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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT03607500
Other study ID # HUM00134686
Secondary ID P30DK089503
Status Terminated
Phase N/A
First received
Last updated
Start date August 22, 2019
Est. completion date August 16, 2021

Study information

Verified date January 2023
Source University of Michigan
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

One possible reason that weight gain after transplant may interfere with new kidney function is due to the enlargement of a kidney structure called the glomerulus. The researchers believe that modest caloric intake reduction (CIR) early after kidney transplantation can reduce the enlargement (hypertrophy) of the glomerulus associated with kidney transplantation and may improve long term allograft survival, by reducing glomerular hypertrophy mediated progressive glomerulosclerosis.


Recruitment information / eligibility

Status Terminated
Enrollment 1
Est. completion date August 16, 2021
Est. primary completion date August 16, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: - Recipients of kidney transplants where a post perfusion biopsy is obtained - Body Mass Index between 25-30 kg/m2 at the time of randomization - Non-diabetic - Have a smart phone or active internet connection at home Exclusion Criteria: - Patients on dual anti platelet agents or are on oral anti coagulation medication - Patients who have had Bariatric Surgery

Study Design


Intervention

Behavioral:
caloric intake reduction
The caloric intake reduction arm will been seen by the kidney disease dietitian at all clinical visits for the first 3 months (weekly for month 1, every other week for months 2 and 3).

Locations

Country Name City State
United States The University of Michigan Ann Arbor Michigan

Sponsors (2)

Lead Sponsor Collaborator
University of Michigan National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Difference in the Change in Baseline and 3 Month Glomerular Volume Between the Intervention and the Control Arm Post-Perfusion (Time 0 or Study Enrollment) and 3 months
Primary Difference in the Number of Glomerular Ki67 Positive Cells Between the Intervention and the Control Arm 3 month protocol biopsies will be stained with monoclonal antibodies against Ki67 to identify actively dividing cells and counted manually. 3 months
Primary Difference in the Number of Glomerular DAPI Positive (Nuclei) Between the Intervention and the Control Arm 3 month protocol biopsies will be stained with monoclonal antibodies against DAPI to identify nucleated cells in the glomerulus and counted manually. 3 months
Primary Difference in the Number of TLE4 Positive (Podocyte Nuclei) Between the Intervention and the Control Arm 3 month protocol biopsies will be stained with monoclonal antibodies against TLE4 to identify podocytes and counted manually. 3 months
Primary Differences in Podocyte Detachment Rate Between the Intervention and the Control Arm Urine samples obtained at the time of 3-month protocol biopsies will be utilized to compare the urinary podocin mRNA to urinary creatinine ratio 3 months
Primary Difference in the Podocyte Hypertrophic Stress Between the Intervention and the Control Arm Urine samples obtained at the time of 3-month protocol biopsies will be utilized to compare the urinary podocin mRNA to nephrin mRNA ratio 3 months
Secondary Difference in Glomerular Filtration Rate (GFR) at 3 and 12 Months Between the Intervention and the Control Arm Differences in glomerular filtration rate (GFR) using both creatinine (modified diet in renal disease) as well as serum cystatin C based equations 3 months, 12 months
Secondary Difference in Proteinuria Between the Intervention and the Control Arm Proteinuria measured by laboratory samples Measured through study completion, about 3 months
Secondary Difference in Glycosylated Hemoglobin (HbA1c) Percent in the Intervention and the Control Arms Measure the difference in HbA1c between the two arms during 3 month protocol biopsies 3 months
Secondary Difference in Weight of Participants in the Intervention and Control Arms Weight as measured by pounds 3 months
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