BONE ANCHORED PORT for Hemodialysis Treatment

Not Applicable

Terminated

• Conditions: End-Stage Renal Disease Requiring Haemodialysis; Hemodialysis Access Failure (Disorder)
• Interventions: Device: Bone Anchored Port System (BAP)

• Registration Number: NCT02069860
• Lead Sponsor: Cendres+Métaux

Brief Summary

A Bone Anchored Port System (BAP) will be implanted in the mastoid bone behind the ear, connected with a double lumen central venous catheter inserted in the jugular vein, and will be used in conjunction with an adapter as a permanent vascular access for hemodialysis treatment.

Detailed Description

STUDY OBJECTIVE The objective of the clinical investigation is to demonstrate feasibility regarding safety, efficiency and clinical performance of the BAP as a permanent access for chronic haemodialysis therapy in patients with renal failure to reach the certificate European (CE) mark and conduct a post market follow-up study.

PRIMARY ENDPOINT

1) Device survival probability after one year (product - limit estimator of Kaplan-Meier Analysis). An event is the primary failure of BAP, defined by necessity to remove the device: for any medical reason (e.g. infections at wound or mastoid, thrombosis, and severe patient discomfort)

SECONDARY ENDPOINTS

1. Performance - Implantation and primary healing process

* Failure to implant a device due to procedural complications or unforeseen anatomical reasons, except for intra-operatively detected exclusion criteria

* Successful attempt on the site contralateral to the planned side

* Duration of the implantation procedure measured from incision to final suture

* Duration of hospitalization before implantation / after implantation

* Time from implantation to first use for haemodialysis

* Rate of patients with complications stratified by

* Dura mater exposed / injured

* Blood sinus injured

* Injury of facial nerve

* Carotid artery puncture

* Central vein perforation

* Bleeding, defined as requirement for blood products

* Pneumothorax

* Hematothorax

* Initial healing and stabilization of BAP, Infections at implantation site

* Septicaemias with no other source of infection than surgical-procedures impairment for mechanical reasons

2. Performance - removal of catheter

* Failure to provide a blood flow ≥200ml/min for more than 2 consecutive weeks

* Catheter related and untreatable infection

* Surgical or interventional (Seldinger technique) procedure

* Persistent recirculation higher than 15%

3. Performance - Dialysis use

* Average blood flow rate

* Average venous pressure

* Average arterial pressure

* Recirculation

* Volume-corrected clearance (Kt/V)

* Access thrombosis reversible by non-surgical means

* Infections of any kind

* in anatomical structures around implant

* remote infections possibly related to the BAP

* bacteriemia/septicemia

4. Design Validation

* Questionnaire for the implantation surgeon

* Questionnaire for the dialysis staff

* Questionnaire for patients

* Quality of Life (QoL) Questionnaire (EQ-5D)

* Questionnaire for change / removal of catheter

Study Timeline

• Study First Submitted: 2013-12-11
• Study First Submitted QC: 2014-02-21
• Study First Posted: 2014-02-24
• Study Start: 2016-04-04
• Primary Completion: 2019-12-23
• Study Completion: 2022-07-12
• Status Verified: 2022-11
• Last Update Submitted: 2022-11-16
• Last Update Posted: 2022-11-21

Recruitment & Eligibility

• Status: TERMINATED
• Sex: All
• Target Recruitment: 6

Inclusion Criteria

• Indication for a permanent haemodialysis access
• Impossibility to construct or revise an AC-Fistula
• Age > 18 years.
• Written, informed consent.
• Availability of vascular imaging of the jugular vein at the implantation site with no contraindication for a jugular vein catheter

Exclusion Criteria

1. Clinical contraindications for the implantation of a BAP including:

   • known intolerance to any of the BAP materials

   • ongoing infections e.g.

     • mastoiditis / otitis media
     • skin infection in the area of presumed implantation-site
     • generalized acute and chronic infections

   • severe skin lesions (e.g. dermatitis, psoriasis) in the area of the presumed implantation site

   • previous surgery at the petrous bone

   • deafness

   • known significant bleeding disorder

   • known thrombophilia

2. Life expectancy less than 1 year from the time of enrolment in the study.

3. Expected transplantation within the intended study duration (i.e. known living donor).

4. Pregnancy or breast feeding.

5. Women of childbearing potential without appropriate contraceptive method.

6. Patient known to be HIV, hepatitis C or hepatitis B antigen positive.

7. Any form of substance abuse, psychiatric disorder or condition which, in the opinion of the investigator may complicate communication with the investigator.

8. Participation in another clinical study (medicinal, medical device) within the last 30 days.

9. Multiple participation of one subject in this clinical investigation.

10. Inability to understand German and to give written informed consent.

11. Patients suffering from epilepsy, addiction or other condition resulting in a higher risk of falling.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
Access for heamodialysis treatment	Bone Anchored Port System (BAP)	The Bone Anchored Port System (BAP) will be implanted in the mastoid bone behind the ear, connected with a double lumen central venous catheter inserted in the jugular vein, and will be used in conjunction with an adapter as a permanent vascular access for hemodialysis treatment

Primary Outcome Measures

Name	Time	Method
Device survival probability after one year	up to 12 months after Study start	An event is the primary failure of BAP, defined by necessity to remove the device for any medical reason (e.g. infections at wound or mastoid, thrombosis, and severe patient discomfort).

Secondary Outcome Measures

Name	Time	Method
Performance - Implantation and primary healing process	up to 18 months after Study start	Failure to implant a device due to procedural complications or unforeseen anatomical reasons, except for intra-operatively detected exclusion criteria; * Successful attempt on the site contralateral to the planned side; * Duration of the implantation procedure measured from incision to final suture; * Duration of hospitalization before implantation / after implantation; * Time from implantation to first use for haemodialysis; * Rate of patients with complications stratified by; * Dura mater exposed / injured; * Blood sinus injured; * Injury of facial nerve; * Carotid artery puncture; * Central vein perforation; * Bleeding, defined as requirement for blood products; * Pneumothorax; * Hematothorax; * Initial healing and stabilization of BAP, Infections at implantation site; * Septicaemias with no other source of infection than surgical-procedures impairment for mechanical reasons

Trial Locations

Locations (1)

Inselspital Bern; 🇨🇭 Bern, Switzerland