| Recruitment status | Completed |
| Unique ID issued by UMIN | UMIN000012477 |
| Receipt No. | R000012801 |
| Official scientific title of the study | Study of measurement of hemodynamic status by oscillometric method |
| Date of disclosure of the study information | 2013/12/04 |
| Last modified on | 2018/12/26 (Ver. 6) |
| Basic information | ||
| Official scientific title of the study | Study of measurement of hemodynamic status by oscillometric method
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| Title of the study (Brief title) | Study of measurement of hemodynamic status by oscillometric method | |
| Region |
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| Condition | ||
| Condition | Elective surgery patient over 20 yrs | |
| Classification by specialty |
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| Classification by malignancy | Malignancy | |
| Genomic information | NO | |
| Objectives | |
| Narrative objectives1 | Confirm the usefulness of the new measurement method of pulse pressure variation(PPV) and central venous pressure(CVP)
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| Basic objectives2 | Efficacy |
| Basic objectives -Others | |
| Trial characteristics_1 | Exploratory |
| Trial characteristics_2 | Pragmatic |
| Developmental phase | Phase I |
| Assessment | |
| Primary outcomes | Correlation between the ordinary pulse pressure variation calculated from arterial waveform and the pulse pressure variation which is estimated by our new method.
Correlation between ordinary central venous pressure and the central venous pressure which is estimated by our new method. |
| Key secondary outcomes | Safety of our method. |
| Base | |
| Study type | Interventional |
| Study design | |
| Basic design | Single arm |
| Randomization | Non-randomized |
| Randomization unit | |
| Blinding | Open -no one is blinded |
| Control | Uncontrolled |
| Stratification | |
| Dynamic allocation | |
| Institution consideration | |
| Blocking | |
| Concealment | |
| Intervention | ||
| No. of arms | 1 | |
| Purpose of intervention | Prevention | |
| Type of intervention |
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| Interventions/Control_1 | Duration: During the stay in operating room.
Frequency: 10 times or more at 10 minutes or more intervals. |
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| 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 | Patients who is planned measuring arterial pressure by arterial catheter or is planned measuring central venous pressure.
Patients who are given informed consent. |
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| Key exclusion criteria | Patients who cannot be attached pressure cuff at both upperarm by reason of surgical procedure or physical impairment.
Patients who withdrawn informed consent. |
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| Target sample size | 10 | |||
| Research contact person | |
| Name of lead principal investigator | Masashi Kawamoto |
| Organization | Division of Clinical Medical Science, Graduate School of Biomedical Sciences, Hiroshima University |
| Division name | Department of Anesthesiology and Critical Care |
| Address | 1-2-3,Kasumi,Minami-ku,Hiroshima |
| TEL | 081-082-256-3234 |
| anekawa@hiroshima-u.ac.jp | |
| Public contact | |
| Name of contact person | Ryuji Nakamura |
| Organization | Division of Clinical Medical Science, Graduate School of Biomedical Sciences, Hiroshima University |
| Division name | Department of Anesthesiology and Critical Care |
| Address | 1-2-3,Kasumi,Minami-ku,Hiroshima |
| TEL | 081-082-256-3234 |
| Homepage URL | |
| r-nacamura@hiroshima-u.ac.jp | |
| Sponsor | |
| Institute | Department of Anesthesiology and Critical Care, Division of Clinical Medical Science, Graduate School of Biomedical Sciences, Hiroshima University |
| Institute | |
| Department | |
| Funding Source | |
| Organization | None |
| Organization | |
| Division | |
| Category of Funding Organization | Self funding |
| Nationality of Funding Organization | |
| Other related organizations | |
| Co-sponsor | NIHON KOHDEN CORPORATION |
| Name of secondary funder(s) | |
| 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 | 広島大学病院(広島県) |
| Other administrative information | |||||||
| Date of disclosure of the study information |
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| Progress | |||||||
| Recruitment status | Completed | ||||||
| Date of protocol fixation |
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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 | |||||||
| Related information | |
| URL releasing protocol | |
| Publication of results | Published |
| URL releasing results | |
| Results | |
| Other related information | |
| 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=R000012801 |