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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-UMIN000015852 |
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Date of registration:
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05/12/2014 |
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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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Bone augmentation by octacalcium and collagen composite
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Scientific title:
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Bone augmentation by octacalcium and collagen composite - Bone augmentation by OCP/Collagen |
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Date of first enrolment:
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2014/12/05 |
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Target sample size:
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11 |
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Recruitment status: |
Complete: follow-up complete |
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URL:
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https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000018447 |
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Study type:
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Interventional |
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Study design:
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Single arm Non-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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Tadashi Kawai |
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Address:
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1-1, Seiryo-machi, Aoba-ku, Sendai, MIyagi
Japan |
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Telephone:
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022-717-8350 |
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Email:
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ta-shi@dent.tohoku.ac.jp |
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Affiliation:
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Tohoku University Hospital Oral and Maxillofacial Surgery |
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Name:
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Tadashi Kawai |
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Address:
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1-1, Seiryo-machi, Aoba-ku, Sendai, MIyagi
Japan |
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Telephone:
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022-717-8350 |
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Email:
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ta-shi@dent.tohoku.ac.jp |
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Affiliation:
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Tohoku University Hospital Oral and Maxillofacial Surgery |
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Key inclusion & exclusion criteria
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Inclusion criteria:
Exclusion criteria: Patient suffering severe hepatopathy, renal disorders, and heart disease who would affect safety evaluation of this trial Patient who has an allergy drug Patient who is pregnant, possibly pregnant, nursing or considering pregnancy Patient who participated other clinical trial program within 3 months prior to the study entry Others, patient who is unfit for the study as determined by the principal investigator or sub-investigators
Age minimum:
20years-old
Age maximum:
65years-old
Gender:
Male and Female
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Health Condition(s) or Problem(s) studied
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Missing tooth
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Intervention(s)
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Implantation of OCP/Collagen as a bone sbstitute material with sinus floor augmentation.
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Primary Outcome(s)
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Histological analysis, Radiographycal analysis, Safety assessment by clinical examination and adverse event
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Source(s) of Monetary Support
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Tohoku 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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