Study on Fistuloplasty Using Flow Measurement Guidance

This study is currently recruiting participants.
Verified October 2012 by McGill University Health Center
Sponsor:
Information provided by (Responsible Party):
McGill University Health Center
ClinicalTrials.gov Identifier:
NCT01643733
First received: July 10, 2012
Last updated: October 18, 2012
Last verified: October 2012

July 10, 2012
October 18, 2012
October 2012
February 2013   (final data collection date for primary outcome measure)
Time to reintervention [ Time Frame: 6 months ] [ Designated as safety issue: No ]
Time between intervention and the need for repeat intervention (based on standard dialysis screening systems).
Same as current
Complete list of historical versions of study NCT01643733 on ClinicalTrials.gov Archive Site
  • Effect of treatment on rate of change in Transonics flow measurements [ Time Frame: Baseline, 2 weeks, one, two three and 6 months ] [ Designated as safety issue: No ]
    Analysis of Transonics flow measurements obtained post intervention during the follow-up of six months
  • Change in dialysis efficiency post treatment [ Time Frame: One month, 2, 3 and six months ] [ Designated as safety issue: No ]
    Comparison of Dialysis efficiency scores pre and post treatment
  • Significance of stenoses as detected by Transonics, compared with angiography [ Time Frame: 1 day, ie.will be asessed immediately following intial intervention only. ] [ Designated as safety issue: No ]
    Assessment of extent to which using flow measurements can improve ability to detect hemodynamically significant stenoses.
  • Nature of Procedure using Transonics versus Angiographic assessment [ Time Frame: Six months ] [ Designated as safety issue: No ]
    Comparison of procedures carried out between the group where Transonics flow measurements are used to guide intervention, versus the group where angiographic assessment is used.
Same as current
Not Provided
Not Provided
 
Study on Fistuloplasty Using Flow Measurement Guidance
Confirmation of Clinical Effectiveness and Safety of Use of Transonics in Determining Success of Intervention in Dialysis Fistulae

Hypothesis: The primary objective of this study is to assess whether using a flow measurement device, in this case the Transonics flow device, as an end-point to interventional treatment of diseased dialysis fistulae can help increase immediate treatment success in terms of quality of dialysis immediately following the treatment and increasing time to reintervention.

This is a prospective randomized study. All intervention will be carried out by experienced radiologists in the two study centres.

At least fifty (50) consecutive subjects meeting the eligibility criteria, scheduled for angiographic assessment (with a view to PTA if necessary), will be invited to participate in the study. Subjects who consent will undergo their procedure, which will be performed by a qualified interventional radiology doctor (IRD). Patients will be randomly allocated to each group. All previous Transonics measurements will be available to the treating IRD. A target flow rate will be pre-decided in all patients in consultation with the nephrology service.

  • All patients will undergo a fistulogram, a routine interventional Xray exam where radiocontrast media (RCM) is injected under X ray control to identify narrowings within the vessels. Significant lesions will be identified based on this exam. If a lesion is believed to be significant, the patient will be assigned to either arm of the study. The details of the disease present will be recorded as location and percentage stenosis.
  • In the control arm, an initial Transonic measurement pre-treatment will be performed. The interventionalist will select the most significant lesion based on angiographic appearances and treat this lesion, which may require use of multiple balloons for the same lesion. At this point a Transonics measurement will be taken - Measurement A. The results will not be revealed to the interventionalist, who will proceed with the procedure as per their standard practice. A Transonics measurement will be taken after treatment of each of the significant lesions identified at the start of the exam. A post-procedural Transonics measurement (Measurement X) will also be taken, again the interventionalist will blinded as to this result. The appearances on completion angiography will be recorded as percentage stenosis remaining.
  • In the Transonics arm, a pre-treatment Transonic measurement will be done. The lesions will be treated. Once Measurement A is obtained, the interventionalist will only be informed if the target value has been reached or not, they will not be told the actual value. This will be repeated for the treatment of each subsequent lesion, with the interventionalist being informed if the target had been reached, whilst being blinded as to the Transonics result, until the target has been achieved. The interventionalist will not pursue further treatment, regardless of the Transonics measurement, if he deems it would pose a greater risk of complication to the patient, than his/her standard practice. The appearances on completion angiography will be recorded as percentage stenosis remaining.
Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Double Blind (Investigator, Outcomes Assessor)
Primary Purpose: Treatment
  • Renal Dialysis
  • Renal Failure
Device: Using Flow measurements to guide fistula angioplasty (Transonics)
Transonics flow measurements in the fistula would be used to guide the fistula intervention
  • Experimental: Transonics Arm
    Intervention will be guided by flow through the fistula as guided by Transonics flow measurements
    Intervention: Device: Using Flow measurements to guide fistula angioplasty (Transonics)
  • No Intervention: Control arm
    Patient will undergo normal fistula intervention guided only by angiographic assessment
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
50
March 2013
February 2013   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Male or non-pregnant female subjects, between the ages of 18 and 80 at the time of enrollment.
  • Subjects referred to us from the Dialysis units located in the study centres for clinically indicated fistulogram and fistula treatment.
  • Written informed consent to participate in the study.
  • Ability to comply with the requirements of the study procedures

Exclusion Criteria:

  • Significant coagulopathy that cannot be adequately corrected.
  • Subjects who participated in an active stage of any drug, intervention or treatment trial within 30 days of enrollment.
  • Subjects with preexisting conditions, which, in the opinion of the investigator, interfere with the conduct of the study. Patients will only be excluded on this basis following discussion with another interventional radiologist and the referring nephrologist.
  • Subjects who are uncooperative or cannot follow instructions.
  • Mental state that may preclude completion of the study procedure or ability to obtain informed consent.
  • Pregnant or nursing female subjects.
  • Patients whose fistulae have never become functional.
  • Patients with PTFE grafts/non-native fistulae
  • Patients who have had previous stenting of fistulae
Both
16 Years to 90 Years
No
Contact: Richard Lindsay, MB Bch BaO 5149341934 rwklindsay@hotmail.com
Canada
 
NCT01643733
12-133-SDR
Yes
McGill University Health Center
McGill University Health Center
Not Provided
Principal Investigator: David Valenti, MD McGill University Health Center
Principal Investigator: Louis Boucher, MD McGill University Health Center
McGill University Health Center
October 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP