O-GlcNac Modified Proteomics Study of the Maturation of Hemodialysis Arteriovenous

NCT ID: NCT05832476

Last Updated: 2023-04-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

126 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-03-28

Study Completion Date

2020-10-26

Brief Summary

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We divided into three parts to carry out. Firstly, evidence the pre-existing fibrosis in vein of AVF failure patients. investigation of expression, the role, and the mechanism by which the identified O-GlcNAac proteins promote, maturation of AV fistula. Finally, ddress and compare the proteomics differentiation between failure and maturation of AVF patients.

Detailed Description

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End stage renal disease (ESRD) patients requires hemodialysis to maintain bloodstream functions. Before the hemodialysis, the patients requires a long-term vascular access, which best choice is Arteriovenous fistulas (AVF). However, 1/3 of patients were failure in AVF maturation, and it is still unknown. Our preliminary data have shown that pre-exisiting fibrosis in vein of AVF failure. Here, we will investigate whether pre-existing fibrosis of vein is asssociated with circulating fibrocytes in AVF failure, and further to address molecular mechanism of fibrocytes differentiation. We will divide into three parts to carry out. Firstly, evidence the pre-existing fibrosis in vein of AVF failure patients. Secondary, investigation of expression, the role, and the mechanism by which the identified O-GlcNAac proteins promote, maturation of AV fistula. Finally, address and compare the proteomics differentiation between failure and maturation of AVF patients. We hope that through this project, we can obtain signifiture molecules for precision detection and solve the current clinical unmet need.

Conditions

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Arteriovenous Fistula Occlusion

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Matured

It is defined as the target HDAVF can be used

No intervention

Intervention Type OTHER

No intervention

Non-matured

RC-AVF underwent additional intervention after 90 days of observation

No intervention

Intervention Type OTHER

No intervention

Interventions

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No intervention

No intervention

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Age of 20 and older adult patients, and preoperatively clinical and ultrasound assessment of the arm vessels are fisible for the creation of a native HDAVF that include:the augmented diameters of the veins is \> 2.0 mm and the diameter of the radial artery is\> 2.0 mm. Besides, there is no obvious stenosis of vessels in the forearm.

Exclusion Criteria

* The patient refused to join the study
* Too weak
* Serious heart failure
* Unconsciousness
* Bedridden for long time
* systemic lupus erythematosus(SLE), or other known autoimmune diseases
* The physician excludes the possibility of creating a wrist HDAVF before surgery
* Surgeon preoperatively identifies vessel inadequacy for the creation of a wrist HDAVF
* Choose a site other than the wrist for surgery
* Unexpected negative complications happen during surgery that prevent the completion of a wirst HDAVF
Minimum Eligible Age

20 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Taiwan University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Chih-Yang Chan, phd

Role: PRINCIPAL_INVESTIGATOR

National Taiwan University Hospital

Locations

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National Taiwan University Hospital

Taipei, No.7, Chung Shan S. Rd, Taiwan

Site Status

Countries

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Taiwan

Other Identifiers

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201712231RINC

Identifier Type: -

Identifier Source: org_study_id

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