Recruiting

Observational Study

Sponsor:

Mayo Clinic

Code:

NCT06886087

Conditions

Living Kidney Donation

Hypertension

Nephrectomy

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Accepted

Study Details

Brief summary:

The goal of this observational study is to learn if PRAT thickness is a marker of visceral obesity and its influence on donors' kidney function and blood pressure in living kidney donors. Population includes male/female, 18 years and up, living kidney donors scheduled for nephrectomy within 6 months. The main area it aims to help in, is future care managing blood pressure and obesity in living kidney transplant donors.

Primary Hypothesis: We hypothesize that Perirenal Fat Thickness (PRAT) may exhibit expansion, remodeling and inflammation that can negatively affect renal outcomes in LKDs.

Researchers will compare PRAT morphology and inflammation in LKDs with low and high PRAT thickness.

We will also correlate PRAT thickness with renal outcomes including vascular remodeling, at the time of donation and worsening hypertension and inadequately increased compensatory GFR of the LKD at 4-6 months post-donation.

Participants will be separated into one of two groups depending on their PRAT measurement and asked to give samples of their blood, perinephric fat, and urine as research samples. Clinically we will abstract data up to 12 months prior and 6 months after their nephrectomy that includes laboratory findings, CT measurements, vitals, exam data, demographics, medical history and current medications.

Conditions

Living Kidney Donation

Hypertension

Nephrectomy

Study ID

NCT06886087

Start date

Feb 10, 2025

Status verified date

Feb, 2026

Completion date

Feb 10, 2028

Anticipated

Primary completion date

Feb 10, 2027

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Accepted

Inclusion Criteria:

  • Participants in this study will be restricted to living kidney transplant donors (LKDs). .

Exclusion Criteria:

  • Those who do not meet Mayo Clinic Rochester's clinical criterion for donor nephrectomy.
  • >10% weight change between the donor evaluation and donor nephrectomy
  • Individuals who are pregnant or are planning to become pregnant
  • Inability to comply with study procedures or any condition that, in the opinion of the investigator, could increase the patient's risk by participating in the study or confound the outcome of the study.

Study Design

Enrollment

100 participants

Anticipated

Interventions and Outcome Measures

Arms

Non-Obese

Participants with a BMI under 30

Obese

Participants with a BMI greater than or equal to 30

Primary outcome measure

  • Proinflammatory Macrophage infiltrations of Perinephric Fat for LKD [ Time Frame: 12 months ]

Central Contacts and Locations

Central contacts

Locations

Mayo Clinic

Recruiting

Rochester, Minnesota, United States, 55905

Contacts

Principal Investigator:

Alexasandra Kukla, MD

More Information

Sponsor

Mayo Clinic

Last update posted

Feb 17, 2026

Last verified

Feb, 2026

Keywords

  • healthy volunteers
  • kidney donation

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Mayo Clinic on 2026-02-17.