Name: UMIN ID:
Unique ID issued by UMIN | UMIN000021267 |
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Receipt number | R000024513 |
Scientific Title | Longitudinal Efficacy and Safety Study of Tolvaptan on Autosomal Dominant Polycystic Kidney Disease Patients |
Date of disclosure of the study information | 2016/03/12 |
Last modified on | 2021/03/09 10:50:59 |
No. | Disposal | Last modified on | Item of update | |
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1 | Insert | 2016/03/01 17:51:22 | ||
2 | Update | 2016/03/12 10:37:27 | Date of disclosure of the study information |
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3 | Update | 2016/03/23 19:16:06 | Acronym Acronym |
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4 | Update | 2016/03/23 20:34:02 | Acronym |
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5 | Update | 2016/08/12 10:40:23 | Name of primary person or sponsor Organization Research ethics review Secondary IDs Study ID_1 Org. issuing International ID_1 Org. issuing International ID_1 |
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6 | Update | 2016/08/12 11:09:40 | Key inclusion criteria Key inclusion criteria |
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7 | Update | 2016/08/12 11:11:57 | Date of protocol fixation Anticipated trial start date |
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8 | Update | 2016/08/12 11:40:09 | Anticipated trial start date |
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9 | Update | 2016/11/01 15:20:10 | Recruitment status Last follow-up date Date of closure to data entry Date analysis concluded |
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10 | Update | 2017/03/08 13:17:52 | Date of protocol fixation Last follow-up date Date of closure to data entry Date trial data considered complete Date analysis concluded |
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11 | Update | 2018/02/20 17:58:00 | Genomic information Narrative objectives1 Narrative objectives1 Trial characteristics_1 Trial characteristics_2 Developmental phase Primary outcomes Primary outcomes Key secondary outcomes Key secondary outcomes |
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12 | Update | 2018/02/20 19:04:14 | Stratification Interventions/Control_1 Interventions/Control_1 Key inclusion criteria Key inclusion criteria Key exclusion criteria Key exclusion criteria Target sample size |
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13 | Update | 2018/02/20 19:12:06 | Recruitment status Last follow-up date Date of closure to data entry Date trial data considered complete Date analysis concluded |
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14 | Update | 2018/02/20 19:14:32 | Primary outcomes |
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15 | Update | 2018/06/13 12:58:02 | Study type Basic design Randomization Blinding Control Stratification No. of arms Purpose of intervention Type of intervention Interventions/Control_1 Interventions/Control_1 |
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16 | Update | 2018/06/13 13:34:30 | Other related information Other related information |
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17 | Update | 2018/08/17 11:31:44 | Narrative objectives1 Narrative objectives1 Primary outcomes Primary outcomes |
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18 | Update | 2018/08/17 11:46:28 | Organization Organization Organization Organization Organization Organization Institute Institute |
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19 | Update | 2018/08/17 12:20:06 | Last follow-up date Date trial data considered complete Date analysis concluded |
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20 | Update | 2020/03/10 15:43:14 | Narrative objectives1 Narrative objectives1 Primary outcomes Primary outcomes |
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21 | Update | 2020/03/10 15:51:53 | 1st name of lead principal investigator Last name of lead principal investigator 1st name of lead principal investigator Last name of lead principal investigator Zip code Address Last name of contact person Last name of contact person Zip code Address Organization1 Organization2 Address2 Tel2 Email2 Organization Organization Address Address Tel Institutions |
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22 | Update | 2020/03/10 15:54:20 | Number of participants that the trial has enrolled |
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23 | Update | 2020/03/10 15:58:26 | Date of IRB |
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24 | Update | 2020/06/04 12:17:28 | Last follow-up date Date of closure to data entry Date trial data considered complete Date analysis concluded |
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25 | Update | 2021/03/09 10:50:59 | Recruitment status Date of closure to data entry Date trial data considered complete Date analysis concluded |