Paclitaxel for the Treatment of Distal Radial Artery Arteriovenous Access Fistula Stenosis (PaciFIST-2)

NCT ID: NCT02040454

Last Updated: 2015-02-02

Basic Information

• Recruitment Status: WITHDRAWN
• Clinical Phase: PHASE2
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-03-31
• Study Completion Date: 2016-10-31

Brief Summary

The objective of this study is to evaluate the safety and effectiveness of the use of intravascular paclitaxel, in addition to standard therapy, for the treatment of arteriovenous dialysis access fistula stenosis.

A fistulogram will be performed in standard fashion. The diagnostic component will include evaluation of the inflow artery, arterial anastomosis and full length of the fistula vein or graft, plus venous return up to the heart. The location, vessel size, lesion diameter and percent stenosis for each lesion will be recorded. Enrollment and randomization will occur at this point.

All patients will then receive standard therapy for their stenosis. This will include intravenous heparin administered in a standard dose of 70 units/kg. Lesions that respond poorly to angioplasty (>30% residual stenosis after angioplasty treatment with 2 inflations) will be stented. Stent selection will be based on clinical setting. Initial stent treatment will utilize an uncovered nitinol stent. Treatment of in-stent restenosis will include initial balloon angioplasty, and use of a covered stent (Viabahn, GORE, or Fluency, Bard). Documentation of location and type of treatment for each lesion treated will be recorded.

Once standard treatment is completed, the operating surgeon will be informed of the results of randomization: treatment (paclitaxel) or control. For subjects assigned to treatment, the whole fistula vein outflow segment of the fistula will be treated with paclitaxel.

The full length of the radial artery from 1 cm of its origin to fistula anatomosis will be treated with paclitaxel. In addition the anastomosis and first 4 cm of the fistula vein will be treated. Paclitaxel solution treatment of each lesion encountered will be attempted until the 20 mg Paclitaxel dose limit is met. The volume administered will depend on the diameter and length of the vessels treated. Maximization of the length of vessel and lesions treated will be undertaken when there are more lesions than can be accommodated by the 12 mg, 10 ml dose available.

A 5 F sheath, 20 cm in length, will be used to administer the paclitaxel. This will be advanced from its distal position in the radial artery over the guidewire so that the tip of the sheath is in the proximal radial artery.

Prior to removal of the sheath, a final angiographic study of all areas treated is performed to document patency and lesion appearance. Any additional lesions identified with this study are then treated appropriately following standard technique.

For the control group, instead of paclitaxel administration, a sham treatment period of 10 minutes is allowed to elapse followed by the performance of the final completion angiogram. Any additional lesions identified with this study are then treated appropriately following standard technique.

All patients will follow the same follow up evaluation schedule

Conditions

Arteriovenous Access Fistula Stenosis

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Study Groups

Standard Therapy Plus Paclitaxel

Standard Therapy - heparin, angioplasty, stent

Paclitaxel - single intravascular dose up to 20 mg

Group Type: ACTIVE_COMPARATOR

Paclitaxel

Intervention Type: DRUG

Standard Therapy

Intervention Type: PROCEDURE

Standard Therapy Alone

heparin, angioplasty, stent

Group Type: SHAM_COMPARATOR

Standard Therapy

Intervention Type: PROCEDURE

Interventions

Paclitaxel

Intervention Type: DRUG

Standard Therapy

Intervention Type: PROCEDURE

Other Intervention Names

Taxol

Eligibility Criteria

Inclusion Criteria

• Age 18 years or older
• Patient or guardian able to provide a signed informed consent
• Stenosis of the radial artery or initial 4 cm of the cephalic or basilic vein fistula with the anastomosis in the wrist greater than or equal to 50% treated satisfactorily (less than 20% residual stenosis) with balloon angioplasty alone or balloon angioplasty and stent placement
• Secondary fistulogram: the patient will have at least one prior fistulogram of the fistula to be treated.
• Either gender

Exclusion Criteria

• Women who are pregnant or who are expected to or might become pregnant
• Women of child-bearing potential who do not use contraception
• Life expectancy less than 12 months
• Known allergy to paclitaxel
• Known allergy to contrast media not previously demonstrated to be controllable with premedication on a prior study using contrast
• Known allergy to the pre-medications (dexamethasone, famotidine, diphenhydramine)
• Pre-fistulogram thrombosis of the fistula
• Thrombectomy of the fistula within 14 days of the procedure
• Patient receiving chemotherapy
• Patients with an immunodeficiency disease or condition
• Documented hypercoagulable state
• WBC < 2000/mm3
• Platelet count less than 100,000/mm3
• Chronic hepatitis or jaundice
• Simultaneous enrollment in another investigational device or drug study

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Englewood Hospital and Medical Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Kurt Wengerter, MD

Role: PRINCIPAL_INVESTIGATOR

Englewood Hospital and Medical Center

Locations

Englewood Hospital and Medical Center

Englewood, New Jersey, United States

Countries

United States

Other Identifiers

E-13-532

Identifier Type: -

Identifier Source: org_study_id