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Active, not recruiting No phase listed Observational

The PROspera Kidney Transplant ACTIVE Rejection Assessment Registry (ProActive)

ClinicalTrials.gov ID: NCT04091984

Public ClinicalTrials.gov record NCT04091984. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 9:56 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The ProActive registry is a longitudinal, multi-center study with a prospective arm observing clinical care for patients receiving physician ordered Prospera, an allograft rejection test, and a historical control arm collecting data on cases at the same sites whose kidney allograft rejection status was managed with Serum Creatinine SCr/estimated Glomerular Filtration Rate eGFR. This registry will compare patient management and outcomes in patients who receive Prospera (Prospera arm) to the outcomes of the historical control group (control arm) to determine Prospera's clinical utility. High-risk subjects defined as having a biopsy-demonstrated rejection event or at least one pre-existing Donor Specific Antibody DSA with total Mean Fluorescent Intensity MFI\>3000 or a calculated Panel Reactive Antibodies cPRA\>70% will be followed for an additional period up to 24 months in both the Prospera arm and historical control arm.

Study identification

NCT ID
NCT04091984
Recruitment status
Active, not recruiting
Study type
Observational
Phase
Not listed
Lead sponsor
Natera, Inc.
Industry
Enrollment
5,000 participants

Conditions and interventions

Interventions

Diagnostic Test

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 6, 2019 (Actual)
Primary completion
Oct 1, 2026 (Estimated)
Completion
Oct 1, 2027 (Estimated)
Last update posted
Aug 6, 2024

2019 – 2027

United States locations

U.S. sites
55
U.S. states
28
U.S. cities
48
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294 —
Arizona Kidney Disease & Hypertension Centers Phoenix Arizona 85016 —
Arizona Kidney Disease & Hypertension Centers Scottsdale Arizona 85258 —
Arizona Kidney Disease and Hypertension Centers Tucson Arizona 85712 —
Arizona Kidney Disease & Hypertension Centers Tucson Arizona 85718 —
Banner University Medical Center Tucson Arizona 85719 —
University of California Davis Medical Center Davis California 95616 —
University of California, Irvine Irvine California 92697 —
Keck School of Medicine USC Los Angeles California 90033 —
The Regents of the University of California on behalf of its Los Angeles campus Los Angeles California 90095 —
Riverside Community Hospital Riverside California 92501 —
California Institute of Renal Research San Diego California 92123 —
University of Colorado Aurora Colorado 80045 —
Hartford Hospital Hartford Connecticut 06102 —
Yale University, School of Medicine New Haven Connecticut 06520 —
Georgetown University Medical Center Washington D.C. District of Columbia 20057 —
University of Florida Gainesville Florida 32611 —
Florida Health Sciences Center Tampa Florida 33606 —
Cleveland Clinic Florida (Weston) Weston Florida 33331 —
Loyola University Medical Center Maywood Illinois 60153 —
The University of Kansas Medical Center Research Institute Kansas City Kansas 66160 —
University of Maryland Baltimore Maryland 21201 —
Brigham and Women's Hospital Boston Massachusetts 02115 —
Lahey Hospital and Medical Center Burlington Massachusetts 01805 —
Renal Transplant Associates of New England Springfield Massachusetts 01107 —
University of Michigan Ann Arbor Michigan 48109 —
Harper University Hospital, Detroit Medical Center, Wayne State University Detroit Michigan 48201 —
Henry Ford Health System Detroit Michigan 48202 —
St. Louis University St Louis Missouri 63103 —
Washington University School of Medicine in St. Louis St Louis Missouri 63110 —
University of Nebraska Omaha Nebraska 68198 —
University Medical Center of Southern Nevada Las Vegas Nevada 89102 —
Saint Barnabas Medical Center Livingston New Jersey 07039 —
Erie County Medical Center Buffalo New York 14215 —
Northwell Health, Inc Manhasset New York 11030 —
Columbia University Medical Center New York New York 10032 —
The Research Institute at Westchester Medical Center Valhalla New York 10595 —
East Carolina University Greenville North Carolina 27858 —
Wake Forest University Health Sciences Winston-Salem North Carolina 27157 —
The Cleveland Clinic Foundation Cleveland Ohio 44195 —
The University of Toledo Toledo Ohio 43606 —
Legacy Research Portland Oregon 97232 —
Lehigh Valley Health Network Allentown Pennsylvania 18103 —
Kidney Care Specialists Bethlehem Pennsylvania 18017 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
Einstein Medical Center Philadelphia Pennsylvania 19141 —
Rhode Island Hospital Providence Rhode Island 02903 —
Vanderbilt University Nashville Tennessee 37235 —
UT Southwestern Dallas Texas 75390 —
Baylor Scott and White Research Institute Temple Texas 76508 —
IHC Health Services, Inc Salt Lake City Utah 84111 —
University of Utah Salt Lake City Utah 84132 —
Virginia Commonwealth University Richmond Virginia 23298 —
University of Washington Seattle Washington 98195 —
West Virginia University Morgantown West Virginia 26506 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04091984, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 6, 2024 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04091984 live on ClinicalTrials.gov.

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