Seattle Children's Hospital
Seattle, Washington, 98105, United States
Location status: Recruiting
NCT Number: NCT04725422
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.
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All sexes
Observational
Seattle, Washington, 98105, United States
Location status: Recruiting
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs
second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs
Other names: Azulfidine
second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs
Other names: areva
second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs
Other names: Aredia
second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs
second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs
Other names: enbrel
second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs
Other names: humira
second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs
Other names: cimzia
second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs
Other names: remicade, inflectra
second-line treatment for children with CNO/CRMO after failure to respond to NSAIDs
Other names: simponi
first-line treatment
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)
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
Time frame: 5 years
Serious adverse events including infections that require IV antibiotics, malignancy, hematological, hepatic, dermatological side effects will be reported
Contact information is provided by the study sponsor or research team.
Seattle Children's Hospital
Other
CHronic Nonbacterial Osteomyelitis International Registry (CHOIR)
Acronym: CHOIR
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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