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NCT04508049Active, not recruiting

A Study to Evaluate Renal Fibrosis Using MRI Techniques

Quantitative Magnetization Transfer MRI for Evaluation of Renal Fibrosis

Source: ClinicalTrials.gov · Last updated 16 Oct 2026

Brief summary (registry, in English)

The purpose of this study is to evaluate whether or not an MRI technique (quantitative magnetization transfer or qMT) in narrowing human kidneys is feasible, reproducible, and predicts recovery.

Status (registry)
Active, not recruiting
Study type
Interventional
Enrollment
24 (actual)
First submitted
6 Aug 2020
Start date
1 Oct 2020
Primary completion date
Dec 2027
Lead sponsor
Mayo Clinic
NCT number
NCT04508049

What you commit to

  • Study type: Interventional
  • Participants enrolled: 24
  • From 1 Oct 2020 to the primary completion date, Dec 2027
  • 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

  • Patients have clinically significant medical conditions within the prior six months: e.g. myocardial infarction, congestive heart failure, stroke, that would, in the opinion of the investigators, compromise the safety of the patient.
  • Requirement for potentially nephrotoxic drugs; e.g., non-steroidal anti-inflammatory drugs.
  • Kidney transplant.

Other illness

  • Uncontrolled hypertension (Systolic BP \>180 mmHg despite therapy).
  • Diabetes requiring insulin or oral hypoglycemic medications.
  • Evidence of hepatitis B or C, or HIV infection.
  • History of deep venous thrombosis within 3 months of enrollment.
  • Any active malignancy and undergoing therapy
  • Another known acute or chronic kidney disease
  • Latex allergy

Lab values

  • Patient has serum creatinine \>2.2 mg/dL for men and \>2.0 mg/dL for women (Caucasians); \>2.4 mg/dL for men and \>2.1 mg/dL for women (African American).
  • Cardiac ejection fraction less than 30%.

Other

  • RVD in a solitary kidney
  • Pacemaker, implantable defibrillator or other contraindication to MRI
  • Inability to comply with breath-hold for 20 seconds
  • Patients are pregnant.
  • Kidney or ureteric stone
  • Federal medical center inmates.

Who the study is looking for

  • Between ages 40 and 80 years old.
  • Patients with hypertension (BP\>140/90 mmHg) and/or requirement for two or more antihypertensive medications for more than 4 weeks.
  • Serum creatinine under 2.2 and 2.0 mg/dL for men and women, respectively (Caucasians). Values for African-American subjects are slightly higher (2.4 mg/dL, males; 2.1 mg/dL females).
  • No contraindications to angiography: severe contrast allergy.
  • No contraindications to no-contrast MR evaluations: e.g. pacemaker or magnetically active metal fragments, claustrophobia.
  • Patients have the ability to comply with protocol
  • Patients are competent and able to provide written informed consent

Age in the registry: 40 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
Mayo Clinic in Rochester
Coordinator of this site? Confirm its status
RochesterUnited StatesUnknown status

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