Pediatric NMOSD Observational Study

Completed

• Conditions: Neuromyelitis Optica; NMO Spectrum Disorder

• Registration Number: NCT03766347
• Lead Sponsor: Mayo Clinic

Brief Summary

This study is being done to develop a database of pediatric patients in order to study the cause, early detection and best treatment for neuromyelitis optica spectrum disorder (NMOSD) in pediatric patients.

Detailed Description

This study is being done to collect information on the natural history of NMOSD in pediatric AQP4-IgG seropositive patients. A major restriction in performing drug studies in pediatric patients with NMOSD is limited information on the course of the disease in these patients. Collecting clinical information over the course of a 1 year observational study would inform on the natural history of the disease in these patients. A repository of pediatric patients with rare diseases can increase knowledge on the natural history of the specific disease, assist in identifying appropriate patients fulfilling specified criteria for drug studies and potentially serve as a control group.

Timepoints: Baseline, 3mo, 6mo, 9mo, 12mo (+/- 1 mo for each time point).

Baseline data:

* Demographics \[age/sex/ethnicity\],

* Clinical presentation information including date of initial diagnosis,

* Clinical phenotype

* Immunotherapy used current and past,

* Family history of autoimmune diseases,

* Serological data results

* Radiologic data as available

Self-Report Assessments will be:

* Current impairment, as measured by the expanded disability status scale (EDSS) score self-reported using Ratzker (1997) EDSS Self Report form,

* Quality of life as measured by the EQ-5D and Varni's (1998) PedsQL over the phone/mail/email.

At follow-up visits 3mo, 6mo, 9mo, 12mo (+/- 1 mo for each time point):

* Attacks/relapses

* Any hospitalizations

* Confirm medications and update records if changes

Self-Report Assessments at follow-up will be:

* Current impairment, as measured by the EDSS score self-reported using Ratzker (1997) EDSS Self Report form,

* Quality of life as measured by the EQ-5D and PedsQL over the phone/mail/email.

Study Timeline

• Study Start: 2018-02-01
• Study First Submitted: 2018-12-04
• Study First Submitted QC: 2018-12-04
• Study First Posted: 2018-12-06
• Status Verified: 2024-04
• Primary Completion: 2024-04-03
• Study Completion: 2024-04-03
• Last Update Submitted: 2024-04-08
• Last Update Posted: 2024-04-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 100

Inclusion Criteria

• AQP4 positive
• Ability to give informed consent by patient or caregiver

Exclusion Criteria

• Inability to complete required forms via phone, mail, or email.

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Time to relapse	One year.	Relapse events of NMOSD defined by clinical worsening of neurological symptoms and treatment.

Trial Locations

Locations (1)

Mayo Clinic; 🇺🇸 Rochester, Minnesota, United States