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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT03764358
Other study ID # AUSTRIA
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date March 6, 2019
Est. completion date October 4, 2022

Study information

Verified date December 2018
Source Medical University of Vienna
Contact Benjamin Schairer, MD
Phone 0043 40400 43890
Email benjamin.schairer@meduniwien.ac.at
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Patients with diagnosed end stage renal disease and indication for chronic dialysis rely on a well-functioning access for dialysis. The KDOQI Guidelines For Vascular Access follows a "fistula first" approach for every patient, whenever possible. Thus, every patient, regardless of age, clinical state and co-morbidities an arteriovenous fistula should be preferred over a tunneled cuffed catheter (TCC). These recommendations are based on retrospective and register studies. There have been no prospective studies in this subject so far. In addition, most of the collected data refers to patients of all ages, regardless of their comorbidities and general clinical state. In this study, we address differences between two dialysis vascular access types in elderly or frail patients. We will compare TCCs with arteriovenous fistulas in the selected population consisting of elderly patients over 60 years of age or those with a Charlson Comorbidity Index >6 independent of age. In our hypothesis TCCs will be superior to arteriovenous fistulas in this population regarding the examined end-points.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 220
Est. completion date October 4, 2022
Est. primary completion date April 4, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria:

- Age of 60 and higher

- CCI Score >6 when under 60 years

- Patients with CKD G5 A1-3 with indication for hemodialysis

- Stable clinical condition

- Eligibility for both arteriovenous fistula on the upper extremitiesandTCC

- Availability for follow-up.

- Written informed consent.

Exclusion Criteria:

- Uncontrolled infection at screening and/or CRP >5 mg/dl (normal <0.5 mg/dl) at screening.

- Poor general condition of health or malignancy not in remission at screening

- Major surgery within 12 weeks before screening.

- Pre-existent vascular access.

- Patient not eligible for any one of the vascular access options.

Study Design


Intervention

Device:
Arteriovenous Fistula
Surgical implantation of an arteriovenous fistula for hemodialysis
Tunneled Cuffed Catheter
Placement of a tunneled cuffed catheter in surgical theatre

Locations

Country Name City State
Austria Department of Medicine III, Devision of Nephrology and Dialysis, Medical University of Vienna Vienna

Sponsors (1)

Lead Sponsor Collaborator
Medical University of Vienna

Country where clinical trial is conducted

Austria, 

Outcome

Type Measure Description Time frame Safety issue
Primary Composite primary end-point of any access related complication Loss of access, catheter related bloodstream infection/shunt infection and/or thrombosis From placement of vascular access through study completion, an average of 3 years.
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