- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05012228
Molecular Mechanisms of Fibrillin/LTBP Superfamily in Renal Fibrosis and Cardiorenal Syndrome
April 15, 2024 updated by: National Taiwan University Hospital
Molecular Mechanisms of Fibrillin/LTBP Superfamily in Renal Fibrosis and Cardiorenal
This project is to understand the LTBP4 expression in human renal fibrotic tissues.
The investigators will exam major location of LTBP4 expression and check any similar or discrepancy in renal fibrosis with different etiologies.
Study Overview
Status
Recruiting
Conditions
Detailed Description
The investigators will obtain the residual renal tissues with different etiologies and check the expression of LTBP4.
The location and quantitation of LTBP4 in renal tissues will be checked.
It will be great to understand the association between the severity of fibrosis and the expression of LTBP4 and other matrix proteins.
Study Type
Observational
Enrollment (Estimated)
30
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Yue-Jhu Huang, MS
- Phone Number: +886912282113
- Email: yuejhuhuang@outlook.com
Study Contact Backup
- Name: Chi-Ting Su, MD, MPH, PhD
- Phone Number: +88697262878
- Email: A01218@ntucc.gov.tw
Study Locations
-
-
-
Taipei, Taiwan
- Recruiting
- National Taiwan University Hospital
-
Contact:
- Chi-Ting Su, MD. MPH. PhD
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Sampling Method
Probability Sample
Study Population
Subjects with chronic kidney disease, which has remaining specimens in NTUH.
The investigators want to use 2008-2016 specimens in Department of Pathology, NTUH.
Description
Inclusion Criteria:
- Abnormal kidney function, proteinuria, hematuria
Exclusion Criteria:
- N/A
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Other
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Expression of LTBP4 in human renal fibrotic tissue
Time Frame: 5 years
|
5 years
|
|
|
Expression of biomarkers in human renal fibrotic tissue
Time Frame: 5 years
|
Potential markers: eg.
ROS-related proteins (8-oxodG, 4-HNE)
|
5 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 1, 2021
Primary Completion (Actual)
March 1, 2022
Study Completion (Estimated)
December 31, 2024
Study Registration Dates
First Submitted
August 3, 2021
First Submitted That Met QC Criteria
August 16, 2021
First Posted (Actual)
August 19, 2021
Study Record Updates
Last Update Posted (Actual)
April 17, 2024
Last Update Submitted That Met QC Criteria
April 15, 2024
Last Verified
April 1, 2024
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 202101074RINC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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