UMIN-CTR Clinical Trial

BACK TOP
UMIN-CTR English Home Glossary (Simple) FAQ Search clinical trials

Name:
UMIN ID:

Recruitment status Completed
Unique ID issued by UMIN UMIN000026834
Receipt No. R000030794
Scientific Title the comparing inibp with nibp
Date of disclosure of the study information 2017/04/04
Last modified on 2019/04/23

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information
Public title the comparing inibp with nibp
Acronym the comparing inibp with nibp
Scientific Title the comparing inibp with nibp
Scientific Title:Acronym the comparing inibp with nibp
Region
Japan

Condition
Condition the patients who will have operationa
Classification by specialty
Anesthesiology
Classification by malignancy Malignancy
Genomic information NO

Objectives
Narrative objectives1 we will compare the speed of mesuring blood pressure using inibp with nibp
Basic objectives2 Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase

Assessment
Primary outcomes blood pressure measuring time
Key secondary outcomes

Base
Study type Interventional

Study design
Basic design Cross-over
Randomization Randomized
Randomization unit Individual
Blinding Single blind -participants are blinded
Control No treatment
Stratification YES
Dynamic allocation YES
Institution consideration Institution is considered as adjustment factor in dynamic allocation.
Blocking YES
Concealment Numbered container method

Intervention
No. of arms 2
Purpose of intervention Treatment
Type of intervention
Device,equipment
Interventions/Control_1 the patients will be divided in 2 groups in random. we will measure blood pressure using nibp with one group and inibp with the other.

we will compare the speed of measuring.
Interventions/Control_2 the patients will be divided in 2 groups in random. we will measure blood pressure using nibp with one group and inibp with the other.

we will compare the speed of measuring.
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
20 years-old <=
Age-upper limit

Not applicable
Gender Male and Female
Key inclusion criteria the patients who can accept the consent of this research.
Key exclusion criteria the patients who had the operation of breast cancer or who would have the operation of breast cancer.
Target sample size 66

Research contact person
Name of lead principal investigator
1st name Yasuhisa
Middle name
Last name Okuda
Organization dokkyo medical university Saitama medical center
Division name anesthesiology
Zip code 343-8555
Address 2-1-50,Minami koshigaya, Koshigaya city, Saitama
TEL +81-4-8965-1111
Email y-okuda@dokkyomed.ac.jp

Public contact
Name of contact person
1st name Kei
Middle name
Last name Takahashi
Organization dokkyo medical university saitama medical center
Division name anesthesiology
Zip code 343-8555
Address 2-1-50,Minami koshigaya, Koshigaya city, Saitama
TEL +81-4-8965-1111
Homepage URL
Email kkk14364@yahoo.co.jp

Sponsor
Institute dokkyo medical university saitama medical center
Institute
Department

Funding Source
Organization dokkyo medical university saitama medical center
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 dokkyo medical university saitama medical center
Address 2-1-50 Minamikoshigaya Koshigaya-city Saitama-Ken
Tel 048-965-0658
Email m-iyama@dokkyomed.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
2017 Year 04 Month 04 Day

Related information
URL releasing protocol
Publication of results Unpublished

Result
URL related to results and publications
Number of participants that the trial has enrolled
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
2017 Year 02 Month 14 Day
Date of IRB
Anticipated trial start date
2017 Year 04 Month 10 Day
Last follow-up date
2018 Year 08 Month 13 Day
Date of closure to data entry
2018 Year 08 Month 13 Day
Date trial data considered complete
2018 Year 08 Month 13 Day
Date analysis concluded
2018 Year 10 Month 01 Day

Other
Other related information

Management information
Registered date
2017 Year 04 Month 03 Day
Last modified on
2019 Year 04 Month 23 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000030794

Research Plan
Registered date File name
2018/09/27 INIBP 研究計画書 20180226.doc

Research case data specifications
Registered date File name

Research case data
Registered date File name


Contact us.