Arteriovenous Fistula Maturation FailureCAVONCT02632942
Criteria for Accessory Vein Obliteration Trial.
A study testing HAQ criteria and Current Recommendation in people with Arteriovenous Fistula Maturation Failure, run by King Faisal Specialist Hospital & Research Center at 1 site in Saudi Arabia.
Trial summary
Hemodialysis (HD) vascular access dysfunction is a huge clinical problem which results in significant morbidity amongst patients with End Stage Renal Disease (ESRD), causing a severe economic burden on any health care system. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Arteriovenous Fistula Maturation Failure
- What is being tested?
- HAQ criteria and Current Recommendation
- Type of treatment
- Surgery or procedure
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 50 participants
- Where
- 1 siteSaudi Arabia
- Study dates
- Sep 2015to Dec 2018
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- 1. All adult patients with age> 18 years and referred to KFSHRC for EFF satisfying any of the following criteria and willing to participate by providing informed consent will be included in the study:
- ESRD on dialysis with EFF at least 4 weeks post-surgery.
- Chronic kidney disease patients who are approaching ESRD with EFF and will need and are willing to start HD as soon as AVF matures.
Who cannot join
- Patients with AVF which is deeper than 0.8cm from the skin.
- AVF which is tortuous and lacks adequate straight segment for cannulation with 2 needles.
- Patients on anti-coagulation and those with bleeding or disorders.
- Life expectancy less than 12 months.
- Documented severe contrast allergy.
- Inability to come for timely and adequate follow up.
- Patients undergoing transplantation work up and expected to be transplanted within 6 months.
Trial locations and contacts
1 site in 1 country.
Saudi Arabia1 site, 1 recruiting
- Recruiting
King Faisal Specialist Hospital & Research Center
Riyadh, 11211
Naveed U Haq, MD, FASN, +966 11 4427492, nulhaq@kfshrc.edu.sa
Muhammad Azhar, MD, +966 11 4427492, mazhar@kfshrc.edu.sa
About this study
Official title: Assessing Clinical Utility of the Criteria for Accessory Vein Obliteration for Failing Arteriovenous Fistula.
Hemodialysis (HD) vascular access dysfunction is a huge clinical problem which results in significant morbidity amongst patients with End Stage Renal Disease (ESRD), causing a severe economic burden on any health care system. Native arteriovenous fistula (AVF) is the preferred form of permanent dialysis access since it is associated with the best long term outcome as compared to other forms of dialysis access. Despite the clinical benefits, many patients on HD do not have AVF as there dialysis access. One of the reasons for low AVF rates is early fistula failure (EFF). The two most important causes for EFF amenable to intervention are stenosis anywhere in the circuit and/or presence of accessory vein (av). Although management of stenosis is well established with relatively clear guidelines, the management of av lacks clear scientific approach. In a recent study researchers recommended a hemodialysis arteriovenous flow quantification-diameter (HAQ) criteria for accessory vein obliteration. The purpose of this controlled, blinded, prospective trial is to assess the clinical utility of the HAQ criteria as compared to current recommendations for av obliteration.
Read the detailed description
Hemodialysis (HD) vascular access dysfunction is a huge clinical problem which results in significant morbidity amongst patients with End Stage Renal Disease (ESRD), causing a severe economic burden on any health care system. Native arteriovenous fistula (AVF) is the preferred form of permanent dialysis access since it is associated with the best long term outcome as compared to other forms of dialysis access. Despite the clinical benefits, many patients on HD do not have AVF as there dialysis access. One of the reasons for low AVF rates is early fistula failure (EFF). EFF is defined as an AVF that never develops adequately for dialysis (failure to mature) or which fails within 3 months of starting dialysis. An adequate AVF for dialysis according to Dialysis Outcome Quality Initiative (DOQI) guidelines is the one which a) Has a flow of greater than 600ml/min, b) Has a diameter of 0.6cm or greater and c) Is approximately not deeper than 0.6cm from the skin surface. Between 23%-46% of newly constructed AVF have problems with early failure resulting in a dismal one year patency of 60-65%.
In order to devise a strategy to prevent EFF, one needs to understand the physiology of fistula maturation. Creation of an AVF leads to an immediate increase in flow through the vein due to the pressure gradient created. This increase in flow leads to increase wall shear stress which is defined mathematically by the formula 4ηQ/πr3, where η is blood viscosity, Q is blood flow and r is vessel radius. Shear stress thus is directly proportional to blood flow while inversely proportional to vessel diameter. After the creation of the AVF, the flow mediated increase in shear stress is mitigated by vessel dilatation through biological mediators. Consequently the shear stress is brought back to pre-anastomosis levels leading to vessel dilation. It seems that this positive remodeling of the vein leading to AVF maturation is dependent on increase in blood flow rather than the increase in pressure. Any pathology affecting the blood flow through the newly constructed AVF can thus lead to failure to mature.
The two most important causes for EFF amenable to intervention are stenosis anywhere in the circuit and/or presence of accessory veins. While stenosis development is pathological and accessory vein (av) presence is natural, both lead to decreased blood flow through the main AVF circuit, which may be responsible for failure to mature. Addressing these two entities in a timely fashion can lead to salvage of many AVF, which otherwise would have been abandoned. Although management of stenosis is well established with relatively clear guidelines, the management of av lacks clear scientific approach. It has been anecdotally recommended that any av with a diameter greater than 25% of the AVF diameter should be considered for ligation. It is also suggested that the significance of an av can be ascertained by assessing the flow of contrast through the av during an angiogram or by assessing the augmentation of AVF after manually occluding the av during the procedure. These current recommendations are very subjective and none have been adequately studied to date leading to considerable debate on the issue of when to obliterate an av. A scientific approach to obliteration of av is essential to avoid an unnecessary procedure, which may even be harmful. Also, obliterating a non-significant av and waiting for AVF to mature may cause a delay in making a definite decision for the patient. These patients may have other factors and not av as the cause of EFF. Conversely, not obliterating a significant av may also delay the use of AVF for dialysis by causing EFF. In a recent study researchers recommended a hemodialysis arteriovenous flow quantification-diameter (HAQ) criteria for accessory vein obliteration written below:
- 60% or greater diameter of the main AVF
- 50% diameter of AVF with at least one more av>40% in diameter.
- 50% in diameter and divides into branches of same size.
- av likely to interfere with cannulation on physical examination.
- >30% in diameter and associated with stenosis at site of origin.
The HAQ criteria for av obliteration is based on computational flow dynamic (CFD) models of AVF created using 2 dimensional CFD software. This criteria has not been tested in clinical trials and its clinical utility has not been established to date. The purpose of this controlled, blinded, prospective trial is to assess the clinical utility of the HAQ criteria as compared to current recommendations for av obliteration.
Specific Aim:
The purpose of this controlled, blinded, prospective trial is to assess the clinical utility of the HAQ criteria as compared to current recommendations for av obliteration.
Method and Materials:
Trial Design: The study will be a single center blinded, controlled and prospective trial. The study will be conducted according to the ethical standards of King Faisal Specialist Hospital \& Research Center (KFSHRC) for human experimentation and in compliance with the declaration of Helsinki.
Participants: The study will be conducted at the Interventional Nephrology section at KFSHRC, Riyadh, Saudi Arabia. All adult patients (Age>18 years) with End Stage Renal Disease (ESRD) or chronic kidney disease (CKD) with estimated glomerular filtration rate less than 10 approaching ESRD who have had an AVF created and has not matured enough to be used for dialysis 6 weeks after surgery will be eligible for consideration.
Design: All participants with EFF are currently evaluated for cause of EFF as the standard of practice at KFSHRC. Patients who agree to participate by providing informed consent will undergo the same routine evaluation for EFF. As mentioned before, stenosis anywhere in the AVF circuit and presence of av are the 2 most common causes for EFF. Patients in whom stenosis is the sole cause of EFF will be excluded from the study. Amongst eligible patients in whom av is the only cause of EFF will be directly undergo av obliteration. Before and after any av obliteration assessment of av will be done to ascertain whether it satisfies current recommendation or the HAQ criteria and to assess the effect of obliteration on access flows as shown in data collection sheet. Data on av will be interpreted by another expert, blinded to study details (other than the operator) after the procedure to assure accuracy. Those patients in which both av and stenosis are present will first undergo angioplasty of the stenotic region. These patients will be brought back at 4 weeks post intervention for re-assessment of AVF maturation by staff blinded to intervention details. av will be managed if indicated at that time. Patients who undergo av obliteration will be reassessed in 4 weeks for AVF maturation by staff blinded to intervention details. Patients who are thought to have mature AVF on clinical exam will be scheduled for cannulation. Final maturity will be defined as an AVF which undergoes 3 consecutive successful HD treatments using the AVF. Access flows will also be measured. The access flow studies using ultrasound dilution technique can be done on either of the first three treatment sessions. Ultrasound dilution technique is an accepted method for assessing access blood flows. Patients with mature AVF following interventions will be followed for 6 months with monthly evaluation with access flows and physical examination to assess primary and secondary patency. The follow up can be extended to another 18 months to assess long term patency but during that time access management and surveillance will be as per local center practice.
Procedural Details:
Angiograms under fluoroscopy will be performed as standard practice in such procedures. To assess arteriovenous anastamosis stenosis, arteriograms will be done rather than reflux angiogram which is more accurate in assessing av. As part of current guidelines for practice a puff of contrast is injected in the AVF and if there is av present it is assessed subjectively without any measurement and if it is thought to be significant it is ligated. But in this study the investigators will take measurements of the av as well as of the AVF which is the only additional step from the standard of care .In case of av presence, downstream sheath placement from the origin of av will be avoided as this may cause functional downstream stenosis leading to slightly high pressure in AVF causing alteration in the size and flow through the av. Data on the size of av and AVF diameter will be collected after adequate calibration of the system. This will be collected and sealed before any intervention and later interpreted by another expert in the field blinded to intervention to assure accuracy. This interpreter will assign whether the av satisfies the Standard or HAQ criteria.The investigators currently use a Phillips veradius fluoroscopy equipment. If the av qualifies for obliteration than obliteration will be performed. For obliteration of av either the surgical ligation or coil embolization will be used. Both are established current standards of practice. Successful obliteration will be defined as complete disappearance of av on repeat angiogram following the procedure. For details of data collected please see the data collection sheet at the end.
Statistical Design:
Sample Size:
For the purposes of designing this study in terms of sample size, the outcome variable of interest is whether the fistula matures or not, i.e. a binary outcome. The associated parameter is the so-called binomial parameter and is denoted here as π. The predictor variable is whether the patient meets the HAQ criteria or not, i.e. also a binary variable. The notation for this variable will be X, and that will take on the value one if the patient meets the HAQ criteria and the value zero if the patient does not meet the HAQ criteria. Given this notation, then π will be further defined as π0 for those patients that do not meet the criteria, and π1 for those who do.
In statistical terms, the research hypothesis is H0: π1 - π0 = 0 vs H1: π1 - π0>= δ> 0. Of clinical interest is to conclude H1 if δ is at least equal to 0.20, i.e. that the probability that the fistula will mature is at least 20% greater for those meeting the HAQ criteria than for those not meeting it.
With the research hypothesis framed as such, then the sample size calculation becomes one of estimating a binomial parameter, i.e.
n = 4(1-πi)πi/M squared, where here M equals 0.05. For varying values of πi, n is maximized for πi equal to 0.5. At such a maximum, then n equals 25, i.e. 25 patients would be required of each type (those meeting and those not meeting the HAQ criteria).
Statistical Analysis According to the above description of the statistical design of the project, the analyses will involve a test between two binomial proportions. Fisher's Exact test would be carried out and with a size α = 0.05. Additional analyses will also be carried out to investigate the exact relationship between the size of the accessory vein and the probability of the fistula maturing. This would be a logistic regression analysis with repeated covariates and will be analyzed with generalized estimating equations (GEE).
- Conditions
- Arteriovenous Fistula Maturation Failure
- Being tested
- HAQ criteria, Current Recommendation
- Keywords
- arteriovenous fistula, hemodialysis, maturation
- Medical subject headings
- Arteriovenous Fistula
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
HAQ criteriaProcedure or surgery
Also called HAQ criteria based obliteration
Obliteration of accessory vein which satisfy the HAQ criteria as below:
- 60% or greater diameter of the main AVF
- 50% diameter of AVF with at least one more av>40% in diameter.
- 50% in diameter and divides into branches of same size.
- av likely to interfere with cannulation on physical examination.
- >30% in diameter and associated with stenosis at site of origin.
Current RecommendationProcedure or surgery
Also called Current recommendation based accessory vein obliteration
Obliteration of accessory vein which satisfy current recommendations defined as the diameter greater than 25% of the AVF diameter.
| Study group | Role | What they receive |
|---|---|---|
| HAQ Criteria | Experimental | Obliteration of accessory vein which satisfy the HAQ criteria as below:
1. 60% or greater diameter of the main AVF
2. 50% diameter of AVF with at least one more av>40% in diameter.
3. 50% in diameter and divides into branches of same size.
4. av likely to interfere with cannulation on physical examination.
5. >30% in diameter and associated with stenosis at site of origin. Receives: Procedure: HAQ criteria |
| Current Recommendation | Active comparator | Obliteration of accessory vein which satisfy the current recommendations only defined as accessory vein with a diameter greater than 25% of the AVF diameter. Receives: Procedure: Current Recommendation |
What is being measured
The primary outcome is the main question the study is designed to answer.
Maturation of AVF
Maturation of AVF defined as an AVF which is used for hemodialysis with a pump speed of at least 300ml/min for 3 consecutive treatments
Measured: 3 months
Secondary outcomes (2)
Primary Patency
AVF which is still being used for hemodialysis with a pump speed of at least 300 ml/min without any additional procedures.
Measured: 6 months
Secondary Patency
AVF which is still being used for hemodialysis with a pump speed of at least 300 ml/min with help of additional procedures.
Measured: 6 months
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted17 Dec 2015 (estimated)
- Study startSep 2015
- Primary completionSep 2018 (estimated)
- Study completionDec 2018 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (9)Papers the sponsor has linked to this study.
- Other trials for Arteriovenous Fistula Maturation FailureStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- Double blind
- Who is masked
- Participant, Outcomes assessor
- Enrolment
- 50 participants (estimated)
Sponsor and investigators
- Lead sponsor
- King Faisal Specialist Hospital & Research Center
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Naveed Ul Haq, King Faisal Specialist Hospital & Research Center
- Investigators
- Naveed Haq, MD, FASN, Principal investigator, King Faisal Specialist Hospital & Research Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02632942
- Sponsor's protocol ID
- 2141 125
- Acronym
- CAVO
- Status last verified
- Oct 2016
- First submitted
- 15 Dec 2015
- Last updated
- 4 Oct 2016
- Results posted
- No
- Data monitoring committee
- No
Publications
Feldman HI, Kobrin S, Wasserstein A. Hemodialysis vascular access morbidity. J Am Soc Nephrol. 1996 Apr;7(4):523-35. doi: 10.1681/ASN.V74523.
PubMed 8724885Beathard GA, Arnold P, Jackson J, Litchfield T; Physician Operators Forum of RMS Lifeline. Aggressive treatment of early fistula failure. Kidney Int. 2003 Oct;64(4):1487-94. doi: 10.1046/j.1523-1755.2003.00210.x.
PubMed 12969170Vascular Access 2006 Work Group. Clinical practice guidelines for vascular access. Am J Kidney Dis. 2006 Jul;48 Suppl 1:S176-247. doi: 10.1053/j.ajkd.2006.04.029. No abstract available.
PubMed 16813989Roy-Chaudhury P, Spergel LM, Besarab A, Asif A, Ravani P. Biology of arteriovenous fistula failure. J Nephrol. 2007 Mar-Apr;20(2):150-63.
PubMed 17514619Beathard GA, Settle SM, Shields MW. Salvage of the nonfunctioning arteriovenous fistula. Am J Kidney Dis. 1999 May;33(5):910-6. doi: 10.1016/s0272-6386(99)70425-7.
PubMed 10213648Nassar GM, Nguyen B, Rhee E, Achkar K. Endovascular treatment of the "failing to mature" arteriovenous fistula. Clin J Am Soc Nephrol. 2006 Mar;1(2):275-80. doi: 10.2215/CJN.00360705. Epub 2006 Jan 4.
PubMed 17699217Faiyaz R, Abreo K, Zaman F, Pervez A, Zibari G, Work J. Salvage of poorly developed arteriovenous fistulae with percutaneous ligation of accessory veins. Am J Kidney Dis. 2002 Apr;39(4):824-7. doi: 10.1053/ajkd.2002.32003.
PubMed 11920349Haq NU, Albaqumi M. Accessory vein obliteration criteria for immature fistulae: a modest proposal for an old paradigm. Semin Dial. 2014 Sep-Oct;27(5):E51-4. doi: 10.1111/sdi.12239. Epub 2014 May 6.
PubMed 24796386Haq NU, Althaf MM, Lee T. Accessory Vein Obliteration for Early Fistula Failure: A Myth or Reality? Adv Chronic Kidney Dis. 2015 Nov;22(6):438-45. doi: 10.1053/j.ackd.2015.08.001.
PubMed 26524948
Study at a glance
From the registry record, last updated by the sponsor on 4 Oct 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Assessing Clinical Utility of the Criteria for Accessory Vein Obliteration for Failing Arteriovenous Fistula.
- ClinicalTrials.gov ID
- NCT02632942
- Acronym / sponsor ID
- CAVO / 2141 125
- Conditions
- Arteriovenous Fistula Maturation Failure
- Keywords
- arteriovenous fistula, hemodialysis, maturation
- Study type
- Interventional
- Recruitment status
- Unknown status
- Enrolment
- 50 participants (estimated)
- Lead sponsor
- King Faisal Specialist Hospital & Research CenterUniversity, hospital or other
- Study start
- Sep 2015
- Primary completion
- Sep 2018 (estimated)
- Study completion
- Dec 2018 (estimated)
- First posted
- 17 Dec 2015 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Hemodialysis (HD) vascular access dysfunction is a huge clinical problem which results in significant morbidity amongst patients with End Stage Renal Disease (ESRD), causing a severe economic burden on any health care system. Native arteriovenous fistula (AVF) is the preferred form of permanent dialysis access since it is associated with the best long term outcome as compared to other forms of dialysis access. Despite the clinical benefits, many patients on HD do not have AVF as there dialysis access. One of the reasons for low AVF rates is early fistula failure (EFF). The two most important causes for EFF amenable to intervention are stenosis anywhere in the circuit and/or presence of accessory vein (av). Although management of stenosis is well established with relatively clear guidelines, the management of av lacks clear scientific approach. In a recent study researchers recommended a hemodialysis arteriovenous flow quantification-diameter (HAQ) criteria for accessory vein obliteration. The purpose of this controlled, blinded, prospective trial is to assess the clinical utility of the HAQ criteria as compared to current recommendations for av obliteration.
Detailed description
Hemodialysis (HD) vascular access dysfunction is a huge clinical problem which results in significant morbidity amongst patients with End Stage Renal Disease (ESRD), causing a severe economic burden on any health care system. Native arteriovenous fistula (AVF) is the preferred form of permanent dialysis access since it is associated with the best long term outcome as compared to other forms of dialysis access. Despite the clinical benefits, many patients on HD do not have AVF as there dialysis access. One of the reasons for low AVF rates is early fistula failure (EFF). EFF is defined as an AVF that never develops adequately for dialysis (failure to mature) or which fails within 3 months of starting dialysis. An adequate AVF for dialysis according to Dialysis Outcome Quality Initiative (DOQI) guidelines is the one which a) Has a flow of greater than 600ml/min, b) Has a diameter of 0.6cm or greater and c) Is approximately not deeper than 0.6cm from the skin surface. Between 23%-46% of newly constructed AVF have problems with early failure resulting in a dismal one year patency of 60-65%.
In order to devise a strategy to prevent EFF, one needs to understand the physiology of fistula maturation. Creation of an AVF leads to an immediate increase in flow through the vein due to the pressure gradient created. This increase in flow leads to increase wall shear stress which is defined mathematically by the formula 4ηQ/πr3, where η is blood viscosity, Q is blood flow and r is vessel radius. Shear stress thus is directly proportional to blood flow while inversely proportional to vessel diameter. After the creation of the AVF, the flow mediated increase in shear stress is mitigated by vessel dilatation through biological mediators. Consequently the shear stress is brought back to pre-anastomosis levels leading to vessel dilation. It seems that this positive remodeling of the vein leading to AVF maturation is dependent on increase in blood flow rather than the increase in pressure. Any pathology affecting the blood flow through the newly constructed AVF can thus lead to failure to mature.
The two most important causes for EFF amenable to intervention are stenosis anywhere in the circuit and/or presence of accessory veins. While stenosis development is pathological and accessory vein (av) presence is natural, both lead to decreased blood flow through the main AVF circuit, which may be responsible for failure to mature. Addressing these two entities in a timely fashion can lead to salvage of many AVF, which otherwise would have been abandoned. Although management of stenosis is well established with relatively clear guidelines, the management of av lacks clear scientific approach. It has been anecdotally recommended that any av with a diameter greater than 25% of the AVF diameter should be considered for ligation. It is also suggested that the significance of an av can be ascertained by assessing the flow of contrast through the av during an angiogram or by assessing the augmentation of AVF after manually occluding the av during the procedure. These current recommendations are very subjective and none have been adequately studied to date leading to considerable debate on the issue of when to obliterate an av. A scientific approach to obliteration of av is essential to avoid an unnecessary procedure, which may even be harmful. Also, obliterating a non-significant av and waiting for AVF to mature may cause a delay in making a definite decision for the patient. These patients may have other factors and not av as the cause of EFF. Conversely, not obliterating a significant av may also delay the use of AVF for dialysis by causing EFF. In a recent study researchers recommended a hemodialysis arteriovenous flow quantification-diameter (HAQ) criteria for accessory vein obliteration written below:
- 60% or greater diameter of the main AVF
- 50% diameter of AVF with at least one more av>40% in diameter.
- 50% in diameter and divides into branches of same size.
- av likely to interfere with cannulation on physical examination.
- >30% in diameter and associated with stenosis at site of origin.
The HAQ criteria for av obliteration is based on computational flow dynamic (CFD) models of AVF created using 2 dimensional CFD software. This criteria has not been tested in clinical trials and its clinical utility has not been established to date. The purpose of this controlled, blinded, prospective trial is to assess the clinical utility of the HAQ criteria as compared to current recommendations for av obliteration.
Specific Aim:
The purpose of this controlled, blinded, prospective trial is to assess the clinical utility of the HAQ criteria as compared to current recommendations for av obliteration.
Method and Materials:
Trial Design: The study will be a single center blinded, controlled and prospective trial. The study will be conducted according to the ethical standards of King Faisal Specialist Hospital \& Research Center (KFSHRC) for human experimentation and in compliance with the declaration of Helsinki.
Participants: The study will be conducted at the Interventional Nephrology section at KFSHRC, Riyadh, Saudi Arabia. All adult patients (Age>18 years) with End Stage Renal Disease (ESRD) or chronic kidney disease (CKD) with estimated glomerular filtration rate less than 10 approaching ESRD who have had an AVF created and has not matured enough to be used for dialysis 6 weeks after surgery will be eligible for consideration.
Design: All participants with EFF are currently evaluated for cause of EFF as the standard of practice at KFSHRC. Patients who agree to participate by providing informed consent will undergo the same routine evaluation for EFF. As mentioned before, stenosis anywhere in the AVF circuit and presence of av are the 2 most common causes for EFF. Patients in whom stenosis is the sole cause of EFF will be excluded from the study. Amongst eligible patients in whom av is the only cause of EFF will be directly undergo av obliteration. Before and after any av obliteration assessment of av will be done to ascertain whether it satisfies current recommendation or the HAQ criteria and to assess the effect of obliteration on access flows as shown in data collection sheet. Data on av will be interpreted by another expert, blinded to study details (other than the operator) after the procedure to assure accuracy. Those patients in which both av and stenosis are present will first undergo angioplasty of the stenotic region. These patients will be brought back at 4 weeks post intervention for re-assessment of AVF maturation by staff blinded to intervention details. av will be managed if indicated at that time. Patients who undergo av obliteration will be reassessed in 4 weeks for AVF maturation by staff blinded to intervention details. Patients who are thought to have mature AVF on clinical exam will be scheduled for cannulation. Final maturity will be defined as an AVF which undergoes 3 consecutive successful HD treatments using the AVF. Access flows will also be measured. The access flow studies using ultrasound dilution technique can be done on either of the first three treatment sessions. Ultrasound dilution technique is an accepted method for assessing access blood flows. Patients with mature AVF following interventions will be followed for 6 months with monthly evaluation with access flows and physical examination to assess primary and secondary patency. The follow up can be extended to another 18 months to assess long term patency but during that time access management and surveillance will be as per local center practice.
Procedural Details:
Angiograms under fluoroscopy will be performed as standard practice in such procedures. To assess arteriovenous anastamosis stenosis, arteriograms will be done rather than reflux angiogram which is more accurate in assessing av. As part of current guidelines for practice a puff of contrast is injected in the AVF and if there is av present it is assessed subjectively without any measurement and if it is thought to be significant it is ligated. But in this study the investigators will take measurements of the av as well as of the AVF which is the only additional step from the standard of care .In case of av presence, downstream sheath placement from the origin of av will be avoided as this may cause functional downstream stenosis leading to slightly high pressure in AVF causing alteration in the size and flow through the av. Data on the size of av and AVF diameter will be collected after adequate calibration of the system. This will be collected and sealed before any intervention and later interpreted by another expert in the field blinded to intervention to assure accuracy. This interpreter will assign whether the av satisfies the Standard or HAQ criteria.The investigators currently use a Phillips veradius fluoroscopy equipment. If the av qualifies for obliteration than obliteration will be performed. For obliteration of av either the surgical ligation or coil embolization will be used. Both are established current standards of practice. Successful obliteration will be defined as complete disappearance of av on repeat angiogram following the procedure. For details of data collected please see the data collection sheet at the end.
Statistical Design:
Sample Size:
For the purposes of designing this study in terms of sample size, the outcome variable of interest is whether the fistula matures or not, i.e. a binary outcome. The associated parameter is the so-called binomial parameter and is denoted here as π. The predictor variable is whether the patient meets the HAQ criteria or not, i.e. also a binary variable. The notation for this variable will be X, and that will take on the value one if the patient meets the HAQ criteria and the value zero if the patient does not meet the HAQ criteria. Given this notation, then π will be further defined as π0 for those patients that do not meet the criteria, and π1 for those who do.
In statistical terms, the research hypothesis is H0: π1 - π0 = 0 vs H1: π1 - π0>= δ> 0. Of clinical interest is to conclude H1 if δ is at least equal to 0.20, i.e. that the probability that the fistula will mature is at least 20% greater for those meeting the HAQ criteria than for those not meeting it.
With the research hypothesis framed as such, then the sample size calculation becomes one of estimating a binomial parameter, i.e.
n = 4(1-πi)πi/M squared, where here M equals 0.05. For varying values of πi, n is maximized for πi equal to 0.5. At such a maximum, then n equals 25, i.e. 25 patients would be required of each type (those meeting and those not meeting the HAQ criteria).
Statistical Analysis According to the above description of the statistical design of the project, the analyses will involve a test between two binomial proportions. Fisher's Exact test would be carried out and with a size α = 0.05. Additional analyses will also be carried out to investigate the exact relationship between the size of the accessory vein and the probability of the fistula maturing. This would be a logistic regression analysis with repeated covariates and will be analyzed with generalized estimating equations (GEE).
Study design
- Primary purpose
- Treatment
- Allocation
- Non-randomised
- Intervention model
- Parallel groups
- Masking
- Double blind (participant, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| HAQ Criteria | Experimental | Procedure: HAQ criteriaObliteration of accessory vein which satisfy the HAQ criteria as below: 1. 60% or greater diameter of the main AVF 2. 50% diameter of AVF with at least one more av>40% in diameter. 3. 50% in diameter and divides into branches of same size. 4. av likely to interfere with cannulation on physical examination. 5. >30% in diameter and associated with stenosis at site of origin. |
| Current Recommendation | Active comparator | Procedure: Current RecommendationObliteration of accessory vein which satisfy the current recommendations only defined as accessory vein with a diameter greater than 25% of the AVF diameter. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (3 listed)
- 1. All adult patients with age> 18 years and referred to KFSHRC for EFF satisfying any of the following criteria and willing to participate by providing informed consent will be included in the study:
- ESRD on dialysis with EFF at least 4 weeks post-surgery.
- Chronic kidney disease patients who are approaching ESRD with EFF and will need and are willing to start HD as soon as AVF matures.
Key exclusion criteria (7 listed)
- Patients with AVF which is deeper than 0.8cm from the skin.
- AVF which is tortuous and lacks adequate straight segment for cannulation with 2 needles.
- Patients on anti-coagulation and those with bleeding or disorders.
- Life expectancy less than 12 months.
- Documented severe contrast allergy.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| HAQ criteriaAlso: HAQ criteria based obliterationObliteration of accessory vein which satisfy the HAQ criteria as below: 1. 60% or greater diameter of the main AVF 2. 50% diameter of AVF with at least one more av>40% in diameter. 3. 50% in diameter and divides into branches of same size. 4. av likely to interfere with cannulation on physical examination. 5. >30% in diameter and associated with stenosis at site of origin. | Procedure or surgery | HAQ Criteria |
| Current RecommendationAlso: Current recommendation based accessory vein obliterationObliteration of accessory vein which satisfy current recommendations defined as the diameter greater than 25% of the AVF diameter. | Procedure or surgery | Current Recommendation |
Primary outcome
Maturation of AVF
Time frame: 3 months
Maturation of AVF defined as an AVF which is used for hemodialysis with a pump speed of at least 300ml/min for 3 consecutive treatments
2 secondary outcomes
Primary Patency
Time frame: 6 months
Secondary Patency
Time frame: 6 months
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 4 Oct 2016.
- Background: PubMed 8724885Feldman HI, Kobrin S, Wasserstein A. Hemodialysis vascular access morbidity. J Am Soc Nephrol. 1996 Apr;7(4):523-35. doi: 10.1681/ASN.V74523.
- Background: PubMed 12969170Beathard GA, Arnold P, Jackson J, Litchfield T; Physician Operators Forum of RMS Lifeline. Aggressive treatment of early fistula failure. Kidney Int. 2003 Oct;64(4):1487-94. doi: 10.1046/j.1523-1755.2003.00210.x.
- Background: PubMed 16813989Vascular Access 2006 Work Group. Clinical practice guidelines for vascular access. Am J Kidney Dis. 2006 Jul;48 Suppl 1:S176-247. doi: 10.1053/j.ajkd.2006.04.029. No abstract available.
- Background: PubMed 17514619Roy-Chaudhury P, Spergel LM, Besarab A, Asif A, Ravani P. Biology of arteriovenous fistula failure. J Nephrol. 2007 Mar-Apr;20(2):150-63.
- Background: PubMed 10213648Beathard GA, Settle SM, Shields MW. Salvage of the nonfunctioning arteriovenous fistula. Am J Kidney Dis. 1999 May;33(5):910-6. doi: 10.1016/s0272-6386(99)70425-7.
- Background: PubMed 17699217Nassar GM, Nguyen B, Rhee E, Achkar K. Endovascular treatment of the "failing to mature" arteriovenous fistula. Clin J Am Soc Nephrol. 2006 Mar;1(2):275-80. doi: 10.2215/CJN.00360705. Epub 2006 Jan 4.
- Background: PubMed 11920349Faiyaz R, Abreo K, Zaman F, Pervez A, Zibari G, Work J. Salvage of poorly developed arteriovenous fistulae with percutaneous ligation of accessory veins. Am J Kidney Dis. 2002 Apr;39(4):824-7. doi: 10.1053/ajkd.2002.32003.
- Background: PubMed 24796386Haq NU, Albaqumi M. Accessory vein obliteration criteria for immature fistulae: a modest proposal for an old paradigm. Semin Dial. 2014 Sep-Oct;27(5):E51-4. doi: 10.1111/sdi.12239. Epub 2014 May 6.
- Background: PubMed 26524948Haq NU, Althaf MM, Lee T. Accessory Vein Obliteration for Early Fistula Failure: A Myth or Reality? Adv Chronic Kidney Dis. 2015 Nov;22(6):438-45. doi: 10.1053/j.ackd.2015.08.001.
Related trials for Arteriovenous Fistula Maturation Failure
Active, not recruitingObservational study
Clinical and Mechanistic Research on Autogenous Arteriovenous Fistula in Hemodialysis Patients
Arteriovenous Fistula Maturation Failure in End-stage Renal Disease
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Naveed Haq, MD, FASN principal investigator
King Faisal Specialist Hospital & Research Center
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing HAQ criteria and Current Recommendation in people with Arteriovenous Fistula Maturation Failure, run by King Faisal Specialist Hospital & Research Center at 1 site in Saudi Arabia.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 3 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 4 Oct 2016. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in Saudi Arabia. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Naveed U Haq, MD, FASN (+966 11 4427492, nulhaq@kfshrc.edu.sa), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Maturation of AVF (time frame: 3 months). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02632942, which also lists 9 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Oct 2016; AzTrials last refreshed its copy on 6 Nov 2026.