Examining Effects of Tysabri on Cognitive Fatigue Using fMRI
NCT04565431 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 25
Last updated 2024-02-15
Summary
The purpose of this research study is to investigate the effectiveness of Tysabri on cognitive fatigue in persons with Relapsing-Remitting Multiple Sclerosis (RRMS). Cognitive fatigue is the kind of fatigue that occurs after intense mental concentration as after a session of problem solving.
Conditions
- Multiple Sclerosis, Relapsing-Remitting
Interventions
- DRUG
-
Tysabri
Participants with RRMS who are planning to begin treatment with Tysabri will be compared to a group of healthy individuals who are matched for age, gender, and education.
Sponsors & Collaborators
-
St. Barnabas Medical Center
collaborator OTHER -
Kessler Foundation
lead OTHER
Principal Investigators
-
John DeLuca, Ph.D. · Kessler Foundation
Eligibility
- Min Age
- 18 Years
- Max Age
- 64 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2021-03-19
- Primary Completion
- 2024-12-31
- Completion
- 2024-12-31
- FDA Drug
- Yes
Countries
- United States
Study Locations
More Related Trials
-
Evaluation of Early Changes Visible to the Diffusion MRI in Response to Two Years of Treatment With Tysabri in Patients With Multiple Sclerosis
NCT02904876 ·Status: TERMINATED ·Phase: PHASE4
-
A Study to Assess the Effects of MK0812 on Disease Activity in Patients With Relapsing-Remitting Multiple Sclerosis as Measured by Magnetic Resonance Imaging (MRI)(0812-003)(COMPLETED)
NCT00239655 ·Status: TERMINATED ·Phase: PHASE2
-
Validation of a Laboratory Test Measuring Natalizumab (Tysabri®) Serum Levels in MS
NCT02965170 ·Status: COMPLETED
-
The Effect of Natalizumab (Tysabri) on Sexual Dysfunction in Multiple Sclerosis
NCT01455220 ·Status: COMPLETED ·Phase: NA
-
fMRI Study of Treatment Recommendations Comparing Recently Diagnosed Multiple Sclerosis (MS) Patients to Controls
NCT00391352 ·Status: COMPLETED
-
A Longitudinal Study of Brain Atrophy in MS Patients Over 5 Years
NCT01847287 ·Status: COMPLETED
-
FOCUS Fatigue Outcome in Copaxone USers
NCT00267319 ·Status: COMPLETED ·Phase: PHASE4
-
Grey Matter Damage at the Earliest Phase of Multiple Sclerosis : a Longitudinal 7T MRI Study
NCT03659981 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Dose-finding Study for SAR442168 in Relapsing Multiple Sclerosis
NCT03889639 ·Status: COMPLETED ·Phase: PHASE2
-
Fatigue in Multiple Sclerosis: Evaluated With 3 MRI and Transcranial Magnetic Stimulation
NCT00342381 ·Status: COMPLETED ·Phase: PHASE2
-
Magnetic Resonance Imaging (MRI) to Evaluate Activity of Multiple Sclerosis (MS)
NCT00001248 ·Status: RECRUITING
-
Ireland Natalizumab (TYSABRI) Observational Program
NCT01943526 ·Status: COMPLETED
-
Evaluation of Natalizumab for thE Relief of MS Associated FatiGue
NCT00464074 ·Status: COMPLETED
-
Fatigue in MS: From Invisible to Measurable
NCT07182903 ·Status: COMPLETED
-
Study of Tysabri in Early Relapsing Remitting Multiple Sclerosis Participants
NCT04832399 ·Status: COMPLETED
-
NAPS-MS: NAtalizumab Effects on Parameters of Sleep in Patients With Multiple Sclerosis Experiencing Fatigue or Sleepiness
NCT01591551 ·Status: COMPLETED ·Phase: PHASE4
-
Efficacy and Safety of FTY720 in Patients With Relapsing Multiple Sclerosis
NCT00333138 ·Status: COMPLETED ·Phase: PHASE2
-
Tysabri Observational Program
NCT00493298 ·Status: COMPLETED
-
TMP001 in Relapsing-remitting Multiple Sclerosis
NCT02686788 ·Status: COMPLETED ·Phase: PHASE2
-
An fMRI Study of Treatment Optimization Comparing Two Disease Modifying Therapies Used to Treat Relapsing Remitting Multiple Sclerosis
NCT00398528 ·Status: TERMINATED
-
Cognitive Effects of Immunomodulatory Drugs in MS
NCT00229502 ·Status: COMPLETED
-
Longitudinal Pharmacokinetic, Pharmacodynamic, Immunological, and Biochemical
NCT01330498 ·Status: COMPLETED
-
Understanding Magnetic Resonance Imaging in Multiple Sclerosis
NCT03872583 ·Status: COMPLETED ·Phase: NA
-
Study of the Safety and Efficacy of MLN1202 in Patients in Multiple Sclerosis
NCT01199640 ·Status: COMPLETED ·Phase: PHASE2
-
Safety, Tolerability, and Effectiveness of CGP77116 in Patients With Multiple Sclerosis (MS)
NCT00001781 ·Status: COMPLETED ·Phase: PHASE2