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NCT03649178Completed

Dietary Salt in Rheumatoid Arthritis

Inflammatory and Vascular Response to Dietary Salt in Rheumatoid Arthritis

Source: ClinicalTrials.gov · Last updated 30 Jul 2026

Brief summary (registry, in English)

In this study investigators propose to address the following hypotheses: 1) Reduction in dietary sodium will decrease inflammation in patients with rheumatoid arthritis (RA). 2) Reduction in dietary sodium will decrease blood pressure in patients with RA. 3) Reduction in dietary sodium will decrease tissue sodium in patients with RA.

Status (registry)
Completed
Study type
Interventional
Enrollment
18 (actual)
First submitted
23 Aug 2018
Start date
2 Jan 2020
Primary completion date
30 Sept 2024
Lead sponsor
Vanderbilt University Medical Center
NCT number
NCT03649178

What you commit to

  • Study type: Interventional
  • Participants enrolled: 18
  • From 2 Jan 2020 to the primary completion date, 30 Sept 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Receiving dialysis
  • Organ or bone marrow transplant
  • Diabetes mellitus treated with an insulin pump
  • Major surgery within the previous 3 months
  • Presence of a condition that could make 24-hour blood pressure monitoring difficult: atrial fibrillation, inability to operate machine, receiving anticoagulants, presence of a condition that in the opinion of the investigator may be exacerbated by blood pressure cuff inflation (e.g., lymphedema).

Other illness

  • Taking diuretics, uncontrolled hypertension (\>160/100 mmHg), or cardiac failure requiring treatment.
  • Severe co-morbid conditions such as active cancer likely to compromise study participation

Other

  • Pregnancy
  • Severe edema (as judged by the investigator)
  • Unwillingness, or other inability, to cooperate
  • Contraindication to MRI

Who the study is looking for

  • Male and female patients older than 18 years who are willing to participate.
  • Satisfy the ACR criteria for the diagnosis of RA.
  • Have stable disease activity as evidenced by no clinically meaningful change in immunomodulating or corticosteroid therapy in the past 1 month.
  • Have moderate disease activity as reflected by a minimum of 3 swollen and tender joints.

Age in the registry: 18 years to 80 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Vanderbilt University Medical Center
Coordinator of this site? Confirm its status
NashvilleUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.