Cohort Study Comparing Short Daily Hemodialysis (HD) With Conventional HD
NCT ID: NCT00182156
Last Updated: 2022-04-15
Study Results
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.
WITHDRAWN
OBSERVATIONAL
2004-10-31
2008-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Pilot Bleeding Study: Risk and Protective Factors Associated With Bleeding in the Hemodialysis Population
NCT00182117
Conventional Hemodialysis vs. Short Daily Hemodialysis (6 Days / Week) and Mechanisms of Blood Pressure Control
NCT00759967
Hemodynamics in Chronic Hemodialysis Patients Undergoing Isolated Ultrafiltration Compared to Conventional Hemodialysis
NCT05642156
Efficacy of Twice Weekly Hemodialysis in Patients With Residual Kidney Function
NCT03874117
Hemodynamic Responses in Hemodialysis Patients to Blood Flow Restriction Using Non-pneumatic Anti-shock Garments
NCT02915627
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
CROSS_SECTIONAL
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
1
conventional HD
No interventions assigned to this group
2
short daily HD
No interventions assigned to this group
3
PD
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
* Patient is minimum of 18 years old
Exclusion Criteria
* Patient is unable to consent due to cognitive difficulties
* Patient refuses consent
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
St. Joseph's Healthcare Hamilton
OTHER
McMaster University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Azim Gangji
Associate professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Azim Gangji, MD
Role: PRINCIPAL_INVESTIGATOR
Clinical Scholar, Medicine
Catherine M Clase, MD
Role: PRINCIPAL_INVESTIGATOR
Associate Professor, Medicine
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
St. Joseph's Healthcare
Hamilton, Ontario, Canada
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
Nephrology Divisional Funds
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.