Magnesium Sulfate in Thrombotic Thrombocytopenic Purpura in Intensive Care (MAGMAT)
Primary Purpose
Thrombotic Thrombocytopenic Purpura
Status
Unknown status
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Sulfate, Magnesium
Placebo - Concentrate
Sponsored by
About this trial
This is an interventional treatment trial for Thrombotic Thrombocytopenic Purpura focused on measuring Thrombotic Thrombocytopenic Purpura, Intensive care
Eligibility Criteria
Inclusion Criteria:
- Age > or = 18 years
- Health insurance
- Signed inform consent by patient or relatives
Exclusion Criteria:
- Pregnancy
- No health insurance
Sites / Locations
- Saint Louis hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Experimental
Arm Label
Placebo
Magnesium Sulfate
Arm Description
Glucose serum (3 ampoules)
20/5000 magnesium sulfate (4 ampoules, 1,5g each)
Outcomes
Primary Outcome Measures
Time to normalization of the platelet count
Normalization of the platelet is defined as a platelet count that reaches at least 150,000 per cubic millimeter for 48 consecutive hours
Secondary Outcome Measures
Duration and volume of plasma exchanges
platelet count
proportion of subjects with refractory TTP
absence of platelet count doubling after 4 days of standard treatment
Proportion of subjects with an exacerbation of TTP
recurrence during the 30 days after the last daily plasma exchange
Proportion of subjects with a relapse of TTP
recurrence occurring more than 30 days after the last daily plasma exchange
Cardiac trouble frequency
Cerebral trouble frequency
Acute kidney injury
Kidney Disease: Improving Global Outcomes (KDIGO) score > or = 1
Time to normalization of hemolysis marker levels
Lactate dehydrogenase (LDH), haptoglobin, bilirubinemia, hemoglobin
Hospital length of stay
Hospital mortality
90 days after randomization
ICU length of stay
ICU mortality
Adverse events related to the use of magnesium sulfate
Full Information
NCT ID
NCT03237819
First Posted
June 13, 2017
Last Updated
October 28, 2021
Sponsor
Assistance Publique - Hôpitaux de Paris
1. Study Identification
Unique Protocol Identification Number
NCT03237819
Brief Title
Magnesium Sulfate in Thrombotic Thrombocytopenic Purpura in Intensive Care
Acronym
MAGMAT
Official Title
Interest of Magnesium Sulfate in Thrombotic Thrombocytopenic Purpura in Intensive Care: Multicentric Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
June 2021
Overall Recruitment Status
Unknown status
Study Start Date
May 27, 2018 (Actual)
Primary Completion Date
December 1, 2021 (Anticipated)
Study Completion Date
December 1, 2021 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
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
Thrombotic Thrombocytopenic Purpura (TTP) is a potentially life-threatening thrombotic microangiopathy caused by a severe deficiency of ADAMTS13 (a disintegrin and metalloproteinase with a thrombospondin type 1 motif member 13). Decreased ADAMTS13 activity leads to an accumulation of ultralarge von Willebrand factor (vWF) multimers which induce aggregation of platelets and microthrombi. These microthrombi may involve the brain, heart, kidneys and lead to life-threatening organ failures.
In experimental models, magnesium sulfate increases cleavage of newly released vWF by ADAMTS13, decreases the endothelial secretion of ultralarge vWF and inhibits the interaction of vWF with platelets. In another thrombotic microangiopathy, magnesium sulfate has been shown to reduce the risk of seizures in women with severe pre-eclampsia. In analogy with its evidence-based therapeutic application in pre-eclampsia and based on a strong rationale for magnesium supplementation in TTP, we propose a phase 3, double blind, placebo controlled, and randomized study to evaluate the efficacy of magnesium sulfate in more rapidly restoring normal platelet counts as measure of prevention of further microvascular thrombosis in patients with Thrombotic Thrombocytopenic Purpura.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Thrombotic Thrombocytopenic Purpura
Keywords
Thrombotic Thrombocytopenic Purpura, Intensive care
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
multicentre double-blind randomized clinical trial
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
For each day of treatment, 4 ampoules of 10 ml will be distributed to the patient's nurse (4 ampoules of 1.5g of magnesium sulphate or 3 ampoules of 5% glucose as placebo).
The bulbs will be labeled identically so that the blind can be maintained Moreover, in order to preserve the blind, the dosage of magnesemia should not be performed outside of a necessity judged by the clinician in charge of the patient
Allocation
Randomized
Enrollment
74 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Glucose serum (3 ampoules)
Arm Title
Magnesium Sulfate
Arm Type
Experimental
Arm Description
20/5000 magnesium sulfate (4 ampoules, 1,5g each)
Intervention Type
Drug
Intervention Name(s)
Sulfate, Magnesium
Intervention Description
Magnesium sulphate will be administered at a dose of 6g over 20 min intravenously followed by a continuous infusion of 6g / 24h for 3 days.
For each day of treatment, 4 ampoules of 10 ml will be distributed to the nurse in charge of the patient (4 ampoules of 1,5g of magnesium sulfate)
Intervention Type
Drug
Intervention Name(s)
Placebo - Concentrate
Intervention Description
For each day of treatment, 4 ampoules of 10 ml will be distributed to the nurse in charge of the patient (4 ampoules of glucose 5% as placebo)
Primary Outcome Measure Information:
Title
Time to normalization of the platelet count
Description
Normalization of the platelet is defined as a platelet count that reaches at least 150,000 per cubic millimeter for 48 consecutive hours
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Duration and volume of plasma exchanges
Time Frame
30 days
Title
platelet count
Time Frame
5 days
Title
proportion of subjects with refractory TTP
Description
absence of platelet count doubling after 4 days of standard treatment
Time Frame
5 days
Title
Proportion of subjects with an exacerbation of TTP
Description
recurrence during the 30 days after the last daily plasma exchange
Time Frame
30 days
Title
Proportion of subjects with a relapse of TTP
Description
recurrence occurring more than 30 days after the last daily plasma exchange
Time Frame
3 months
Title
Cardiac trouble frequency
Time Frame
day 30
Title
Cerebral trouble frequency
Time Frame
day 30
Title
Acute kidney injury
Description
Kidney Disease: Improving Global Outcomes (KDIGO) score > or = 1
Time Frame
day 30
Title
Time to normalization of hemolysis marker levels
Description
Lactate dehydrogenase (LDH), haptoglobin, bilirubinemia, hemoglobin
Time Frame
day 30
Title
Hospital length of stay
Time Frame
day 90
Title
Hospital mortality
Description
90 days after randomization
Time Frame
day 90
Title
ICU length of stay
Time Frame
day 90
Title
ICU mortality
Time Frame
day 90
Title
Adverse events related to the use of magnesium sulfate
Time Frame
day 7
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age > or = 18 years
Health insurance
Signed inform consent by patient or relatives
Exclusion Criteria:
Pregnancy
No health insurance
Facility Information:
Facility Name
Saint Louis hospital
City
Paris
ZIP/Postal Code
75010
Country
France
12. IPD Sharing Statement
Plan to Share IPD
Undecided
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Magnesium Sulfate in Thrombotic Thrombocytopenic Purpura in Intensive Care
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