UMIN-CTR Clinical Trial

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

Name:
UMIN ID:

Recruitment status Terminated
Unique ID issued by UMIN UMIN000030763
Receipt No. R000035128
Scientific Title Clinical factors affecting massive blood transfusion in ruptured aortic abdominal aneurysm surgery
Date of disclosure of the study information 2018/01/12
Last modified on 2019/07/18

* 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 Clinical factors affecting massive blood transfusion in ruptured aortic abdominal aneurysm surgery
Acronym Clinical factors affecting massive blood transfusion in ruptured aortic abdominal aneurysm surgery
Scientific Title Clinical factors affecting massive blood transfusion in ruptured aortic abdominal aneurysm surgery
Scientific Title:Acronym Clinical factors affecting massive blood transfusion in ruptured aortic abdominal aneurysm surgery
Region
Japan

Condition
Condition surgical patients with ruptured abdominal aortic aneurysm
Classification by specialty
Vascular surgery Anesthesiology Cardiovascular surgery
Blood transfusion
Classification by malignancy Others
Genomic information NO

Objectives
Narrative objectives1 The aim of the study is to determine clinical factors for the prediction of total volume of transfusion.
Basic objectives2 Efficacy
Basic objectives -Others
Trial characteristics_1 Confirmatory
Trial characteristics_2 Explanatory
Developmental phase Not applicable

Assessment
Primary outcomes Total volume of blood transfusion during surgery
Key secondary outcomes

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

Not applicable
Age-upper limit

Not applicable
Gender Male and Female
Key inclusion criteria Surgical patient for repair of ruptured abdominal aortic aneurysm
Key exclusion criteria None
Target sample size 120

Research contact person
Name of lead principal investigator
1st name Shigekazu
Middle name
Last name Sugino
Organization Tohoku University
Division name Department of Anesthesiology and Perioperative Medicine
Zip code 9800875
Address 2-1, Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8575, Japan
TEL 0227177321
Email sugino@ruby.ocn.ne.jp

Public contact
Name of contact person
1st name Shigekazu
Middle name
Last name Sugino
Organization Tohoku University
Division name Department of Anesthesiology and Perioperative Medicine
Zip code 9800875
Address 2-1, Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8575, Japan
TEL 0227177321
Homepage URL
Email sugino@ruby.ocn.ne.jp

Sponsor
Institute Tohoku University
Institute
Department

Funding Source
Organization Self funding
Organization
Division
Category of Funding Organization Self funding
Nationality of Funding Organization

Other related organizations
Co-sponsor
Name of secondary funder(s)

IRB Contact (For public release)
Organization Tohoku University School of Medicine IRB
Address 2-1, Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8575, Japan
Tel 0227284105
Email med-kenkyo@grp.tohoku.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
2018 Year 01 Month 12 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 48
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 Terminated
Date of protocol fixation
2018 Year 01 Month 11 Day
Date of IRB
2018 Year 02 Month 22 Day
Anticipated trial start date
2018 Year 02 Month 24 Day
Last follow-up date
2019 Year 01 Month 14 Day
Date of closure to data entry
Date trial data considered complete
Date analysis concluded

Other
Other related information We assigned 48 patients to the trial. However, we stopped the study because there was not any difference in the population.

Management information
Registered date
2018 Year 01 Month 11 Day
Last modified on
2019 Year 07 Month 18 Day


Link to view the page
URL(English) https://upload.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000035128

Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name


Contact us.