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NCT07290842Recruiting

The Effects of Dietary Nitrate in Patients With Hypertensive Kidney Injury

Source: ClinicalTrials.gov · Last updated 18 Dec 2025

Brief summary (registry, in English)

The study aims to study the effects of diatery nitrate in patients with hypertension and hypertensive kidney injury. The study is a randomized, placebo-controlled, double-blinded crossover trial. 14-20 patients with hypertension and CKD I-III will be randomized to receive either nitrate or placebo delivered in the form of beetroot juice. Effect variables will be measured before and after a 2 week treatment. After a washout period of 14 days, the subjects are crossed over to the opposite treatment. The study is terminated by measuring effect variables after the second treatment period.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
20 (estimated)
First submitted
18 Nov 2025
Start date
8 Dec 2025
Primary completion date
1 Jan 2028
Lead sponsor
Gødstrup Hospital
NCT number
NCT07290842

What you commit to

  • Study type: Interventional
  • Planned participants: 20
  • From 8 Dec 2025 to the primary completion date, 1 Jan 2028
  • 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

  • • Diagnosis of heart failure, NYHA II-IV
    • Diagnosis of liver failure
    • Diabetes mellitus (all types)
    • Current malignant disease (other than non-melanoma skin cancer)
    • Indicators of other aetiologies of CKD than hypertensive kidney injury, e.g. through kidney biopsy or biochemistry.
    • Previous kidney transplant recipient
    • History of stroke or transient cerebral ischemic attack
    • Current indication of untreated cardiovascular disease, e.g. planned work-up for ischemia.
    • History of myocardial infarction, apart from non-STEMI more than 1 year prior to the study, if the subject is currently revascularized and relevantly medicated.
    • Organic nitrate treatment Diagnosed secondary hypertension other than renal parenchymal hypertension (i.e. renal artery stenosis, primary hyperaldosteronism, low renin hypertension etc.)
  • Conditions treated with medication that investigator finds may interfere with the effect parameters, and cannot be discontinued during the trial (e.g. atrial fibrillation treated with betablockers)

Other

  • Pregnancy or lactation
  • Alcohol abuse (intake above the recommended guidelines from Danish Health Authorities)
  • If, according to the investigator's assessment, the participant is considered unsuitable to participate.

Who the study is looking for

  • Hypertension, treated with a maximum of 2 antihypertensive drugs and unattended office BP \< 150/95 mmHg at the screening visit, or newly diagnosed without antihypertensive treatment by 24-hour BP or home BP measurement (above 130/80 or 135/85 respectively), and unattended office BP \< 160/100 mmHg.
    • CKD I-III based on hypertensive kidney injury. Patients, who previously met the criteria for CKD I within the last 5 years, but no longer has proteinuria after relevant treatment, can also be included. Diagnosis of CKD I can be based on eGFR and either urine albumin/creatine ration or urine-dipstick test with presence of protein.
    • Albumin/creatinine ratio \< 500 mg/g
    • eGFR \> 30 ml/min/1,73m2
    • Body Mass Index (BMI) ≤ 35 kg/m2
    • Able to adhere to dietary regimen
    • Fertile women must use safe contraception (oral contraceptive pill, hormonal or copper intrauterine device, vaginal ring, contraceptive implant, transdermal contraceptive patch or contraceptive injections) or abstinence. Excluded from this are postmenopausal woman without menstrual bleeding for at least 12 months before inclusion, surgically sterilized women and women with surgically sterilized partner.

Age in the registry: 18 years to 70 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
University Clinic in Nephrology and Hypertension, Gødstrup Regional Hospital and Aarhus University
Coordinator of this site? Confirm its status
HerningDenmarkRecruiting

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