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

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National Taiwan University

Status

Completed

Conditions

Arteriovenous Fistula Occlusion

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

NCT05832476
201712231RINC

Details and patient eligibility

About

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.

Full description

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.

Enrollment

126 patients

Sex

All

Ages

20+ years old

Volunteers

No Healthy Volunteers

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

Trial design

126 participants in 2 patient groups

Matured
Description:
It is defined as the target HDAVF can be used
Treatment:
Other: No intervention
Non-matured
Description:
RC-AVF underwent additional intervention after 90 days of observation
Treatment:
Other: No intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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