Actively Recruiting

Age: 2Years - 99Years
All Genders
Healthy Volunteers
ID01422694

Studies on the Natural History and Pathogenesis of Spondyloarthritis

Led by National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) · Updated on 2026-06-05

2000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying spondyloarthritis (SpA), a group of bone and joint disorders that cause pain and stiffness, and can lead to abnormal bone growth affecting joints and the spine. The study aims to understand which people with SpA or their relatives are more likely to develop severe forms of the disease by identifying symptoms and medical tests that predict disease progression. This includes both children and adults with SpA and healthy relatives. Participants with SpA will undergo physical exams, medical history reviews, joint movement studies, blood and urine tests, questionnaires on pain and quality of life, and imaging studies such as MRI and X-rays. Some may provide skin tissue, bone marrow, or stool samples for research, and genetic testing may be performed. Healthy relatives will give blood and cheek cell samples. No treatments are provided during the study. Participants will be followed over time with clinical assessments, imaging, laboratory tests, and questionnaires to measure disease activity and function. Researchers will track progression from SpA to more severe forms like axial SpA and ankylosing spondylitis over up to 10 years. The study collects detailed data to improve understanding of disease causes and progression, helping identify patients for future treatment studies.

CONDITIONS

Brief Title

Natural History and Development of Spondyloarthritis

Who Can Participate

Age: 2Years - 99Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Subjects with known or suspected spondyloarthritis (SpA)
  • Family members of individuals with known or suspected SpA
  • Healthy volunteers aged 6 years or older who are not pregnant
  • Minor healthy volunteers must be able to complete imaging procedures without sedation
  • Pregnant people with SpA may enroll but will not undergo MRI, skin biopsy, or bone marrow aspiration
  • Participants must provide informed consent and be able to attend follow-up visits
Not Eligible

You will not qualify if you...

  • Inability to provide informed consent or lack of parent/guardian consent for minors
  • Presence of medical conditions that could confuse study results
  • Inability or unwillingness to comply with follow-up visit schedule
  • Children under 2 years old
  • Healthy volunteers who are pregnant

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Diagnostic Evaluation

Duration - Ongoing throughout study participation

Participants undergo history, physical examination, imaging studies including MRI and X-rays, and laboratory evaluations to assess spondyloarthritis and related manifestations.

Initial baseline visit and periodic follow-up visits for assessments

Long-term Monitoring

Duration - Up to 10 years

Participants are followed over time to track disease progression and changes in signs, symptoms, imaging, and biomarkers.

Periodic visits over the course of the study for ongoing evaluation

Trial Site Locations

Total: 1 location

1

National Institutes of Health Clinical Center

Bethesda, Maryland, United States, 20892

Actively Recruiting

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Research Team

S

Sahar Lotfi-Emran, M.D.

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

3

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