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IgA Nephropathy (IgAN)NCT07022574

Autoimmune Protocol Diet Intervention on Proteinuria in IgA Nephropathy Patients

A study testing Low inflammation diet intervention in people with IgA Nephropathy (IgAN), run by University of California, Los Angeles at 1 site in United States.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

This study at UCLA Center for Health Sciences is testing whether the Autoimmune Protocol (AIP) diet can lower protein levels in the urine of people with IgA Nephropathy (IgAN), a common kidney disease that can lead to kidney failure. Read more about this study

Who is it for?
Ages 18 to 65 years
Conditions the study is for
IgA Nephropathy (IgAN)
What is being tested?
Low inflammation diet intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
0 participants
Where
1 siteUnited States
Study dates
1 Feb 2026to 1 Dec 2027
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 to 65 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Age 18-65
  • Diagnosed with IgA Nephropathy (IgAN)
  • Active disease with urine protein/creatinine ratio ≥ 1
  • Stable ARB or ACE inhibitor for at least 1 month prior
  • GFR > 30
  • Not on Budesonide 1 month prior or during study

Who cannot join

  • Inability to comply with dietary or follow-up requirements
  • Participation in other interventional studies
  • Significant comorbidities interfering with study participation -

Trial locations and contacts

1 site in 1 country.

United States1 site
  • UCLA

    Manhattan Beach, California, 90266

Other trials in United States

About this study

Official title: Evaluating the Impact of Autoimmune Protocol Diet on Proteinuria in Patients With IgA Nephropathy

This study at UCLA Center for Health Sciences is testing whether the Autoimmune Protocol (AIP) diet can lower protein levels in the urine of people with IgA Nephropathy (IgAN), a common kidney disease that can lead to kidney failure. The AIP diet avoids foods that may cause inflammation (like dairy, grains, and sugar) for 8 weeks, then gradually reintroduces them over 4 months. We're enrolling 30 adults aged 18-65 with IgAN and protein in their urine to try this diet for 6 months. Participants will track their urine protein daily at home, keep a food log, and have monthly lab checkups, with support from a diet expert. The main goal is to see if the diet reduces urine protein by 20% or more, which could slow disease progression and reduce the need for treatments like dialysis. This exploratory study aims to find out if diet changes can help manage IgAN.

Read the detailed description

This study, conducted at UCLA Center for Health Sciences, explores the potential of the Autoimmune Protocol (AIP) diet as a novel intervention for IgA Nephropathy (IgAN), a chronic kidney condition driven by immune system dysfunction. IgAN involves the deposition of galactose-deficient IgA1 (Gd-IgA1) in the glomeruli, triggering inflammation and progressive renal damage. Emerging evidence points to the gut, particularly the gastric-associated lymphoid tissue (GALT), as a key site where aberrant immune responses initiate this process. The AIP diet, a structured elimination and reintroduction plan, has shown promise in reducing inflammation in other autoimmune conditions like inflammatory bowel disease and rheumatoid arthritis. This study builds on a clinical observation of proteinuria reduction in an IgAN patient post-renal transplant following AIP diet adoption, aiming to test its broader applicability.

The intervention spans 6 months and is divided into two phases. The initial 8-week elimination phase removes foods known to provoke inflammation-such as dairy, grains, legumes, nightshades, and refined sugars-which may influence GALT activity and Gd-IgA1 production. This is followed by a 4-month reintroduction phase, where foods are systematically re-added to assess individual tolerances and their impact on renal markers. Unlike pharmacological approaches targeting downstream effects (e.g., ACE inhibitors) or upstream Gd-IgA1 production (e.g., Budesonide), the AIP diet offers a non-invasive strategy to modulate mucosal immunity. The study hypothesizes that reducing dietary inflammatory triggers could decrease immune complex formation, thereby lowering proteinuria and potentially altering disease trajectory.

Participants will receive extensive support, including initial training from a certified AIP nutritionist, two AIP cookbooks, and ongoing guidance via email or phone consultations. Daily home monitoring involves urine dipsticks to measure protein levels, complemented by weekly food journaling to track adherence and identify correlations with urinary changes. Monthly in-person visits will collect blood and urine samples for laboratory analysis, including Chem7, to assess renal function and metabolic health. This single-center, open-label design prioritizes feasibility and real-world applicability, with no placebo group, as the focus is on detecting a signal of efficacy in a small cohort.

The study's scientific foundation rests on the multi-hit pathogenesis model of IgAN, where mucosal immune dysregulation in the gut precedes renal injury. By targeting GALT, which constitutes a significant portion of the body's immune interface, the AIP diet may reduce the production of pathogenic IgA1. Previous dietary studies in IgAN, such as gluten-free interventions, have hinted at gut-renal connections, but none have tested a comprehensive low-inflammation approach like AIP. Technical considerations include the use of the urinary protein-to-creatinine ratio as a reliable, non-invasive marker of proteinuria, validated in nephrology research for its sensitivity to treatment effects.

Safety is a priority, with risks limited to mild discomfort from blood draws (e.g., bruising), dietary adjustment challenges, and minimal inconvenience from daily urine testing. Adverse events will be logged and reported per IRB standards, with monthly lab monitoring ensuring early detection of any renal or metabolic concerns. The study's exploratory nature and small sample size (n=30) aim to generate preliminary data, with statistical power calculated to detect a 20% proteinuria reduction.

Funded by individual donations, this research is independent of commercial interests, covering costs for lab tests, dietary education, and participant support materials. Findings will contribute to the growing understanding of diet's role in kidney disease management, with results shared through peer-reviewed journals and scientific conferences. This study represents a first step toward integrating dietary strategies into IgAN care, offering a low-risk, patient-centered complement to existing therapies.

Being tested
Low inflammation diet intervention
Keywords
IgA Nephropathy, Kidney disease, Low inflammation diet, Autoimmune Protocol Diet, Protein in urine, Autoimmune Kidney Disease, Elimination diet, Diet and Kidney disease
Medical subject headings
Glomerulonephritis, IGA, Kidney Diseases, Proteinuria

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Low inflammation diet interventionBehavioural

    Also called Autoimmune Protocol Diet

    Autoimmune Protocol Diet intervention

Study groups in NCT07022574
Study groupRoleWhat they receive
AIP Intervention armExperimentalAutoimmune Protocol Diet intervention
Receives: Behavioral: Low inflammation diet intervention

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change from Baseline Urinary Protein to Creatine Ratio at 6months

    Primary Outcome Measure

    1. Change in Urinary Protein-to-Creatinine Ratio
    • Description: This measure assesses the reduction in proteinuria, a key indicator of IgA Nephropathy (IgAN) activity, following the Autoimmune Protocol (AIP) diet intervention. The urinary protein-to-creatinine ratio (UPCR) will be calculated from spot urine samples collected at baseline and monthly intervals. The study aims to detect a reduction of 20% or greater from baseline, reflecting a clinically meaningful improvement in kidney function.
    • Time Frame: Baseline to 6 months (end of study).
    • Measurement: Expressed as grams of protein per gram of creatinine (g/g), analyzed via laboratory testing of urine samples.

    Measured: 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Jun 2025
  2. Study start1 Feb 2026 (estimated)
  3. Primary completion1 Dec 2027 (estimated)
  4. Study completion1 Dec 2027 (estimated)

Why it stopped: Unable to recruit

Resources

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
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07022574
Sponsor's protocol ID
IRB# 25-0145
Status last verified
Jul 2026
First submitted
8 Jun 2025
Last updated
27 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No: IPD that underlie results in a publication.

Publications

  • Konijeti GG, Kim N, Lewis JD, Groven S, Chandrasekaran A, Grandhe S, Diamant C, Singh E, Oliveira G, Wang X, Molparia B, Torkamani A. Efficacy of the Autoimmune Protocol Diet for Inflammatory Bowel Disease. Inflamm Bowel Dis. 2017 Nov;23(11):2054-2060. doi: 10.1097/MIB.0000000000001221.

    PubMed 28858071

Questions about this trial

What is this clinical trial studying?

A study testing Low inflammation diet intervention in people with IgA Nephropathy (IgAN), run by University of California, Los Angeles at 1 site in United States.

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 6 inclusion and 3 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: withdrawn, as of the sponsor's last update on 27 Jul 2026. 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 United States. 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?

The study was withdrawn before enrolling participants, so there are no results.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change from Baseline Urinary Protein to Creatine Ratio at 6months (time frame: 6 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 NCT07022574, which also lists 1 linked publication.

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 27 Jul 2026.

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