UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000038405
Receipt number R000043767
Scientific Title the relationship between physical function and adverse event in elderly patients undergoing peritoneal dialysis: a prospective cohort study.
Date of disclosure of the study information 2019/10/29
Last modified on 2022/05/06 11:28:53

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Basic information

Public title

the relationship between physical function and adverse event in elderly patients undergoing peritoneal dialysis: a prospective cohort study.

Acronym

the relationship between physical function and adverse event in elderly patients undergoing peritoneal dialysis: a prospective cohort study.

Scientific Title

the relationship between physical function and adverse event in elderly patients undergoing peritoneal dialysis: a prospective cohort study.

Scientific Title:Acronym

the relationship between physical function and adverse event in elderly patients undergoing peritoneal dialysis: a prospective cohort study.

Region

Japan


Condition

Condition

chronic kidney disease

Classification by specialty

Nephrology Rehabilitation medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study was to assess the physical function in elderly PD patients and investigate association between physical function and prognosis.

Basic objectives2

Safety,Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

overall mortality

Key secondary outcomes

Cardiovascular event, peritonitis, hospitalization, Withdrawal of peritoneal dialysis


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

65 years-old <=

Age-upper limit

90 years-old >

Gender

Male and Female

Key inclusion criteria

patients undergoing peritoneal dialysis
Patients with written informed consent after receiving a full explanation
Patients without apparent dementia

Key exclusion criteria

patient with hemodialysis
patient with renal transplant
Patient judged to be inappropriate by the charge doctor

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Hiroki
Middle name
Last name Yabe

Organization

Seirei christopher university

Division name

Department of Rehabilitation

Zip code

433-8558

Address

3453 Mikatahara, Kita-ku, Hamamatsu, Shizuoka.

TEL

0534391400

Email

yabe0909@gmail.com


Public contact

Name of contact person

1st name Yabe
Middle name
Last name Hiroki

Organization

Seirei christopher university

Division name

Department of Rehabilitation

Zip code

433-8558

Address

3453 Mikatahara, Kita-ku, Hamamatsu, Shizuoka.

TEL

0534391400

Homepage URL


Email

yabe0909@gmail.com


Sponsor or person

Institute

Nagoya Kyoritsu Hospital

Institute

Department

Personal name



Funding Source

Organization

japan society for the promoting of science

Organization

Division

Category of Funding Organization

Government offices of other countries

Nationality of Funding Organization



Other related organizations

Co-sponsor

Nagoya Kyoritsu Hospital

Name of secondary funder(s)



IRB Contact (For public release)

Organization

Seirei Christopher University

Address

3453 Mikatahara, kita-ku Hamamatsu, Shizuoka

Tel

0534391400

Email

yabe0909@gmail.com


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

名古屋共立病院(愛知県)


Other administrative information

Date of disclosure of the study information

2019 Year 10 Month 29 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

No longer recruiting

Date of protocol fixation

2016 Year 12 Month 01 Day

Date of IRB

2017 Year 02 Month 07 Day

Anticipated trial start date

2017 Year 04 Month 01 Day

Last follow-up date

2020 Year 12 Month 31 Day

Date of closure to data entry

2021 Year 11 Month 30 Day

Date trial data considered complete

2021 Year 12 Month 31 Day

Date analysis concluded

2022 Year 04 Month 30 Day


Other

Other related information

observation of adverse events in regular outpatient clinics


Management information

Registered date

2019 Year 10 Month 28 Day

Last modified on

2022 Year 05 Month 06 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000043767


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name