Efficacy and Local Tolerability of Topically Applied Heparin on the Suitability of Newly Constructed Primary Arteriovenous Fistulas in Patients Planned for Haemodialysis

Cyathus Exquirere Pharmaforschung

Status and phase

Terminated

Phase 2

Conditions

Haemodialysis

Treatments

Drug: Placebo Cutaneous Spray

Drug: Heparin 2,400 IU /ml Cutaneous Spray

Study type

Interventional

Funder types

Industry

Identifiers

NCT01382888

CYT/Heparin - 01/11

2011-000455-16 (EudraCT Number)

Details and patient eligibility

About

The primary objective of this study is to evaluate the effect of topically applied heparin in comparison to placebo on suitability of newly constructed primary arteriovenous fistulas in patients planned for haemodialysis at 7th week (± 1 week) after first study drug administration.

Full description

The clinical dilemma surrounding the maturation and suitability of the AVF in patients undergoing hemodialysis suggests the requirement for a medication that can be added to the standard therapy with in order to help maturation and suitability of newly created AVF. Numerous research papers published over the past 25 years indicate that heparin might have a positive impact on main factors involved in the early failure of native AVF to mature.

In total 56 eligible patients will be enrolled after giving informed consent. Screening will take place in the preceding 6 weeks before scheduled AVF creation. Only patients receiving a Brescia - Cimino (radio - cephalic) fistula or a distal ulnar artery to basilica vein, proximal radial artery to transposed basilica vein, brachial artery to transposed basilica vein and brachial artery to cephalic vein will later be randomized. Patients will be randomly assigned in equal proportions (each group 28 patients) to receive either topically applied heparin (Heparin 2,400 IU /ml Cutaneous Spray) or placebo using a computer-generated randomization. Participants and members of the study team will be blinded to treatment assignment. Patients will be instructed how to use and administer study medication for the consecutive 24 weeks following randomization.

Assessment of the primary endpoint (suitability of newly constructed primary arteriovenous fistulas) is done at 7th week (± 1 week) after first study drug administration. The suitability and unassisted patency and local safety and tolerability by physician and patient of the AVF will also be determined at 12 weeks (± 1 week) and 24 weeks (± 1 week) after first study drug administration. Administration of study medication will be stopped at week 24 after randomization.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Male and/or female outpatients
Aged over 18 years
Stage 4 or 5 Chronic kidney Disease according to KDOQI classification
Surgery to create an arteriovenous fistula in the lower arm is planned
If female of childbearing potential: agree to maintain reliable birth control throughout the study and negative (urine) pregnancy test

Exclusion criteria

Known hypersensitivity to any component of the study medication
History of previous arm (side of planned AVF), neck, or chest surgery/trauma
Anticipated kidney transplant from living donor within the next 3 months
Presence of any comorbidity that limits patient's life expectancy to less than 6 months.
Pregnancy / lactation or intention to fall pregnant during the time course of the study and women of childbearing potential who are not using adequate contraception
Known bleeding disorder or established diagnosis of active or suspected bleeding
Platelet count less than 80 x 10^9/L
Uncontrolled hypertension: Diastolic blood pressure > 115 mm Hg or Systolic blood pressure > 200 mm Hg