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Atorvastatin in the Recipient's Kidney Graft From a Living Donor (ATORV15)

Primary Purpose

Renal Insufficiency

Status
Completed
Phase
Phase 3
Locations
Mexico
Study Type
Interventional
Intervention
Atorvastatin
Placebo
Sponsored by
Instituto Mexicano del Seguro Social
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Renal Insufficiency focused on measuring Kidney Transplantation, Atorvastatin, Human Leukocyte Antigens, Interleukin

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Donors Inclusion Criteria:

  • Accepted as kidney donor
  • Voluntary participation
  • Informed consent accepted
  • 85% fulfillment of atorvastatin treatment
  • Entitlement to the Mexican Institute of Social Security

Donors Exclusion Criteria:

  • Hypersensibility to Atorvastatin
  • Smoking

Recipients Inclusion Criteria:

  • Accepted as kidney recipient
  • Entitlement to the Mexican Institute of Social Security

Recipients Exclusion Criteria:

  • Patients who dropped out from study or withdrew the informed consent
  • Insufficient kidney biopsy

Sites / Locations

  • Western Medical Center, Mexican Institute of Social Security

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Atorvastatin

Placebo

Arm Description

24 patients received oral atorvastatin 40 mg once a day, for 4 weeks.

24 patients received oral placebo 40 mg once a day, for 4 weeks.

Outcomes

Primary Outcome Measures

HLA levels in the kidney graft biopsy
HLA levels were measure by immunohistochemistry, observing alteration between groups.

Secondary Outcome Measures

Renal function
In a blood sample and in a urine 24-hour collection, serum creatinine, serum urea, creatinine clearance, urine output, and proteinuria were measure. Differences in evolution and alteration between the 2 groups were registered.
Kidney graft survival
In a renal biopsy using the Banff classification of renal allograft rejection grades, were assessed histologic and molecular features by microscopy and immunofluorescence. Alterations between groups were registered.
Surgery complications
During surgical procedure and following, any kind of complication was registered.
TNFalpha levels in the kidney graft biopsy
TNFalpha levels were measure by immunohistochemistry, observing alteration between groups.
IL2 and IL6 levels in the kidney graft biopsy
IL2 and IL6 levels were measure by immunohistochemistry, observing alteration between groups.

Full Information

First Posted
August 7, 2015
Last Updated
September 7, 2018
Sponsor
Instituto Mexicano del Seguro Social
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1. Study Identification

Unique Protocol Identification Number
NCT02522117
Brief Title
Atorvastatin in the Recipient's Kidney Graft From a Living Donor
Acronym
ATORV15
Official Title
Effectiveness of Atorvastatin on IL2, IL6, TNFalpha and HLA Levels in the Recipient's Kidney Graft From a Living Donor
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Completed
Study Start Date
August 2015 (undefined)
Primary Completion Date
December 2016 (Actual)
Study Completion Date
January 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Instituto Mexicano del Seguro Social

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Renal insufficiency is a priority disease in the health system, which may require renal replacement therapy based on kidney transplantation, which is considered as therapy of choice. During the procedure of kidney transplantation, the body is subjected to ischemia-reperfusion damage that generates late complications related to graft function. Recently the anti-inflammatory and immunomodulatory effects of statins have been emphasized, which could be beneficial in kidney transplantation.
Detailed Description
Objective: Evaluate the effect of atorvastatin on IL2, IL6, TNFalpha and HLA levels in the recipient's kidney graft from a living donor. Material and methods: Controlled, double-blind trial with 12 months follow-up. Composed of 48 patients, randomized manner, realized at the Transplant Department of Western Medical Center, Mexican Institute of Social Security. Universe was patients accepted as kidney donors and their recipients. Patients included as donors were randomized into two groups (study or control) the intervention was implemented 4 weeks before kidney transplant. During surgical procedure, a biopsy from the recipient's kidney graft was obtained to measure IL-2, IL-6 TNFalpha and HLA by immunohistochemistry, 3 and 12 months after surgery. Recipients kidney function, surgical complications and kidney graft survival were registered. During surgical procedure, 3 and 12 months of following, biopsies were obtain to performed histopathological analysis based on Banff classification of renal allograft rejection grades. The statistical analysis was performed according to the nature of variables, for continuous data using measures of central tendency and dispersion and for the qualitative data with frequencies and percentages. Inferential analysis with student's t-test, and/or Mann-Whitney's U test; chi-square distribution, and/or Fisher's exact test respectively.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Insufficiency
Keywords
Kidney Transplantation, Atorvastatin, Human Leukocyte Antigens, Interleukin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
48 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Atorvastatin
Arm Type
Active Comparator
Arm Description
24 patients received oral atorvastatin 40 mg once a day, for 4 weeks.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
24 patients received oral placebo 40 mg once a day, for 4 weeks.
Intervention Type
Drug
Intervention Name(s)
Atorvastatin
Other Intervention Name(s)
Lipitor
Intervention Description
Patients were assigned to two groups; one of them received oral atorvastatin (study group), and the other homologated placebo (control group) for 4 weeks before transplant. Then IL2, IL6, TNFalpha and HLA levels were assessed in the recipient's kidney graft by visual analog scale at prior reperfusion, and after 3 and 12 months.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Homologated placebo
Intervention Description
Patients were assigned to two groups; one of them received oral atorvastatin (study group), and the other homologated placebo (control group) for 4 weeks before transplant. Then IL2, IL6, TNFalpha and HLA levels were assessed in the recipient's kidney graft by visual analog scale at prior reperfusion, and after 3 and 12 months.
Primary Outcome Measure Information:
Title
HLA levels in the kidney graft biopsy
Description
HLA levels were measure by immunohistochemistry, observing alteration between groups.
Time Frame
12 months
Secondary Outcome Measure Information:
Title
Renal function
Description
In a blood sample and in a urine 24-hour collection, serum creatinine, serum urea, creatinine clearance, urine output, and proteinuria were measure. Differences in evolution and alteration between the 2 groups were registered.
Time Frame
12 months
Title
Kidney graft survival
Description
In a renal biopsy using the Banff classification of renal allograft rejection grades, were assessed histologic and molecular features by microscopy and immunofluorescence. Alterations between groups were registered.
Time Frame
12 months
Title
Surgery complications
Description
During surgical procedure and following, any kind of complication was registered.
Time Frame
12 months
Title
TNFalpha levels in the kidney graft biopsy
Description
TNFalpha levels were measure by immunohistochemistry, observing alteration between groups.
Time Frame
12 months
Title
IL2 and IL6 levels in the kidney graft biopsy
Description
IL2 and IL6 levels were measure by immunohistochemistry, observing alteration between groups.
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Donors Inclusion Criteria: Accepted as kidney donor Voluntary participation Informed consent accepted 85% fulfillment of atorvastatin treatment Entitlement to the Mexican Institute of Social Security Donors Exclusion Criteria: Hypersensibility to Atorvastatin Smoking Recipients Inclusion Criteria: Accepted as kidney recipient Entitlement to the Mexican Institute of Social Security Recipients Exclusion Criteria: Patients who dropped out from study or withdrew the informed consent Insufficient kidney biopsy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Clotilde Fuentes-Orozco, PhD
Organizational Affiliation
Instituto Mexicano del Seguro Social
Official's Role
Principal Investigator
Facility Information:
Facility Name
Western Medical Center, Mexican Institute of Social Security
City
Guadalajara
State/Province
Jalisco
ZIP/Postal Code
44340
Country
Mexico

12. IPD Sharing Statement

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Atorvastatin in the Recipient's Kidney Graft From a Living Donor

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