Name: UMIN ID:
Unique ID issued by UMIN | UMIN000005079 |
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Receipt number | R000006042 |
Scientific Title | A randomized double blind, placebo-controlled trial of efficacy and safety of Kamishoyosan in patients with climacteric symptoms |
Date of disclosure of the study information | 2011/03/01 |
Last modified on | 2013/02/25 17:40:48 |
No. | Disposal | Last modified on | Item of update | |
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1 | Insert | 2011/02/14 15:17:05 | ||
2 | Update | 2011/03/11 13:27:32 | Co-sponsor Co-sponsor |
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3 | Update | 2011/03/11 13:42:28 | Co-sponsor Co-sponsor |
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4 | Update | 2013/02/06 16:40:58 | Post marketing survey by drug manufacture etc., specified by Japanese law. |
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5 | Update | 2013/02/06 16:45:38 | Recruitment status Last follow-up date Date of closure to data entry Date trial data considered complete Date analysis concluded |
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6 | Update | 2013/02/06 16:47:50 | Recruitment status |
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7 | Update | 2013/02/25 17:31:29 | Target sample size |
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8 | Update | 2013/02/25 17:33:56 | Date of closure to data entry |
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9 | Update | 2013/02/25 17:37:15 | Primary outcomes |
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10 | Update | 2013/02/25 17:40:48 | Recruitment status Date analysis concluded |