Clinical trial Recruiting at 2 sites Phase 4 Interventional Ages 18 and up

Impact of dietary salt on skin sodium and inflammatory skin disease

Official title: The Impact of Salt Intake on Sodium in the Skin and Inflammatory Skin Disease

Run by University of California, San Francisco · NCT07487831 · Data updated 2026-11-12

We’re testing whether lowering salt and taking salt tablets changes skin sodium and symptoms in eczema and psoriasis.

Quick facts

PhasePhase 4
Study typeInterventional
Ages18 Years and up
SexAll
Enrollment50 (estimated)
SponsorUniversity of California, San Francisco
Academic / other
Drugs / interventionsdupilumab
Locations2 sites (San Francisco, California and 1 other locations)
StatusRecruiting
StartedJuly 14, 2026
Main results expectedMarch 17, 2028
Study endsMarch 17, 2028
Registry record updatedSeptember 9, 2026
Trial IDNCT07487831 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults with atopic dermatitis or psoriasis who can undergo MRI and are willing to follow a low-sodium diet.

Probably not a fit

Patients unable or unwilling to adhere to a low-sodium diet or whose skin disease is unrelated to sodium balance may not benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This trial tests whether reducing dietary sodium affects skin sodium levels and disease severity in people with atopic dermatitis or psoriasis, using a noninvasive sodium MRI to measure skin sodium. Participants follow a DASH-style low-sodium diet and alternate between daily sodium chloride tablets and placebo in a randomized cross-over design over 13 weeks, with multiple clinic visits for questionnaires and samples. The study aims to generate pilot data to explore potential links between salt intake, skin sodium content, and inflammatory skin disease activity. Healthy controls will have skin sodium scans only at baseline, while patients with eczema or psoriasis will track symptoms alongside biomarker data.

Why it matters

Potential benefit: If successful, it could clarify whether salt reduction helps reduce skin inflammation and disease severity.

How similar studies have gone: Prior work suggests a plausible link between sodium intake and skin inflammation, but this trial will provide pilot data on feasibility and potential effects using a cross-over design.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Participants ages 18 years
* Willing and able to undergo non-contrast MRI.

Exclusion Criteria:

* Contraindications to MRI (such as cardiac pacemakers, claustrophobia, non-compatible intracranial vascular clips, IUDs, or other implants)
* A cardiac event in the past 6 months
* Impaired function of the liver or kidney (glomerular filtration rate \<60 mL/min)
* Medications that influence sodium excretion (e.g., diuretics or SGLT2 inhibitors)
* Antibiotic or immunomodulatory medications within the last month
* Contraindications to sodium tablets

(Topical medications used exclusively on the head/neck or hands/feet (e.g., antifungal nail treatment, antidandruff shampoo, acne cleansers) are acceptable. Topical and systemic eczema treatments are acceptable if the participant has been on a stable dose for at least 2 months and still meets the severity entry criteria. Patients on dupilumab will not be excluded if they have been on dupilumab for at least two months and still meet the disease severity inclusion criteria.)

Where it's running

  • UCSF Mt Zion Campus
    San Francisco, California, United States
    Recruiting
  • San Francisco VA Medical Center
    San Francisco, California, United States
    Recruiting

Study contacts

  • Principal investigator: Katrina Abuabara, MD — University of California, San Francisco
  • Study coordinator: Alicia Hamblin
  • Email: Alicia.Hamblin@ucsf.edu
  • Phone: 925-549-7889

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.