Corticosteroid Effects on Asymptomatic Gadolinium-enhancing Lesions in Multiple Sclerosis
Primary Purpose
Multiple Sclerosis, Relapsing-Remitting, Magnetic Resonance Imaging, Methylprednisolone
Status
Unknown status
Phase
Phase 2
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
Methylprednisolone succinate
Normal saline
Sponsored by
About this trial
This is an interventional treatment trial for Multiple Sclerosis, Relapsing-Remitting focused on measuring Multiple sclerosis, Methylprednisolone Pulse therapy, Asymptomatic enhancing lesions, Chronic black hole
Eligibility Criteria
Inclusion Criteria:
- All patients with a diagnosis of RR-MS
- with a baseline MRI scan with at least one asymptomatic CEL on contrast-enhanced T1-weighted images
Exclusion Criteria:
- Pulse therapy 3 months ago,
- More than 6 months ago slowly progressive disease
- Systemic infections, including fungal infection
- Uncontrolled hypertension
- With known hypersensitivity to the steroid preparation
Sites / Locations
- Mazandaran University of medical sciences
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
The intervention group
The control group
Arm Description
The intervention group will receive 1 gram of methylprednisolone succinate within 500 ccs of normal saline within 5 hours.
The control group will receive 500 g of normal saline without methylprednisolone succinate.
Outcomes
Primary Outcome Measures
Number of black hole
NeBH (to non-enhancing black hole) was defined as an area of unequivocal low signal intensity compared with normal-appearing white matter that did not show contrast uptake and was concordant with a hyperintense lesion seen on T2-weighted imaging.They have also been defined as T1-hypointensities persisting for more than 6 months after their appearance
Expanded disability status scale
The EDSS quantifies disability in eight functional systems: pyramidal, cerebellar, brainstem, sensory, bowel and bladder, visual, cerebral, and other. It ranges from 1.0 to 4.5 for people affected with MS who are fully ambulatory, and from 5.0 to 9.5 for people with MS with impaired ambulation. The maximum grade, 10.0, represents death due to MS
Secondary Outcome Measures
Full Information
NCT ID
NCT04979650
First Posted
July 2, 2021
Last Updated
July 30, 2021
Sponsor
Mazandaran University of Medical Sciences
1. Study Identification
Unique Protocol Identification Number
NCT04979650
Brief Title
Corticosteroid Effects on Asymptomatic Gadolinium-enhancing Lesions in Multiple Sclerosis
Official Title
Corticosteroid Pulse Therapy Effects on MRI Asymptomatic Gadolinium-enhancing Lesions Conversion to a Non-enhancing Black Hole With or Without Treatment in MS Clinic of Booalisina Hospital Sari 2021-2023
Study Type
Interventional
2. Study Status
Record Verification Date
July 2021
Overall Recruitment Status
Unknown status
Study Start Date
May 22, 2021 (Actual)
Primary Completion Date
May 22, 2023 (Anticipated)
Study Completion Date
October 23, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Mazandaran University of Medical Sciences
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
to determine the rate of asymptomatic gadolinium-enhancing lesions conversion to the non-enhancing black hole (neBHs) with or without corticosteroid pulse therapy in patients with RRMS, and to analyze if treatment of asymptomatic gadolinium enhancement lesions has any effect on the expanded disability status scale. The study is performed in the MS clinic of Bu Ali Sina Hospital in Sari and Mazandaran University of Medical Sciences. 104 recurrent MS patients are admitted based on the admission criteria. They are divided into two groups of intervention and control based on a simple randomization block. The intervention group received 1 gram of methylprednisolone in 500 ccs of normal saline for 5 days and the control group received only 500 ccs of serum. After 6 months, a new MRI is taken from the patients and the possibility of asymptomatic active plaque conversion with or without intervention is compared in the two groups, as well as the amount of EDSS in the two groups. They do not know whether the patient is in the control group or the intervention.
Detailed Description
Investigators perform a study on 104 consecutive patients with a diagnosis of RR-MS. Participants will be selected for the study if they meet all of the following inclusion criteria: (1) a baseline MRI scan with at least one CEL on contrast-enhanced T1-weighted images (performed either at the time of the diagnosis or during the routine MRI monitoring of the disease) and (2) a follow-up MRI scan performed at least 6 months later in the same hospital site. Participants were then divided into two groups by block randomization (the Block size will be 4): (1) participants with asymptomatic CELs, treated with a single cycle of high-dose IVMP after baseline MRI (group A) and (2) participants with asymptomatic CELs for clinical relapse and, therefore, not exposed to IVMP after baseline MRI (group B).
Microsoft Excel software will be used for block randomization with a group of 4.
Number the participants from 1 to 102.
In a group of 2, the possible combinations of blocks are:(A=Group1 and B=Group2)
1. ABBA 2. ABAB 3. BBAA 4. ABAB 5. BAAB 6. BABA
To determine the sample size for this study we used the result of Maria Di Gregorio and et al.
This study will be double-blind patients and radiologist clinicians unaware of types of interventions.
MRI examinations were performed with a 1.5 T magnet (General Electric Medical Systems, Milwaukee, WI, USA) with a standard head coil. The MRI protocol used in our Neuroradiology Section included the following sequences: (1) a T2-weighted-fluid-attenuated inversion recovery (FLAIR) sequence with an inversion time (TI) of 2400 ms, an echo time (TE) of 120 ms, and a repetition time (TR) of 8000 ms; (2) a T2-weighted fast spin-echo (FSE) sequence with a TE of 90 ms and a TR of 6600 ms; and (3) a spin-echo (SE) sequence for T1-weighted images with a TR of 500 ms and a TE of 20 ms Post-contrast images were obtained with a scan delay of 5 min after the injection of gadoterate (Dotarem, Guerbet group, Roissy, France) at 0.2 mmol/kg. 3-mm thick contiguous slices were obtained.
In the baseline MRI, the following characteristics of CELs were recorded: (1) number; (2) maximum diameter (≤ or > 5 mm); (3) pattern of enhancement (homogeneous or ring enhancement); (4) hypointensity as compared to normal-appearing surrounding white matter in baseline T1-weighted images acute black hole (aBH); and (5) the fact of being symptomatic, as established by an experienced neurologist (MDG) on the basis of CELs' localization and clinical characteristics of the concomitant relapse. The follow-up MRI was performed with the same 1.5 T magnet and using the same MRI protocol. At the follow-up MRI, the presence of persistent black holes (pBHs) was recorded. Specifically, pBHs were defined as non-enhancing T1 lesions hypointense with respect to the surrounding normal-appearing white matter and concordant with hyperintense T2 lesions [10]. Three investigators (MDG, AP, and GR) in agreement with a senior experienced neuro-radiologist (PF) revised baseline CELs and follow-up pBHs' characteristics. The three investigators and the neuroradiologist were blinded to the exposure of the patients to IVMP treatment
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Multiple Sclerosis, Relapsing-Remitting, Magnetic Resonance Imaging, Methylprednisolone
Keywords
Multiple sclerosis, Methylprednisolone Pulse therapy, Asymptomatic enhancing lesions, Chronic black hole
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
104 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
The intervention group
Arm Type
Active Comparator
Arm Description
The intervention group will receive 1 gram of methylprednisolone succinate within 500 ccs of normal saline within 5 hours.
Arm Title
The control group
Arm Type
Placebo Comparator
Arm Description
The control group will receive 500 g of normal saline without methylprednisolone succinate.
Intervention Type
Drug
Intervention Name(s)
Methylprednisolone succinate
Other Intervention Name(s)
Active
Intervention Description
1 gram of methylprednisolone succinate within 500 ccs of normal saline
Intervention Type
Drug
Intervention Name(s)
Normal saline
Other Intervention Name(s)
Placebo
Intervention Description
500 g of normal saline without methylprednisolone succinate
Primary Outcome Measure Information:
Title
Number of black hole
Description
NeBH (to non-enhancing black hole) was defined as an area of unequivocal low signal intensity compared with normal-appearing white matter that did not show contrast uptake and was concordant with a hyperintense lesion seen on T2-weighted imaging.They have also been defined as T1-hypointensities persisting for more than 6 months after their appearance
Time Frame
After 6 months
Title
Expanded disability status scale
Description
The EDSS quantifies disability in eight functional systems: pyramidal, cerebellar, brainstem, sensory, bowel and bladder, visual, cerebral, and other. It ranges from 1.0 to 4.5 for people affected with MS who are fully ambulatory, and from 5.0 to 9.5 for people with MS with impaired ambulation. The maximum grade, 10.0, represents death due to MS
Time Frame
After 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All patients with a diagnosis of RR-MS
with a baseline MRI scan with at least one asymptomatic CEL on contrast-enhanced T1-weighted images
Exclusion Criteria:
Pulse therapy 3 months ago,
More than 6 months ago slowly progressive disease
Systemic infections, including fungal infection
Uncontrolled hypertension
With known hypersensitivity to the steroid preparation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Seyed Mohammad Baghbanian, Dr.
Organizational Affiliation
Mazandaran University of Medical Sciences
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mazandaran University of medical sciences
City
Sari
State/Province
Mazandaran
ZIP/Postal Code
4815838477
Country
Iran, Islamic Republic of
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing Plan Description
All data is potentially shareable after unidentified individuals.
IPD Sharing Time Frame
The access period starts 6 months after the results are published.
IPD Sharing Access Criteria
It will be available only to researchers working in academic and scientific institutions.
Learn more about this trial
Corticosteroid Effects on Asymptomatic Gadolinium-enhancing Lesions in Multiple Sclerosis
We'll reach out to this number within 24 hrs