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Translation of a Diagnostic Test for Lupus Flare Prediction From Bench to Clinic

Translation of a Diagnostic Test for Lupus Flare Prediction From Bench to Clinic

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04018222
Acronym
TOTAL FEEDBACK
Enrollment
60
Registered
2019-07-12
Start date
2019-05-31
Completion date
2020-12-31
Last updated
2020-09-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Lupus Erythematosus, Lupus Flare, SLE, System; Lupus Erythematosus

Keywords

Systemic Lupus Erythematosus, SLE, Lupus Flare, Flare Prediction, Lupus

Brief summary

This study is investigating the development of a diagnostic test intended to predict flares in patients with Systemic Lupus Erythematosus. Over a six-month period, the participant will donate blood samples for researchers to evaluate the types of proteins that are in their blood. During this time the participant will also visit a research physician to undergo a physical exam that will include an evaluation of the disease's level of activity. Questionnaires will be answered too, either via email, phone call, or a research app for android and iPhone devices. During this six-month period, if the participant experiences a lupus flare, they are strongly encouraged to visit the research physician to receive a complimentary medical evaluation.

Detailed description

The purpose of this study is to further validate an algorithm used in a lupus flare-prediction that has been developed. The investigators will be looking at different proteins in the blood that are commonly associated with lupus flares and could warn of the risk of a future flare. Participation in this study will involve three separate visits with a research physician for six months. These will proceed as a baseline visit, a three-month visit, and a six-month visit. During each of these visits the physician assesses the participant's physical condition and take blood samples for both research and medical purposes. Throughout this study, the participant will also complete a series of questionnaires to assess their wellness and day-to-day challenges. After the initial visit, the participant will be contacted to complete a monthly survey that evaluates if there have been any changes in your condition. This survey can be completed either via email, a phone call discussion, or the study's unique research app. Three of these six surveys will be completed during the physician's visit, however, the other three will be completed in the preferred medium. Throughout the six-month period while you are on this study, if at any point the participant experiences a flare, they are encouraged to visit the research physician. During this visit, they will receive a physician's evaluation to ensure your medical condition and collect blood samples for our research at no cost to the participant.

Interventions

None listed

Sponsors

Oklahoma Center for the Advancement of Science and Technology
CollaboratorOTHER
Progentec Diagnostics, Inc.
Lead SponsorINDUSTRY

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

Lupus Patients * Females or males age 18 or older * Meet ≥ 4 American College of Rheumatology (ACR) classification criteria for SLE, by medical record review and/or clinical/laboratory assessment OR * Meet ≥ 4 Systemic Lupus Collaborating Clinic (SLICC) classification for SLE, including at least one clinical and one immunologic criterion, by medical record review and/or clinical/laboratory assessment OR * Meet SLE classification by SLICC with ANA positivity * Have a clinical diagnosis of active SLE, per physician assessment * Have the ability to understand the requirements of the study, provide written informed consent including consent for the use and disclosure of research-related health information, and comply with the study data collection procedures Healthy Controls * Matched to a currently-enrolled patient that is self-reported race, gender, and current age within 5 years. * No medical history of rheumatological or auto-immune diseases.

Exclusion criteria

* Active diagnosis of Lupus Nephritis * Inability to comply with the study data collection procedures * Currently being treated with cyclophosphamide * Treated with rituximab within the last six months * Currently being treated with an investigational drug * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
SLEDAIBaseline Physician VisitSystemic Lupus Erythematosus Disease Activity Index - measures the patient's disease activity through clinical and laboratory values

Secondary

MeasureTime frameDescription
SF-36Baseline at Physician VisitShort Form 36 Questions. General Wellness measurement

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026