UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000054657
Receipt number R000062457
Scientific Title Predictive modeling of intraoperative bleeding and blood transfusion using the University of Tsukuba Hospital perioperative dataset
Date of disclosure of the study information 2024/06/14
Last modified on 2024/06/13 17:16:45

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Basic information

Public title

Predictive modeling of intraoperative bleeding and blood transfusion using the University of Tsukuba Hospital perioperative dataset

Acronym

Predictive modeling of intraoperative bleeding and blood transfusion

Scientific Title

Predictive modeling of intraoperative bleeding and blood transfusion using the University of Tsukuba Hospital perioperative dataset

Scientific Title:Acronym

Predictive modeling of intraoperative bleeding and blood transfusion

Region

Japan


Condition

Condition

Surgery under general anesthesia, epidural anesthesia, or spinal anesthesia

Classification by specialty

Anesthesiology Operative medicine Blood transfusion

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To create a model to predict the amount of blood loss and transfusion during surgery from preoperative information by using the University of Tsukuba Hospital perioperative dataset.

Basic objectives2

Others

Basic objectives -Others

To create a model to predict the amount of blood loss

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Amount of blood loss

Key secondary outcomes

transfusion or no transfusion, amount of blood transfusion


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

Patients who underwent surgery under general, epidural, or spinal anesthesia at the University of Tsukuba Hospital from April 1, 2012 to March 31, 2023.

Key exclusion criteria

Second or subsequent surgeries during hospitalization. Patients with missing or erroneous data.

Target sample size

70000


Research contact person

Name of lead principal investigator

1st name Nanako
Middle name
Last name Tamiya

Organization

University of Tsukuba

Division name

Department of Health Services Research, Faculty of Medicine

Zip code

305-8575

Address

1-1-1 Tenno-dai, Tsukuba, Ibaraki, Japan

TEL

+81-(0)29-853-8849

Email

hsr@md.tsukuba.ac.jp


Public contact

Name of contact person

1st name Kensuke
Middle name
Last name Shimada

Organization

University of Tsukuba

Division name

Tsukuba Clinical Research & Development Organization

Zip code

2-1-1

Address

2-1-1 Amakubo, Tsukuba, Ibaraki, Japan

TEL

+81-29-853-3914

Homepage URL


Email

kensukeshimada.s@gmail.com


Sponsor or person

Institute

University of Tsukuba

Institute

Department

Personal name



Funding Source

Organization

None

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

University of Tsukuba Hospital

Address

2-1-1 Amakubo, Tsukuba, Ibaraki 305-8576, Japan

Tel

+81-29-853-3914

Email

kensukeshimada.s@gmail.com


Secondary IDs

Secondary IDs

YES

Study ID_1

R05-219

Org. issuing International ID_1

University of Tsukuba Hospital

Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2024 Year 06 Month 14 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

Preinitiation

Date of protocol fixation

2024 Year 04 Month 05 Day

Date of IRB

2024 Year 05 Month 07 Day

Anticipated trial start date

2024 Year 06 Month 14 Day

Last follow-up date

2027 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

This study uses the dataset created by the "Large-scale observational study on the quality of perioperative care using perioperative dataset from the University of Tsukuba Hospital (R03-068)".


Management information

Registered date

2024 Year 06 Month 13 Day

Last modified on

2024 Year 06 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000062457