| Recruitment status | Completed |
| Unique ID issued by UMIN | UMIN000045057 |
| Receipt No. | R000051431 |
| Scientific Title | Clinical study for premature ejaculation with Men's Training Cup Keep Training |
| Date of disclosure of the study information | 2021/08/04 |
| Last modified on | 2021/11/25 (Ver. 4) |
| Basic information | ||
| Public title | Clinical study for premature ejaculation with Men's Training Cup Keep Training | |
| Acronym | Clinical study for premature ejaculation with Men's Training Cup Keep Training | |
| Scientific Title | Clinical study for premature ejaculation with Men's Training Cup Keep Training | |
| Scientific Title:Acronym | Clinical study for premature ejaculation with Men's Training Cup Keep Training | |
| Region |
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| Condition | ||
| Condition | premature ejaculation | |
| Classification by specialty |
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| Classification by malignancy | Others | |
| Genomic information | NO | |
| Objectives | |
| Narrative objectives1 | improvement for premature ejaculation |
| Basic objectives2 | Efficacy |
| Basic objectives -Others | |
| Trial characteristics_1 | Confirmatory |
| Trial characteristics_2 | Explanatory |
| Developmental phase | Not applicable |
| Assessment | |
| Primary outcomes | IELT (Intravaginal Ejaculation Latency Time) |
| Key secondary outcomes | PEDT (Premature Ejaculation Diagnostic Tool)
SHIM (Sexual Health Inventory for Men) EHS (Erection Hardness Score) DPSIQ-5 (Difficulty in Performing Sexual Intercourse Questionnaire-5) |
| Base | |
| Study type | Observational |
| Study design | |
| Basic design | |
| Randomization | |
| Randomization unit | |
| Blinding | |
| Control | |
| Stratification | |
| Dynamic allocation | |
| Institution consideration | |
| Blocking | |
| Concealment | |
| Intervention | |
| No. of arms | |
| Purpose of intervention | |
| Type of intervention | |
| Interventions/Control_1 | |
| Interventions/Control_2 | |
| Interventions/Control_3 | |
| Interventions/Control_4 | |
| Interventions/Control_5 | |
| Interventions/Control_6 | |
| Interventions/Control_7 | |
| Interventions/Control_8 | |
| Interventions/Control_9 | |
| Interventions/Control_10 | |
| Eligibility | ||||
| Age-lower limit |
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| Age-upper limit |
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| Gender | Male | |||
| Key inclusion criteria | premature ejaculation | |||
| Key exclusion criteria | uncontrollable diabetes mellitus
neurogenic disease antidepressant drug alpha1-adrenergic receptor 5alpha-reductase inhibitor |
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| Target sample size | 100 | |||
| Research contact person | |||||||
| Name of lead principal investigator |
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| Organization | Juntendo University Urayasu Hospital | ||||||
| Division name | Department of Urology | ||||||
| Zip code | 2790021 | ||||||
| Address | 2-1-1 Tomioka, Urayasu city, Chiba, Japan | ||||||
| TEL | 0473533111 | ||||||
| atsujimu@juntendo.ac.jp | |||||||
| Public contact | |||||||
| Name of contact person |
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| Organization | Juntendo University Urayasu Hospital | ||||||
| Division name | Department of Urology | ||||||
| Zip code | 2790021 | ||||||
| Address | 2-1-1 Tomioka, Urayasu city, Chiba, Japan | ||||||
| TEL | 0473533111 | ||||||
| Homepage URL | |||||||
| masatos@juntendo-urayasu.jp | |||||||
| Sponsor | |
| Institute | Department of Urology, Juntendo University Urayasu Hospital |
| Institute | |
| Department | |
| Funding Source | |
| Organization | Juntendo University Urayasu Hospital |
| Organization | |
| Division | |
| Category of Funding Organization | Self funding |
| Nationality of Funding Organization | Japan |
| Other related organizations | |
| Co-sponsor | EAST clinic Shinjuku
EAST clinic Shinbashi |
| Name of secondary funder(s) | none |
| IRB Contact (For public release) | |
| Organization | Juntendo University Urayasu Hospital |
| Address | 2-1-1 Tomioka, Urayasu city, Chiba, Japan |
| Tel | 0473533111 |
| rinri-urayasu@juntendo-urayasu.jp | |
| Secondary IDs | |
| Secondary IDs | NO |
| Study ID_1 | |
| Org. issuing International ID_1 | |
| Study ID_2 | |
| Org. issuing International ID_2 | |
| IND to MHLW | |
| Institutions | |
| Institutions | 順天堂大学医学部附属浦安病院(千葉県)
イースト駅前クリニック新宿院(東京都) イースト駅前クリニック新橋院(東京都) |
| Other administrative information | |||||||
| Date of disclosure of the study information |
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| Related information | |
| URL releasing protocol | |
| Publication of results | Partially published |
| Result | |
| URL related to results and publications | |
| Number of participants that the trial has enrolled | 37 |
| Results | |
| Results date posted | |
| Results Delayed | |
| Results Delay Reason | |
| Date of the first journal publication of results | |
| Baseline Characteristics | |
| Participant flow | |
| Adverse events | |
| Outcome measures | |
| Plan to share IPD | |
| IPD sharing Plan description | |
| Progress | |||||||
| Recruitment status | Completed | ||||||
| Date of protocol fixation |
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| Date of IRB |
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| Anticipated trial start date |
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| Last follow-up date |
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| Date of closure to data entry |
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| Date trial data considered complete |
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| Date analysis concluded |
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| Other | |
| Other related information | study duration is 2-month |
| Management information | |||||||
| Registered date |
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| Last modified on |
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| Link to view the page | |
| URL(English) | https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000051431 |