CHronic Nonbacterial Osteomyelitis International Registry

NCT04725422 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 2000

Last updated 2024-07-30

No results posted yet for this study

Summary

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.

Conditions

  • Chronic Nonbacterial Osteomyelitis
  • Chronic Recurrent Multifocal Osteomyelitis

Interventions

DRUG

Methotrexate

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

DRUG

Sulfasalazine

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

DRUG

Leflunomide

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

DRUG

Pamidronate

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

DRUG

Zoledronic acid

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

DRUG

Etanercept

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

DRUG

Adalimumab

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

DRUG

Certolizumab

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

DRUG

Infliximab

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

DRUG

Golimumab

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

DRUG

NSAID

first-line treatment

Sponsors & Collaborators

  • Boston Children's Hospital, Boston, MA, USA

    collaborator OTHER
  • Hospital for Special Surgery, New York

    collaborator OTHER
  • Joseph M Sanzari Children's Hospital, Hackensack University Medical Center, Hackensack, NJ, USA

    collaborator UNKNOWN
  • Riley Children's Hospital, Indianapolis, IN, USA

    collaborator UNKNOWN
  • University of North Carolina, Chapel Hill, NC, USA

    collaborator UNKNOWN
  • Royal Children's Hospital

    collaborator OTHER
  • Hacettepe University, Ankara, Turkey

    collaborator UNKNOWN
  • Bambino Gesù Children's Hospital, Rome, Italy

    collaborator UNKNOWN
  • University of British Columbia, Vancouver, BC, Canada

    collaborator UNKNOWN
  • Meyer Children's Hospital, Florence, Italy

    collaborator UNKNOWN
  • Mansoura University

    collaborator OTHER
  • University of Utah, Salt Lake City, UT, USA

    collaborator UNKNOWN
  • University of Iowa Carver College of Medicine, Iowa City, IA, USA

    collaborator UNKNOWN
  • Ann & Robert Lurie Children's Hospital of Chicago, Chicago, IL, USA

    collaborator UNKNOWN
  • Palacky University Olomouc Institute of Molecular and Translational Medicine, Olomouc, Czechia

    collaborator UNKNOWN
  • Alder Hey Children's NHS Foundation Trust Hospital, Liverpool, UK

    collaborator UNKNOWN
  • University of Calgary, Calgary, Alberta, Canada

    collaborator UNKNOWN
  • Seattle Children's Hospital

    lead OTHER

Eligibility

Max Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-08-01
Primary Completion
2028-08-31
Completion
2050-08-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04725422 on ClinicalTrials.gov