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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01623076
Other study ID # STU 022012-084
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date June 2012
Est. completion date June 2025

Study information

Verified date September 2023
Source University of Texas Southwestern Medical Center
Contact Jan Cameron-Watts, RN
Phone 214-645-0555
Email jan.cameronwatts@utsouthwestern.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study seeks to determine the biologic causes of inflammation in patients with Transverse Myelitis (TM) Neuromyelitis Optica Spectrum Disorder (NMOSD) and related conditions. While patients will be treated according to decisions with their treating physician, this study will collect data and samples from patients prospectively to gain a better understanding of the disease. We are seeking to understand why some patients respond to medications, while others do not. We also seek to understand what happens biologically, preceding relapses. Gathering these data and samples will allow researchers to identify new ways of diagnosing and treating these diseases. Data and samples will be shared with researchers around the world to support collaborative efforts to treat these conditions.


Description:

This study seeks to determine the biologic causes of inflammation in patients with Neuromyelitis Optica (NMO), Transverse Myelitis (TM), optic neuritis (ON), related conditions and healthy controls. While patients will be treated according to decisions with their treating physician, this study will collect data and samples from patients prospectively to gain a better understanding of the disease. We are seeking to understand why some patients respond to medications, while others do not. We also seek to understand what happens biologically, preceding relapses. Gathering these data and samples will allow researchers to identify new ways of diagnosing and treating these diseases. Data and samples will be shared with researchers around the world to support collaborative efforts to treat these conditions. Patients will agree to share medical records, complete questionnaires and donate samples on a timed basis.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date June 2025
Est. primary completion date June 2025
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 6 Years and older
Eligibility Inclusion Criteria: - Age 6 years or greater - Male or Female - Patient or Parent (in the case of a minor) able to give informed consent - For patients 10 to 17, patient able to assent - Patient diagnosed with NMO, NMOSD, TM or ON Exclusion Criteria: - Unable to maintain scheduled visits - Patient has known HIV or hepatitis C infection

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States The University of Texas Southwestern Medical Center Dallas Texas

Sponsors (1)

Lead Sponsor Collaborator
University of Texas Southwestern Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Measure change in standard clinical assessments over time Standard clinical assessments include: relapse information, level of disability based on EDSS score, high and low contract visual acuity, ambulation index, optical coherence tomography, and MRI, and neurologic/physical exam Every study visit
Secondary Measure change in cognition measures over time Cognition measures include the SDMT, JLO, and PASAT Every study visit
Secondary Measure change in self-reported quality of life surveys Surveys include MSNQ, MSQOL-54, QIDS, BDI-II, FSS, ESS, MFIS, BPI, and Neuro-QoL Every study visit
Secondary B cell population changes Measure B cell subtypes and changes over time Up to 5 years
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