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Clinical Trials/NCT07058441
NCT07058441Active, not recruitingNot Applicable

Clinical and Mechanistic Research on Autogenous Arteriovenous Fistula in Hemodialysis Patients

Ai Peng1 site in 1 country100 target enrollmentStarted: October 1, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Active, not recruiting
Sponsor
Enrollment
100
Locations
1
Primary Endpoint
Arteriovenous fistula maturation failure rate

Study Overview

Brief Summary

This study aims to investigate the long-term clinical outcomes and molecular mechanisms of autogenous arteriovenous fistula (AVF) maturation failure in uremic patients. The primary goal is to develop a precision prediction model integrating clinical, imaging, and biomarker data, while secondary objectives focus on identifying key molecular targets regulating AVF maturation.

Detailed Description

This observational study aims to investigate the long-term clinical outcomes and molecular mechanisms underlying autogenous arteriovenous fistula (AVF) maturation failure in uremic patients, with the primary goal of developing a precision prediction model integrating clinical, imaging, and biomarker data while also identifying key molecular targets regulating AVF maturation. Conducted as a single-center prospective study at Shanghai Tenth People's Hospital, the research will enroll 300 ESRD patients undergoing first-time AVF creation, collecting comprehensive multi-omics data including clinical parameters (demographics, comorbidities, laboratory tests), ultrasound imaging (vessel diameter, blood flow measurements), and molecular biomarkers (miRNAs, cytokines, vascular remodeling proteins). Using advanced machine learning techniques like Random Forest and XGBoost, the study will construct a predictive model for AVF maturation failure based on KDOQI criteria (blood flow <600 mL/min, diameter <6 mm, or depth >6 mm at 6 weeks), while parallel mechanistic investigations will employ WGCNA and Cox regression analyses to elucidate critical molecular pathways such as VEGF/TGF-β signaling and potential therapeutic targets including ALPL and Eph-B4. The study adheres to strict ethical guidelines (Helsinki Declaration, GCP standards) and includes rigorous statistical planning with a sample size calculated to ensure adequate power (300 patients yielding 110 expected events), employing AUC analysis for model discrimination and standard statistical tests for group comparisons. Expected outcomes include the development of a clinically applicable prediction tool (targeting software copyright), 2-3 high-impact SCI publications, and identification of novel therapeutic targets, with the entire project spanning from patient recruitment (2025.07-2026.07) through data analysis and manuscript preparation (2026.11-2027.01), ultimately aiming to significantly improve AVF management through its innovative combination of multi-omics integration and machine learning approaches.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age ≥18 years
  • •Diagnosed with chronic kidney disease stage 5 (ESRD) and scheduled for first-time autogenous AVF creation
  • •No severe coagulation disorders or vascular malformations
  • •Willing to provide written informed consent
  • •Planned hemodialysis at the study center

Exclusion Criteria

  • •Previous AVF surgery on the ipsilateral limb
  • •Ipsilateral central venous stenosis or significant venous outflow obstruction
  • •Active malignancy (except localized non-melanoma skin cancer)
  • •Active infection at the surgical site
  • •Life expectancy <1 year
  • •Pregnancy or lactation
  • •Participation in other interventional trials

Outcomes

Primary Outcomes

Arteriovenous fistula maturation failure rate

Time Frame: 6 weeks and 6 months post-surgery

Failure to meet KDOQI criteria at 6 weeks post-operation (blood flow \<600 mL/min, venous diameter \<6 mm, OR subcutaneous depth \>6 mm) AND inability to sustain hemodialysis (2 sessions/week)

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor
Ai Peng
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Ai Peng

Director of the department of Nephrology

Shanghai 10th People's Hospital

Study Sites (1)

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