Washington D.C.
Florida
- Duplicate_Arthritis Associates South FL /ID# 17001 — Delray Beach
Indiana
- Indiana University /ID# 11421 — Indianapolis
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 849 participants |
| Start Date | 2008-07-11 |
| Est. Completion | 2024-02-01 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT00783510
The ClinicalTrials.gov registry entry for NCT00783510 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 849 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is AbbVie, which has 603 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 2 conditions, with Juvenile Idiopathic Arthritis appearing as the primary indexed condition, and to 2 interventions — of which Methotrexate is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT00783510 reports 20 study locations spanning 15 distinct geographic areas — top geographies include Illinois, New York, Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT00783510 about?
NCT00783510 is a clinical study titled "Juvenile Idiopathic Arthritis (JIA) Registry". This is a global registry, to evaluate the long-term safety of Humira® in patients with moderate to severe polyarticular Juvenile Idiopathic Arthritis (JIA), that are treated as recommended in the Humira® product label. Patients treated with MTX will be considered a reference group. Patients will be...
What is the current status of trial NCT00783510?
This trial is currently completed. The enrollment target is 849 participants. The study started on 2008-07-11. Estimated completion is 2024-02-01.
What conditions does trial NCT00783510 study?
This clinical trial studies the following conditions: Juvenile Idiopathic Arthritis, JIA. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT00783510?
The interventions under investigation include: Methotrexate (DRUG), adalimumab (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT00783510?
This trial is sponsored by AbbVie, which has 603 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT00783510 being conducted?
This trial has 20 study locations across Arizona, Arkansas, California, District of Columbia, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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