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WITHDRAWN
NA
INTERVENTIONAL
2015-01-31
2016-05-31
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.
Changes in Acid Base Status During High Salt Intake
NCT01655953
Dietary Acid Load, Kidney Function and Disability in Elderly
NCT02691663
Analysis of Calcium Balance in Chronic Kidney Disease
NCT00974532
Arterial pH and Total Body Nitrogen Balances in APD
NCT00586131
Reduction of Metabolic Acidosis in Patients With Chronic Kidney Disease in Stage 4 and 5
NCT05970094
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.
RANDOMIZED
CROSSOVER
DIAGNOSTIC
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
feeding a high acid diet x 24 hrs
2 diets, one low and one high net acid loads
high or low acid diet
high or low acid diets
low acid diet
high or low acid diet
high or low acid diets
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
high or low acid diet
high or low acid diets
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* able to come to UCSF for study
Exclusion Criteria
* Hg \< 10
* abnormal screening labs
* anyone unable to follow study directions
18 Years
65 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
optimal wellness labs
UNKNOWN
University of California, San Francisco
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
lynda frassetto, md
Role: PRINCIPAL_INVESTIGATOR
University of California, San Francisco
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
UCSF
San Francisco, California, United States
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.
UPH&DNAE
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.