Delivery of Inhibitors of Lysyl Oxidase (LysoLox) on Serial Angioplasty and Time to Restenosis

Arteriovenous Fistula Occlusion Clinical Trial

Official title:

Balloon Angioplasty of Dialysis AV Fistulae: Effect of Local Delivery of Inhibitors of Lysyl Oxidase (LysoLox) on Serial Angioplasty and Time to Restenosis

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03106948
• Other study ID #: Lysyl Oxidase (LysoLox)
• Status: Recruiting
• Phase: Phase 2
• First received: February 15, 2017
• Last updated: September 6, 2017
• Start date: February 1, 2017
• Est. completion date: March 2018

Study information

• Verified date: September 2017
• Source: Southeast Renal Research Institute
• Contact: James A Tumlin, MD
• Phone: 423-290-0882
• Email: jamestumlinmd[@]nephassociates.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The narrowing of Dialysis Fistulae or Grafts is a near universal problem in patients with end-stage renal disease (ESRD) and requires patients to undergo repeated angioplasty or mechanical opening of the fistula.

Description:

The failure of dialysis accesses remains a leading cause of morbidity and medical costs among ESRD subjects. The underlying etiology for dialysis access failure is uniformly due to progressive narrowing of the vessel lumen leading to stasis and thrombosis of the access. The luminal narrowing of arteriovenous fistulae (AVFs) is due to progressive hyperplasia of vessel intima and subsequent infiltration of smooth muscle cells into the vessel media. Areas of stenosis within AVFs are characterized by dense neointimal hyperplasia, infiltration of vascular smooth muscle cells and expansion of extracellular matrix material. Additionally, varying types of vascular injury increase the rate of collagen and elastin deposition within the medial and serosal areas of the vessel.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 30
• Est. completion date: March 2018
• Est. primary completion date: January 31, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 90 Years

Eligibility

Inclusion Criteria:

• Age 18 and < 90 years old

• Receiving stable out-subject hemodialysis for a minimum of 3 months

• Have a lower arm or upper arm AVF that has been cleared for use by the vascular surgeon or interventional nephrologist

• Have agreed to participate voluntarily and signed and dated an IRB approved, subject informed consent form

• Dysfunctional Dialysis Fistula: Any subject with

• Two or more venous pressure readings exceeding 250 mmHg for a minimum of 5 minutes at a blood flow of 500mls/min within a single dialysis run AND a documented reduction in KT/V by > 0.2; OR

• Patients with venous pressures > 250 mm Hg on two or more days within a 30 day period OR

• Patients who on physical exam are found to have palpable obstructions, post-stenotic dilation of the access or evidence of prolonged post-dialysis bleeding.

• Any patient with one of the above conditions will be to have a dysfunctional AVF. This definition will be applied to the screening of study subjects as well as the determination of recurrent fistula dysfunction at 12 months.

Exclusion Criteria:

• Scheduled for surgical revision of the fistula;

• Have been in another investigational (non-approved) drug or device study within the previous 30 days;

**have a known allergy to any component of the investigational product (drug or device)

• Subjects with a "Hero Graft" will be excluded from the study

• Subjects having received a stent for correction of a prior stenosis will be excluded from the trial

• Subjects with more than > 3 hemodynamically significant stenosis at one time (with the exception of a central venous stenosis)

• Subjects who are pregnant will be excluded from the trial (pregnancy test will be performed on subjects of child bearing potential). A urine pregnancy test will be utilized.

Related Conditions & MeSH terms

• Arteriovenous Fistula
• Arteriovenous Fistula Occlusion
• Fistula

Intervention

Drug:
• Placebo
Subject will undergo endoluminal biopsy prior to angioplasty but will NOT undergo insertion of the ACT drug delivery catheter
• Ascorbic Acid
Subject will undergo endoluminal biopsy prior to angioplasty followed by insertion of the ACT drug delivery catheter where ascorbic acid (10.0 µM) will be injected following conventional balloon angioplasty
• Cuprimine Oral Product
Subject will undergo endoluminal biopsy prior to angioplasty followed by insertion of the ACT drug delivery catheter where ascorbic acid (10.0 µM) in combination with D-penicillamine (25 µM) will be injected following conventional balloon angioplasty

Locations

Country	Name	City	State
United States	Southeast Renal Research Institute	Chattanooga	Tennessee

Sponsors (2)

Lead Sponsor	Collaborator
Southeast Renal Research Institute	Dialysis Clinic, Inc.

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Patients treated with ascorbic acid in combination with D-penicillamine will have longer periods between serial angioplasties over 12-month period. Additionally, subjects receiving combination therapy may have greater post-angioplasty luminal diameters.	Subjects are followed for 12 months and monitored for signs of fistula dysfunction. When the patient's fistula becomes dysfunctional they will be referred for a fistulogram. The time between serial fistulograms will be recorded as a secondary endpoint. Patients who are referred for a repeat fistulogram and having a luminal narrowing of greater than 70% will undergo a second intimal biopsy.	12 months