UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000030342 |
|---|---|
| Receipt number | R000034651 |
| Scientific Title | Association of clinical parameters with pathological findings in patients with chronic kidney disease (CKD) who underwent kidney biopsy: a cross-sectional study. |
| Date of disclosure of the study information | 2017/12/11 |
| Last modified on | 2019/05/16 16:31:35 |
* 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
Association of clinical parameters with pathological findings in patients with chronic kidney disease (CKD) who underwent kidney biopsy: a cross-sectional study.
Acronym
Association of clinical parameters with pathological findings in CKD patients who underwent kidney biopsy.
Scientific Title
Association of clinical parameters with pathological findings in patients with chronic kidney disease (CKD) who underwent kidney biopsy: a cross-sectional study.
Scientific Title:Acronym
Association of clinical parameters with pathological findings in CKD patients who underwent kidney biopsy.
Region
| Japan |
Condition
Condition
Chronic kidney disease
Classification by specialty
| Nephrology |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To elucidate the association of clinical parameters with pathological findings in CKD patients who underwent kidney biopsy.
Basic objectives2
Others
Basic objectives -Others
This study is a cross-sectional one based on clinical data in each patient.
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
To explore the factors associated with pathological features in CKD patients who underwent kidney biopsy.
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
| 20 | years-old | <= |
Age-upper limit
| 999 | years-old | >= |
Gender
Male and Female
Key inclusion criteria
Patients who were admitted to our hospital for kidney biopsy since June 2009 and gave written-informed consent.
Key exclusion criteria
1. Patients who did not give informed consent
2.Patients who experienced acute exacerbation of kidney disease
Target sample size
99999
Research contact person
Name of lead principal investigator
| 1st name | MASARU |
| Middle name | |
| Last name | NAKAYAMA |
Organization
National Hospital Organization
Kyushu Medical Center
Division name
Nephrology
Zip code
810-8563
Address
1-8-1 Jigyohama, Chuo-Ku, Fukuoka 810-8563, Japan
TEL
092-852-0700
nakayama.masaru.kv@mail.hosp.go.jp
Public contact
Name of contact person
| 1st name | MASARU |
| Middle name | |
| Last name | NAKAYAMA |
Organization
National Hospital Organization Kyushu Medical Center
Division name
Nephrology
Zip code
810-8563
Address
1-8-1 Jigyohama, Chuo-Ku, Fukuoka 810-8563, Japan
TEL
092-852-0700
Homepage URL
nakayama.masaru.kv@mail.hosp.go.jp
Sponsor or person
Institute
National Hospital Organization
Kyushu Medical Center
Institute
Department
Personal name
Funding Source
Organization
National Hospital Organization
Kyushu 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
National Hospital Organization Kyushu Medical Center research ethics committee
Address
1-8-1 Jigyohama, Chuo-Ku, Fukuoka 810-8563, Japan
Tel
092-852-0700
nakayama.masaru.kv@mail.hosp.go.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 | 12 | Month | 11 | 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
Enrolling by invitation
Date of protocol fixation
| 2009 | Year | 06 | Month | 01 | Day |
Date of IRB
| 2009 | Year | 05 | Month | 27 | Day |
Anticipated trial start date
| 2009 | Year | 06 | Month | 01 | Day |
Last follow-up date
| 2030 | Year | 05 | Month | 31 | Day |
Date of closure to data entry
Date trial data considered complete
Date analysis concluded
Other
Other related information
Prospective study
Consecutive sampling
Management information
Registered date
| 2017 | Year | 12 | Month | 11 | Day |
Last modified on
| 2019 | Year | 05 | Month | 16 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000034651
