Factors Associated With Interdialytic Blood Pressure Variability in Maintenance Hemodialysis Patients

NCT ID: NCT01674660

Last Updated: 2012-08-31

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2012-09-30

Study Completion Date

2013-03-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The purpose of this study is to explore the factors associated with interdialytic blood pressure variability in maintenance hemodialysis patients, especially the association between volume status and blood pressure variability.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Hemodialysis patients experience higher rates of cardiovascular morbidity and mortality than the general population and many populations with other chronic diseases. This exceptional risk is explained in part by known risk factors such as diabetes, hypertension, and other uremia-related factors, including vascular calcification and stiffness, autonomic dysfunction, and a high burden of circulating inflammatory mediators. However, additional unidentified risk factors also likely contribute to the disproportionately high prevalence of cardiovascular morbidity in hemodialysis patients. Blood pressure variability may represent one plausible cardiovascular risk factor. Data from nonuremic human populations show an association between greater blood pressure variability and cardiovascular events,nonfatal cardiovascular events,stroke,and increased left ventricular mass. There has been comparatively little work examining the causes and effects of blood pressure variability in hemodialysis populations. So the purpose of this study is to explore the factors associated with interdialytic blood pressure variability in maintenance hemodialysis patients, especially the association between volume status and blood pressure variability.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Kidney Failure, Chronic

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

hemodialysis blood pressure variability volume status

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

CASE_CONTROL

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

volume status

volume status:group1 over volume status,group2 normal volume status,group3 low volume status

No interventions assigned to this group

night blood pressure

night blood pressure:group1 nondipper,group2 dipper,group3 extreme dipper,group4 riser

No interventions assigned to this group

interdialysis weight gain

interdialysis weight gain:group1 \>5% dry weight,group2 \<5% dry weight

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* age 18 years or older
* receipt of thrice-weekly in-center hemodialysis
* no anticipation of imminent(\<6 months)living related kidney transplant
* not transfer of care to a nonparticipating facility
* no dialytic modality change

Exclusion Criteria

* who missed \>2 hemodialysis treatments over 1 month
* abused drugs
* severe anemia,malnutrition,chronic atrial fibrillation
* body mass index of 40 \>kg/m2
Minimum Eligible Age

24 Years

Maximum Eligible Age

85 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Beijing Chao Yang Hospital

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Ma Weihua

Principal Investigater

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Ma WH weihua, Master

Role: PRINCIPAL_INVESTIGATOR

Beijing Chao Yang Hospital

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Nephrology, dialysis center,Beijing Chaoyang Hospital

Beijing, Beijing Municipality, China

Site Status

Countries

Review the countries where the study has at least one active or historical site.

China

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Cui TG Taigen, Dr.

Role: CONTACT

Phone: 010-85231510

Email: [email protected]

Ma WH Weihua, Master

Role: CONTACT

Phone: 010-85231952

Email: [email protected]

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Ma WH Weihua, Master

Role: primary

Cui TG taigen, Dr.

Role: backup

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

19860805

Identifier Type: REGISTRY

Identifier Source: secondary_id

BeijingCYH

Identifier Type: -

Identifier Source: org_study_id