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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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JPRN |
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Last refreshed on:
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17 October 2023 |
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Main ID: |
JPRN-UMIN000007679 |
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Date of registration:
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09/04/2012 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Randomized comparative study on efficacy and safety of tacrolimus, prednisolone or placebo in ocular myasthenia gravis patients
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Scientific title:
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Randomized comparative study on efficacy and safety of tacrolimus, prednisolone or placebo in ocular myasthenia gravis patients - Efficacy and safety of tacrolimus in ocular myasthenia gravis |
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Date of first enrolment:
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2012/04/01 |
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Target sample size:
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60 |
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Recruitment status: |
Recruiting |
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URL:
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https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000009056 |
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Study type:
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Interventional |
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Study design:
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Parallel Randomized
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Phase:
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Not selected
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Countries of recruitment
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Japan
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Contacts
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Name:
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Akiyuki Uzawa |
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Address:
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1-8-1 Inohana, Chuo-ku, Chiba
Japan |
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Telephone:
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Email:
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Affiliation:
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Chiba University Graduate School of Medicine Department of Neurology |
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Name:
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Address:
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1-8-1 Inohana, Chuo-ku, Chiba
Japan |
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Telephone:
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Email:
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Affiliation:
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Chiba University Graduate School of Medicine Department of Neurology |
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Key inclusion & exclusion criteria
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Inclusion criteria:
Exclusion criteria: Patients disqualified by doctor in attendance with any reason
Age minimum:
20years-old
Age maximum:
Not applicable
Gender:
Male and Female
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Health Condition(s) or Problem(s) studied
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Myasthenia gravis
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Intervention(s)
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Administration of tacrolimus 3 mg/day
Administration of prednisolone 5 mg/day
anticholinesterases
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Primary Outcome(s)
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Total QMG scores of the ocular symptomes after 4 months
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Source(s) of Monetary Support
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Chiba University
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Ethics review
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Status: YES
Approval date:
Contact:
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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