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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-UMIN000007419 |
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Date of registration:
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01/04/2012 |
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Prospective Registration:
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Yes |
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Primary sponsor: |
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Public title:
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A Prospective, Randomized, Multicenter Trial of Pregabalin and Celecoxib for Lumbar Spinal Stenosis
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Scientific title:
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A Prospective, Randomized, Multicenter Trial of Pregabalin and Celecoxib for Lumbar Spinal Stenosis - A Prospective, Randomized, Multicenter Trial of Pregabalin and Celecoxib for Lumbar Spinal Stenosis |
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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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80 |
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Recruitment status: |
Pending |
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URL:
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https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000008738 |
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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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Koichiro Maeno |
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Address:
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7-5-2 Kusunoki-cyo Cyuou-ku Kobe-city Hyogo-prefecture Japan
Japan |
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Telephone:
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078-382-5985 |
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Email:
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takada-t@hokuto-hp.or.jp |
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Affiliation:
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Kobe university Graduate School of Medicine Department of Orthopedic Surgery |
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Name:
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Koichiro Maeno |
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Address:
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7-5-2 Kusunoki-cyo Cyuou-ku Kobe-city Hyogo-prefecture Japan
Japan |
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Telephone:
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078-382-5985 |
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Email:
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takada-t@hokuto-hp.or.jp |
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Affiliation:
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Kobe university Graduate School of Medicine Department of Orthopedic Surgery |
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Key inclusion & exclusion criteria
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Inclusion criteria:
Exclusion criteria: Arteriosclerosis obliterans Diabetic neuropathy Anterior tibial muscle MMT 3 and below Ineffectiveness of epidural block over 3 times in a month Vesicorectal disturbance Heart failure Herniated disc disase
Age minimum:
50years-old
Age maximum:
90years-old
Gender:
Male and Female
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Health Condition(s) or Problem(s) studied
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Lumbar Spinal Stenosis
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Intervention(s)
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Celecoxib
Pregabalin
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Primary Outcome(s)
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The recovery of pain and ADL four weeks after the administration
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Secondary Outcome(s)
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The recovory of NRS, ODI, SF-36 score four weeks after the administration
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Source(s) of Monetary Support
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Department of Orthopedic Surgery Kobe University Graduate School of Medicine
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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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