| Recruitment status | No longer recruiting |
| Unique ID issued by UMIN | UMIN000038442 |
| Receipt No. | R000043794 |
| Scientific Title | Clinical characteristics and morphological culprit plaque features in patients with acute coronary syndrome |
| Date of disclosure of the study information | 2019/10/30 |
| Last modified on | 2019/10/30 (Ver. 1) |
| Basic information | ||
| Public title | Clinical characteristics and morphological culprit plaque features in patients with acute coronary syndrome | |
| Acronym | Clinical characteristics and morphological culprit plaque features in patients with acute coronary syndrome | |
| Scientific Title | Clinical characteristics and morphological culprit plaque features in patients with acute coronary syndrome | |
| Scientific Title:Acronym | Clinical characteristics and morphological culprit plaque features in patients with acute coronary syndrome | |
| Region |
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| Condition | ||
| Condition | Acute coronary syndrome(ACS) | |
| Classification by specialty |
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| Classification by malignancy | Others | |
| Genomic information | NO | |
| Objectives | |
| Narrative objectives1 | The purpose of this study is to compare the morphological plaque features by age and gender in patients with ACS, and to find out the relationship with patient characteristics and prognosis. |
| Basic objectives2 | Bio-equivalence |
| Basic objectives -Others | |
| Trial characteristics_1 | |
| Trial characteristics_2 | |
| Developmental phase | |
| Assessment | |
| Primary outcomes | Presence of Plaque rupture, Erosion, or Calculated nodule in optical coherence tomography(OCT) findings of patients with ACS |
| Key secondary outcomes | Morphological features by age and gender of OCT findings in patients with ACS |
| 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 and Female | |||
| Key inclusion criteria | ACS patients who underwent pre-intervention optical coherence tomography | |||
| Key exclusion criteria | Cases of stent restenosis, stent thrombosis, and poor blood cell removal | |||
| Target sample size | 500 | |||
| Research contact person | |||||||
| Name of lead principal investigator |
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| Organization | Kobe University Graduate School of Medicine | ||||||
| Division name | Division of Cardiovascular Medicine | ||||||
| Zip code | 6500017 | ||||||
| Address | 7-5-2 Kusunoki-cho, Chuo-ku, Kobe | ||||||
| TEL | 0783825846 | ||||||
| hotake@med.kobe-u.ac.jp | |||||||
| Public contact | |||||||
| Name of contact person |
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| Organization | Kobe University Graduate School of Medicine | ||||||
| Division name | Division of Cardiovascular Medicine | ||||||
| Zip code | 6500017 | ||||||
| Address | 7-5-2 Kusunoki-cho, Chuo-ku, Kobe | ||||||
| TEL | 0783825846 | ||||||
| Homepage URL | |||||||
| hotake@med.kobe-u.ac.jp | |||||||
| Sponsor | |
| Institute | Kobe University |
| Institute | |
| Department | |
| Funding Source | |
| Organization | Kobe University |
| Organization | |
| Division | |
| Category of Funding Organization | Other |
| Nationality of Funding Organization | |
| Other related organizations | |
| Co-sponsor | |
| Name of secondary funder(s) | |
| IRB Contact (For public release) | |
| Organization | Kobe university hospital clinical and translational reserch center |
| Address | 7-5-2 Kusunoki-cho, Chuo-ku, Kobe |
| Tel | 0783826669 |
| ccrspprt@med.kobe-u.ac.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 | |
| Other administrative information | |||||||
| Date of disclosure of the study information |
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| Related information | |
| URL releasing protocol | |
| Publication of results | Unpublished |
| Result | |
| URL related to results and publications | |
| Number of participants that the trial has enrolled | 443 |
| 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 | No longer recruiting | ||||||
| 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 trial data considered complete | |||||||
| Date analysis concluded | |||||||
| Other | |
| Other related information | Retrospective multi centers registry
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| 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=R000043794 |