Hemodialysis Access FailureNCT04692636
BP Variability on the Outcomes of Hemodialysis Vascular Access
An observational study of Hemodialysis Access Failure and Blood Pressure, run by National Taiwan University Hospital Hsin-Chu Branch at 1 site in Taiwan.
Trial summary
Hemodialysis vascular access dysfunction continues to be a major source of morbidity and mortality in patients with ESRD. Thrombosis is the most common cause of secondary vascular access failure Although intimal hyperplasia at the outflow vein is the most common cause of thrombosis, 20-40% of thrombosis may develop… Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Hemodialysis Access Failure, Blood Pressure, Dialysis Access Malfunction
- What is being tested?
- Measure: BP measurements, inter-dialysis BP variability, intra-dialysis hypotension
- How many people
- 1,300 participants
- Where
- 1 siteTaiwan
- Study dates
- 1 Jan 2018to 31 Dec 2022
- How long will I take part?
- 5 Years
- Phase
- Observational
- 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
Study population: Patients with dysfunctional hemodialysis vascular access referred for PTA or patients who received maintenance hemodialysis will be prospectively enrolled.
Who may be able to join
- age from 20-99 years old, undergoing regular hemodialysis for at least six months.
Who cannot join
- (1) patients received regular dialysis less than 6 months
- (2) patients with clinical evidence of acute or chronic inflammation, decompensated heart failure, recent myocardial infarction, or unstable angina in recent 3 months
Trial locations and contacts
1 site in 1 country.
Taiwan1 site, 1 recruiting
- Recruiting
National Taiwan University Hospital Hsinchu Branch
Hsinchu
Chiu-kuei Nien
Chih-Cheng Wu, M.D.
About this study
Official title: Investigating the Impact of Blood Pressure Variability on the Outcomes of Hemodialysis Vascular Access
Hemodialysis vascular access dysfunction continues to be a major source of morbidity and mortality in patients with ESRD. Thrombosis is the most common cause of secondary vascular access failure Although intimal hyperplasia at the outflow vein is the most common cause of thrombosis, 20-40% of thrombosis may develop secondary without underlying anatomic abnormalities. Low-flow states secondary to low BP have been proposed to precipitate access thrombosis. In previous studies, lower pre- and post- dialysis SBP are associated with a higher rate of access thrombosis. Nonetheless, high blood pressure is also a well-known risk factor for arteriosclerosis, intimal hyperplasia, and thrombotic vascular events. In dialysis patients, the relation between blood pressure and thrombosis seems to be more complex, and few studies have delineated the effect of blood pressure in a systematic manner.
In addition to the static component of blood pressure, blood pressure variability (BPV) is increasingly accepted as a novel risk factors for vascular disease. BPV is categorized as either long or short term. In dialysis patients, long-term BPV is typically defined on the basis of BP measurements taken at the start of hemodialysis (inter-dialysis BPV); short-term BPV is usually considered in terms of variability during hemodialysis (intra-dialysis BPV). BP variability is increased in ESRD patients and is associated with adverse outcomes. To the best of our knowledge, only one study by Cheung et al focused on intra-dialytic BPV, which found intradialytic hypotension to be a risk factor for access thrombosis. Nonetheless, access thrombotic events rarely occur during the dialysis session. It remained unclear that if inter-dialysis BPV is a more relevant factor for access thrombosis. Answer to this question is of clinical significance because the optimal BP target after PTA remained unknown. In this study, we aimed to investigate the effect of BP variability on the outcomes of hemodialysis vascular access, major cardiovascular events in maintenance hemodialysis patients. We also aimed to evaluate the determinants of BPV in hemodialysis patients, including medication, frailty, fluid status and autonomic function. The impact of autonomic function and frailty on the outcomes of vascular access and cardiovascular events will be evaluated as well.
Read the detailed description
Hemodialysis vascular access dysfunction continues to be a major source of morbidity and mortality in patients with ESRD1. After the publication of the dialysis outcome quality initiative guidelines, endovascular interventions gradually replaced surgical revisions as the primary treatment of dysfunctional dialysis access2. Although percutaneous transluminal angioplasty (PTA) can achieve a high success rate, recurrent stenosis and thrombosis are usually inevitable3, 4. As a result, repeated interventions are required and cause a substantial financial burden on the health care system. Intimal hyperplasia at the outflow vein is the most common cause of vascular access dysfunction5. Thrombosis may develop secondary to outflow venous stenosis, but it can also develop without underlying anatomic abnormalities6.
Thrombosis is the most common cause of secondary vascular access failure (i.e., failure of functioning vascular access) and is associated with luminal stenosis in 60% to 80% of cases. However, because 20% to 40% of cases of access thrombosis occur in the absence of stenosis, and because not all stenotic accesses thrombose, other factors must contribute to access thrombosis.7 Among other factors, low-flow states secondary to low BP have been proposed to precipitate access thrombosis.8 These putative causes of access thrombosis make intuitive sense, but few studies have actually examined these factors in a systematic manner.
The relation between blood pressure and access thrombosis is complex. Very few studies have addressed on this issue. Unlike in the general population, blood pressure is not linearly associated with adverse outcomes in hemodialysis patients. Traditionally, high blood pressure is a well-known risk factors of intimal hyperplasia and thrombosis. Nonetheless, lower BP may also lead to decreased access blood flow, which has been shown to independently predict subsequent access thrombosis.9 In addition to the static component of blood pressure, blood pressure variability (BPV) is closely associated with adverse outcomes in patients with or at risk of vascular disease than 'usual' BP.10 They may play a causal role in the progression of organ damage and in triggering vascular events. BPV is categorized as either long or short term, based on the time interval over which it is considered.11 Long term BPV is usually measured as visit-to-visit BPV and can be considered in intervals of days, weeks or months. In the dialysis patients, the long term BPV is typically defined on the basis of BP measurements taken at the start of hemodialysis treatment (inter-dialytic BPV). Short-term BPV is usually measured by ambulatory BP monitoring or during specified short-time intervals. Among dialysis patients, short-term BPV can be considered in terms of variability that occurred during hemodialysis treatment (intra-dialytic BPV).
4 BP variability is known to be increased in patients with ESRD.12 Among patients undergoing hemodialysis, potential causes of high BP variability such as baroreceptor dysfunction, aortic stiffness, and variations in intravascular volume, as well as plausible outcomes such as cerebral small-vessel disease, cerebral hemorrhage, and cardiac sudden death are increased compared to the general population.13, 14 Therefore, increased BP variability may provide a potential explanation for access thrombosis among patients undergoing hemodialysis. Currently, only one study by Cheung et al has focused on the effect of BP variability. Lower pre-and post- dialysis SBP is associated with a higher rate of access thrombosis, consistent with previous studies.15, 16 More importantly, intradialytic hypotension is also a risk factor for access thrombosis and may account for some of the 20% to 40% of cases without obvious structural abnormalities.16 Nonetheless, most access thrombotic events did not occur during the dialysis session. It remained unclear if inter-dialysis BP variability is also a risk factor for vascular access thrombosis. The answer to these queries is of therapeutic relevance because the achievement of the recommended target BP in dialysis patients may be associated with higher rates of inter- or intra-dialytic hypotension.17 Accordingly, we aimed to investigate the effect of intra-dialysis BPV, inter-dialysis BPV, and intra-dialysis hypotension on thrombosis of hemodialysis vascular access.We also aimed to evaluate the determinants of BPV in hemodialysis patients, including medication, frailty, fluid status and autonomic function. The impact of autonomic function and frailty on the outcomes of vascular access and cardiovascular events will be evaluated as well.
- Being tested
- Measure: BP measurements, inter-dialysis BP variability, intra-dialysis hypotension
- Keywords
- hemodialysis access failure, blood pressure
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Measure: BP measurements, inter-dialysis BP variability, intra-dialysis hypotensionDiagnostic test
BP will be measured at the beginning and end of each dialysis session in a seated position by a trained dialysis nurse in accordance with the routine unit practice and entered into an electronic database. BP was measured using validated oscillometric BP monitor equipped in hemodialysis machines (Fresenius 4008S or Nikisso DBB-05), which were maintained as per dialysis unit protocols.
| Study group | Role | What they receive |
|---|---|---|
| Total study cohort | Patients with dysfunctional hemodialysis vascular access referred for PTA or patients who received maintenance hemodialysis will be prospectively enrolled. Receives: Diagnostic Test: Measure: BP measurements, inter-dialysis BP variability, intra-dialysis hypotension |
What is being measured
The primary outcome is the main question the study is designed to answer.
Vascular access thrombosis
An access that had clotted without blood flow
Measured: 30 months
Secondary outcomes (4)
Post-intervention primary patency
the time until next intervention on the access of any kind
Measured: 30 months
Post-intervention secondary patency
time from enrollment until surgical revision or abandonment of the access
Measured: 30 months
stroke (both ICH and infarction)
time from enrollment to the first event
Measured: 5 years
major cardiovascular events
CV death, non-fatal MI, non-fatal stroke, and acute/critical limb ischemia
Measured: 5 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted5 Jan 2021
- Study start1 Jan 2018
- Primary completion31 Dec 2022 (estimated)
- Study completion31 Dec 2022 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (2)Papers the sponsor has linked to this study.
- Other trials for Hemodialysis Access 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
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 1,300 participants (estimated)
- Target duration
- 5 Years
Sponsor and investigators
- Lead sponsor
- National Taiwan University Hospital Hsin-Chu Branch
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04692636
- Sponsor's protocol ID
- 106-033-E
- Status last verified
- Dec 2020
- First submitted
- 29 Dec 2020
- Last updated
- 5 Jan 2021
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Hsieh MY, Tsai LK, Hsu RY, Chen MK, Yang CW, Chuang SY, Lai TJ, Cheng HM, Wu CC. Systolic BP Variability and Risk of Ischemic Stroke in Patients Receiving Hemodialysis. Clin J Am Soc Nephrol. 2026 Aug 31. doi: 10.2215/CJN.0000001210. Online ahead of print.
PubMed 42671894Hsieh MY, Chuang SY, Lee CK, Luo CM, Cheng CH, Liao MT, Lin PL, Yang TF, Wu CC. Risks and outcomes of critical limb ischemia in hemodialysis patients: a prospective cohort study. Clin Kidney J. 2022 Dec 8;16(3):585-595. doi: 10.1093/ckj/sfac263. eCollection 2023 Mar.
PubMed 36865012
Study at a glance
From the registry record, last updated by the sponsor on 5 Jan 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Investigating the Impact of Blood Pressure Variability on the Outcomes of Hemodialysis Vascular Access
- ClinicalTrials.gov ID
- NCT04692636
- Acronym / sponsor ID
- 106-033-E
- Keywords
- hemodialysis access failure, blood pressure
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 1,300 participants (estimated)
- Lead sponsor
- National Taiwan University Hospital Hsin-Chu BranchUniversity, hospital or other
- Study start
- 1 Jan 2018 (actual)
- Primary completion
- 31 Dec 2022 (estimated)
- Study completion
- 31 Dec 2022 (estimated)
- First posted
- 5 Jan 2021 (actual)
- 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 vascular access dysfunction continues to be a major source of morbidity and mortality in patients with ESRD. Thrombosis is the most common cause of secondary vascular access failure Although intimal hyperplasia at the outflow vein is the most common cause of thrombosis, 20-40% of thrombosis may develop secondary without underlying anatomic abnormalities. Low-flow states secondary to low BP have been proposed to precipitate access thrombosis. In previous studies, lower pre- and post- dialysis SBP are associated with a higher rate of access thrombosis. Nonetheless, high blood pressure is also a well-known risk factor for arteriosclerosis, intimal hyperplasia, and thrombotic vascular events. In dialysis patients, the relation between blood pressure and thrombosis seems to be more complex, and few studies have delineated the effect of blood pressure in a systematic manner.
In addition to the static component of blood pressure, blood pressure variability (BPV) is increasingly accepted as a novel risk factors for vascular disease. BPV is categorized as either long or short term. In dialysis patients, long-term BPV is typically defined on the basis of BP measurements taken at the start of hemodialysis (inter-dialysis BPV); short-term BPV is usually considered in terms of variability during hemodialysis (intra-dialysis BPV). BP variability is increased in ESRD patients and is associated with adverse outcomes. To the best of our knowledge, only one study by Cheung et al focused on intra-dialytic BPV, which found intradialytic hypotension to be a risk factor for access thrombosis. Nonetheless, access thrombotic events rarely occur during the dialysis session. It remained unclear that if inter-dialysis BPV is a more relevant factor for access thrombosis. Answer to this question is of clinical significance because the optimal BP target after PTA remained unknown. In this study, we aimed to investigate the effect of BP variability on the outcomes of hemodialysis vascular access, major cardiovascular events in maintenance hemodialysis patients. We also aimed to evaluate the determinants of BPV in hemodialysis patients, including medication, frailty, fluid status and autonomic function. The impact of autonomic function and frailty on the outcomes of vascular access and cardiovascular events will be evaluated as well.
Detailed description
Hemodialysis vascular access dysfunction continues to be a major source of morbidity and mortality in patients with ESRD1. After the publication of the dialysis outcome quality initiative guidelines, endovascular interventions gradually replaced surgical revisions as the primary treatment of dysfunctional dialysis access2. Although percutaneous transluminal angioplasty (PTA) can achieve a high success rate, recurrent stenosis and thrombosis are usually inevitable3, 4. As a result, repeated interventions are required and cause a substantial financial burden on the health care system. Intimal hyperplasia at the outflow vein is the most common cause of vascular access dysfunction5. Thrombosis may develop secondary to outflow venous stenosis, but it can also develop without underlying anatomic abnormalities6.
Thrombosis is the most common cause of secondary vascular access failure (i.e., failure of functioning vascular access) and is associated with luminal stenosis in 60% to 80% of cases. However, because 20% to 40% of cases of access thrombosis occur in the absence of stenosis, and because not all stenotic accesses thrombose, other factors must contribute to access thrombosis.7 Among other factors, low-flow states secondary to low BP have been proposed to precipitate access thrombosis.8 These putative causes of access thrombosis make intuitive sense, but few studies have actually examined these factors in a systematic manner.
The relation between blood pressure and access thrombosis is complex. Very few studies have addressed on this issue. Unlike in the general population, blood pressure is not linearly associated with adverse outcomes in hemodialysis patients. Traditionally, high blood pressure is a well-known risk factors of intimal hyperplasia and thrombosis. Nonetheless, lower BP may also lead to decreased access blood flow, which has been shown to independently predict subsequent access thrombosis.9 In addition to the static component of blood pressure, blood pressure variability (BPV) is closely associated with adverse outcomes in patients with or at risk of vascular disease than 'usual' BP.10 They may play a causal role in the progression of organ damage and in triggering vascular events. BPV is categorized as either long or short term, based on the time interval over which it is considered.11 Long term BPV is usually measured as visit-to-visit BPV and can be considered in intervals of days, weeks or months. In the dialysis patients, the long term BPV is typically defined on the basis of BP measurements taken at the start of hemodialysis treatment (inter-dialytic BPV). Short-term BPV is usually measured by ambulatory BP monitoring or during specified short-time intervals. Among dialysis patients, short-term BPV can be considered in terms of variability that occurred during hemodialysis treatment (intra-dialytic BPV).
4 BP variability is known to be increased in patients with ESRD.12 Among patients undergoing hemodialysis, potential causes of high BP variability such as baroreceptor dysfunction, aortic stiffness, and variations in intravascular volume, as well as plausible outcomes such as cerebral small-vessel disease, cerebral hemorrhage, and cardiac sudden death are increased compared to the general population.13, 14 Therefore, increased BP variability may provide a potential explanation for access thrombosis among patients undergoing hemodialysis. Currently, only one study by Cheung et al has focused on the effect of BP variability. Lower pre-and post- dialysis SBP is associated with a higher rate of access thrombosis, consistent with previous studies.15, 16 More importantly, intradialytic hypotension is also a risk factor for access thrombosis and may account for some of the 20% to 40% of cases without obvious structural abnormalities.16 Nonetheless, most access thrombotic events did not occur during the dialysis session. It remained unclear if inter-dialysis BP variability is also a risk factor for vascular access thrombosis. The answer to these queries is of therapeutic relevance because the achievement of the recommended target BP in dialysis patients may be associated with higher rates of inter- or intra-dialytic hypotension.17 Accordingly, we aimed to investigate the effect of intra-dialysis BPV, inter-dialysis BPV, and intra-dialysis hypotension on thrombosis of hemodialysis vascular access.We also aimed to evaluate the determinants of BPV in hemodialysis patients, including medication, frailty, fluid status and autonomic function. The impact of autonomic function and frailty on the outcomes of vascular access and cardiovascular events will be evaluated as well.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 5 Years
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Total study cohort | – | Diagnostic Test: Measure: BP measurements, inter-dialysis BP variability, intra-dialysis hypotensionPatients with dysfunctional hemodialysis vascular access referred for PTA or patients who received maintenance hemodialysis will be prospectively enrolled. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients with dysfunctional hemodialysis vascular access referred for PTA or patients who received maintenance hemodialysis will be prospectively enrolled.
Key inclusion criteria (1 listed)
- age from 20-99 years old, undergoing regular hemodialysis for at least six months.
Key exclusion criteria (2 listed)
- (1) patients received regular dialysis less than 6 months
- (2) patients with clinical evidence of acute or chronic inflammation, decompensated heart failure, recent myocardial infarction, or unstable angina in recent 3 months
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 |
|---|---|---|
| Measure: BP measurements, inter-dialysis BP variability, intra-dialysis hypotensionBP will be measured at the beginning and end of each dialysis session in a seated position by a trained dialysis nurse in accordance with the routine unit practice and entered into an electronic database. BP was measured using validated oscillometric BP monitor equipped in hemodialysis machines (Fresenius 4008S or Nikisso DBB-05), which were maintained as per dialysis unit protocols. | Diagnostic test | Total study cohort |
Primary outcome
Vascular access thrombosis
Time frame: 30 months
An access that had clotted without blood flow
4 secondary outcomes
Post-intervention primary patency
Time frame: 30 months
Post-intervention secondary patency
Time frame: 30 months
stroke (both ICH and infarction)
Time frame: 5 years
major cardiovascular events
Time frame: 5 years
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Jan 2021.
- Derived from this study: PubMed 42671894Hsieh MY, Tsai LK, Hsu RY, Chen MK, Yang CW, Chuang SY, Lai TJ, Cheng HM, Wu CC. Systolic BP Variability and Risk of Ischemic Stroke in Patients Receiving Hemodialysis. Clin J Am Soc Nephrol. 2026 Aug 31. doi: 10.2215/CJN.0000001210. Online ahead of print.
- Derived from this study: PubMed 36865012Hsieh MY, Chuang SY, Lee CK, Luo CM, Cheng CH, Liao MT, Lin PL, Yang TF, Wu CC. Risks and outcomes of critical limb ischemia in hemodialysis patients: a prospective cohort study. Clin Kidney J. 2022 Dec 8;16(3):585-595. doi: 10.1093/ckj/sfac263. eCollection 2023 Mar.
- Individual participant dataSharing planned: No
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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.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Hemodialysis Access Failure and Blood Pressure, run by National Taiwan University Hospital Hsin-Chu Branch at 1 site in Taiwan.
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 1 inclusion and 2 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 5 Jan 2021. 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 Taiwan. 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 Mu-Yang Hsieh, M.D. (+88635326151, h11135@hch.gov.tw), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Vascular access thrombosis (time frame: 30 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 NCT04692636, which also lists 2 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 5 Jan 2021.