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NCT Number: NCT04725422

CHronic Nonbacterial Osteomyelitis International Registry

The objective of the study is to establish a prospective disease registry for chronic recurrent multifocal osteomyelitis (CRMO)/chronic nonbacterial osteomyelitis (CNO) in order to investigate the natural history of the disease and the responses of patients to different clinical managements over 10 years.

Recruiting

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Key information

Age range

Up to 21 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Seattle Children's Hospital

Seattle, Washington, 98105, United States

Location status: Recruiting

Location contact

Joshua Scheck, BS

CONTACT

[email protected]

206-987-2000

About this study

Chronic nonbacterial osteomyelitis (CNO) is an autoinflammatory bone disease that mainly affects children and adolescents. Clinical presentations range from mild and sometimes limited unifocal disease to severe, chronically active or recurrent inflammation of multiple bones. The latter is referred to as chronic recurrent multifocal osteomyelitis (CRMO). Here we will use the term "CNO" to refer to the entire spectrum of this disease. CNO can be complicated by vertebral compression fractures, kyphosis, and leg length discrepancy when it is not recognized early or treated adequately. The diagnosis of CNO is made by excluding alternatives in the differential diagnosis including malignancy (leukemia, lymphoma, and primary or metastatic bone tumors), Langerhans cell histiocytosis, and infection. Clinical assessment in conjunction with serum inflammatory parameters and imaging studies, particularly magnetic resonance imaging (MRI), are crucial for the diagnosis and monitoring of disease activity of CNO1.

Because of significant variation in clinical treatment practices among pediatric rheumatologists, standardized treatment regimens (consensus treatment plans, CTPs) have been developed within the Childhood Arthritis and Rheumatology Research Alliance (CARRA), a North American organization comprised of pediatric rheumatologists and researchers, for CNO patients with an NSAID-refractory course and/or with active spinal lesions2. These CTPs provide an opportunity for pediatric rheumatologists to conduct comparative effectiveness research on CNO through prospective data collection. CRMO/CNO workgroup is comprised of pediatric rheumatologists from North America as well as international colleagues who are interested in collaborating in CNO research. Furthermore, risk factors of severe disease have been described by Wipff et al. based on a large retrospective cohort study3. Their results may be validated by an independent prospective cohort study. To date, there has been only one prospective study on CNO since its first description in 19724. Therefore, we propose to establish this international registry of patients with CNO to accomplish above goals. Long-term outcomes of CNO remains unknown due to the lack of prospective study. It has been estimated that at least 50% of CNO patients continue to need medications for CNO during adulthood. Our study will collect the clinical data and provide valuable data to characterize the long-term outcomes.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • - Age at enrollment is equal to or younger than 21 years of age
  • Presence of bone edema on STIR or T2 fat saturation sequence on MRI within 12 weeks of enrollment
  • Whole body imaging evaluation (either WB MRI or bone scintigraphy)
  • Bone biopsy to exclude infection or malignancy unless bone lesions follow typical distribution or there is IBD, psoriasis, or palmar plantar pustulosis

Exclusion criteria

  • - History of or current malignancy
  • Current infectious osteomyelitis
  • Contraindication to the selected treatment agent

Treatment and study plan

methotrexate

Drug

second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs

Sulfasalazine

Drug

second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs

Other names: Azulfidine

leflunomide

Drug

second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs

Other names: areva

Pamidronate

Drug

second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs

Other names: Aredia

Zoledronic acid

Drug

second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs

etanercept

Drug

second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs

Other names: enbrel

Adalimumab

Drug

second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs

Other names: humira

Certolizumab

Drug

second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs

Other names: cimzia

Infliximab

Drug

second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs

Other names: remicade, inflectra

Golimumab

Drug

second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs

Other names: simponi

NSAID

Drug

first-line treatment

Primary outcomes

  1. The change of CNO disease activity score

    Time frame: 3-6 months

    Disease activity score is calculated as the sum of number of clinical lesion count, patient global assessment (0-10), physician global assessment (0-10)

Secondary outcomes

  1. Total number of CNO lesions on MRI

    Time frame: 3-6 months

    The total number of CNO lesions from MRI as previously described (Zhao, et al. J Rheum 2019) will be used to monitor response in a subset

  2. Safety monitoring

    Time frame: 5 years

    Serious adverse events including infections that require IV antibiotics, malignancy, hematological, hepatic, dermatological side effects will be reported

Study contacts

Contact information is provided by the study sponsor or research team.

Yongdong (Dan) Zhao, MD, PhD

CONTACT

[email protected]

206-987-2000

Sponsors and collaborators

Lead sponsor

Seattle Children's Hospital

Other

Collaborators

  • Alder Hey Children's NHS Foundation Trust
  • Ann & Robert H Lurie Children's Hospital of Chicago
  • Bambino Gesù Children's Hospital, Rome, Italy
  • Boston Children's Hospital, Boston, MA, USA
  • Hacettepe University
  • Hospital for Special Surgery, New York
  • Joseph M Sanzari Children's Hospital, Hackensack University Medical Center, Hackensack, NJ, USA
  • Mansoura University
  • Meyer Children's Hospital, Florence, Italy
  • Palacky University Olomouc Institute of Molecular and Translational Medicine, Olomouc, Czechia
  • Riley Children's Hospital, Indianapolis, IN, USA
  • Royal Children's Hospital
  • University of British Columbia, Vancouver, BC, Canada
  • University of Calgary
  • University of Iowa Carver College of Medicine, Iowa City, IA, USA
  • University of North Carolina, Chapel Hill, NC, USA
  • University of Utah, Salt Lake City, UT, USA

Registry information

Official study title

CHronic Nonbacterial Osteomyelitis International Registry (CHOIR)

Acronym: CHOIR

Important dates

Study start
2018
Primary completion
2028
Study completion
2050
First posted
Jan 26, 2021
Registry last updated
Jul 30, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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