UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000051368
Receipt number R000058605
Scientific Title Evaluation of the standard value of body composition by sex and age using abdominal CT scan images in patients visiting primary care hospital
Date of disclosure of the study information 2023/07/31
Last modified on 2023/06/16 22:09:37

* 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

Evaluation of the standard value of body composition by sex and age using abdominal CT scan images in patients visiting primary care hospital

Acronym

Evaluation of the standard value of body composition by sex and age using abdominal CT scan images in patients visiting primary care hospital

Scientific Title

Evaluation of the standard value of body composition by sex and age using abdominal CT scan images in patients visiting primary care hospital

Scientific Title:Acronym

Evaluation of the standard value of body composition by sex and age using abdominal CT scan images in patients visiting primary care hospital

Region

Japan


Condition

Condition

Patients who visited a primary care hospital (Tomei Hospital, Nagakute city, Aichi, Japan) and underwent abdominal CT scan. Among them, patients who agreed to participate a clinical study (UMIN000032577)for the evaluation of body composition using abdominal CT scan images.
scan.

Classification by specialty

Medicine in general

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the standard value of body composition by sex and age using abdominal CT scan images in patients visiting primary care hospital.

Basic objectives2

Others

Basic objectives -Others

To evaluate the correlation between the data of body composition and clinical characteristics and the data of blood test.

Trial characteristics_1

Others

Trial characteristics_2

Others

Developmental phase

Not applicable


Assessment

Primary outcomes

To evaluate the standard value of body composition by sex and age using abdominal CT scan images

Key secondary outcomes



Base

Study type

Others,meta-analysis etc


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 visited a primary care hospital (Tomei Hospital, Nagakute city, Aichi, Japan) and underwent abdominal CT
scan. Among them, patients who agreed to participate a previous clinical study (UMIN000032577) and who were measured body composition using abdominal CT scan images.These data are secondary used for the analysis.

Key exclusion criteria

not applicable

Target sample size



Research contact person

Name of lead principal investigator

1st name Yukihiro
Middle name
Last name Yokoyama

Organization

Nagoya University Graduate School of Medicine

Division name

Department of Surgery, Division of Perioperative Medicine

Zip code

466-8550

Address

65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, Japan

TEL

052-744-2222

Email

yyoko@med.nagoya-u.ac.jp


Public contact

Name of contact person

1st name Yukihiro
Middle name
Last name Yokoyama

Organization

Nagoya University Graduate School of Medicine

Division name

Department of Surgery, Division of Perioperative Medicine

Zip code

466-8550

Address

65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, Japan

TEL

052-744-2222

Homepage URL


Email

yyoko@med.nagoya-u.ac.jp


Sponsor or person

Institute

Nagoya University

Institute

Department

Personal name



Funding Source

Organization

Nagoya 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

Nagoya University Ethics Committee

Address

65 Tsurumai-cho, Showa-ku, Nagoya, Aichi, Japan

Tel

052-741-2111

Email

ethics@med.nagoya-u.ac.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1

0000000

Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2023 Year 07 Month 31 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

2023 Year 06 Month 16 Day

Date of IRB


Anticipated trial start date

2023 Year 07 Month 31 Day

Last follow-up date

2026 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Tomei Hospital


Management information

Registered date

2023 Year 06 Month 16 Day

Last modified on

2023 Year 06 Month 16 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000058605