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ReclutandoNCT04571658Registro de ClinicalTrials.gov

NEPTUNE Match Study

Nephrotic Syndrome in Children · Focal Segmental Glomerulosclerosis · Minimal Change Disease · Minimal Change Nephrotic Syndrome · Membranous Nephropathy · FSGS · MCD · MCD - Minimal Change Disease · Alport Syndrome

LO ESENCIAL

De qué trata este estudio

El registro indica que este estudio recluta participantes. La disponibilidad puede variar por centro.

Tipo de estudio
De intervención
Fase
No aplica
Rango de edad
1 años - 80 años
Sexo admitido
Todos los sexos
Voluntarios sanos
No aceptados
Participantes
375 Estimado

Estos son puntos de partida, no una decisión de elegibilidad. El equipo debe revisar todos los requisitos.

Las explicaciones y la navegación están en español. Los textos proporcionados por el registro, incluidos títulos, resúmenes y criterios, se conservan en su idioma original. Puedes pedir orientación en español a WCR.

Acerca de la investigación

NEPTUNE Match is an additional opportunity offered to NEPTUNE study participants to prospectively recruit and communicate patient-specific clinical trial matching with kidney patients and their physician investigators.

Leer la descripción completa

This is a prospective, open-label study testing the ability to effectively communicate patient-specific clinical trial matching with kidney patients and clinician investigators. The study consists of four components:

1. Recruitment of participants from the NEPTUNE observational cohort study
2. Generation of participant profile-trial match assessment using data from the NEPTUNE observational study and profiling units by the NEPTUNE Molecular Nephrology Board
3. Establishing and testing a framework to communicate disease-trial drug mechanism matching with investigators and patients
4. Retrospective comparison of kidney health outcomes in subjects enrolled in trials that aligned with their match vs. trial subjects with mis-aligned or unknown match alignment.

¿Quién podría participar?

La lista siguiente contiene el texto del patrocinador. Puede incluir condiciones, tratamientos previos, resultados de pruebas y otros requisitos. Aparecer en tu búsqueda no significa que califiques.

Inclusion Criteria:

1. Consented and eligible participants in the biopsied or non-biopsied cohorts of the NEPTUNE observational study
2. Must be potentially eligible for the NEPTUNE Match partnering trials (e.g. if no trial is enrolling a participant under age 6, those under 6 are not eligible).

Note: NEPTUNE Match partnering trials and associated eligibility criteria are expected to be dynamic and change as trial protocols are developed, activated, and amended.
3. Regular nephrology healthcare provided at a NEPTUNE study site.
4. Willing and able to consent, and as appropriate assent, to participate in NEPTUNE Match

Exclusion Criteria:

Currently non-NEPTUNE observational study participants are not eligible to be matched to a clinical trial using these biomarker assessments.

Exclusion Criteria:

1\. Non-English or non-Spanish speaking

Entiende la evaluación inicial

Tratamiento, grupos y participación

El registro puede describir tratamientos y duración sin incluir un calendario completo. Pide al equipo las visitas, procedimientos, riesgos, costos y alternativas. Mantén tu atención habitual salvo que tu médico te indique un cambio.

Asignación
No aplica
Enmascaramiento
Sin enmascaramiento
NEPTUNE Match Participants

Approximately 375 participants will be consented from the NEPTUNE observational study with age and demographic groups representing the patient population in the NEPTUNE study site geographical areas.

NEPTUNE observational cohort eligibility includes: participants in NEPTUNE observational cohort A are of any age and have a biopsy-confirmed diagnosis of Focal Segmental Glomerulosclerosis (FSGS), Minimal Change Disease (MCD), or Membranous Nephropathy (MN). Participants in NEPTUNE observational cohort B have documented NS based on proteinuria, serum albumin, and/or edema with age of onset less than 19 years.

Other: Communication

Communication OTHER

The NEPTUNE Match study includes an interdisciplinary Communication Team that will translate findings from the Molecular Nephrology Board (MNB) to inform patients of the matching assessment with ongoing clinical trials. This team has considerable experience with conveying complex biomedical research information to patients and families and includes experts in precision nephrology, nephrology patient \[adult and pediatric\] communication, and health education.

Prepara tus preguntas

Qué evalúan los investigadores

Estas medidas indican qué se estudia. No prueban que un tratamiento funcione.

Medidas principales

Matched participants with at least one clinical trial receive a MNB assessment

Plazo: 0-4 weeks

Proportion of NEPTUNE Match participants with at least one matching clinical trial, defined as receiving a Molecular Nephrology Board (MNB) assessment that provides a match to at least one targeted therapy in an ongoing clinical trial

Efficacy of communication methods at time of communication visit, measured by Teach Back 1 summary score

Plazo: 12 weeks

Key findings from MNB trial matching analyses and deliberations will be conveyed to study participants using a NEPTUNE Match Report that summarizes the findings. The report indicates the strength of matching to ongoing clinical trials and the uncertainty and research origins of the information. A sample Match Report can be found in Appendix C. The report will not contain individual data elements reviewed by the MNB. The creation of NEPTUNE Match Reports will follow health education principles including matching of content to patients' informational needs and health literacy levels, use of visual aids to clarify meaning of information, and avoidance of information overload of the participant.

Kidney health endpoints that are specific to each individual trial

Plazo: 0-60 months

The analytic integration supporting the Molecular Nephrology Board (MNB) case review will be initiated and will occur. The MNB will conduct the discussion and generate the integrated data summary and case report inclusive of clinical trial matching by webinar. Input from the MNB will be used to generate a final version of the participant NEPTUNE Match Report. This is a longitudinal outcome that will be assessed at the end of the study relative to endpoints specific to matched clinical trials, assessing the superiority of stratification (matching or alignment of patient molecular profiles to targeted therapies in clinical trials) to non-stratification.

Medidas secundarias

Efficacy of communication methods at follow up, measured by Teach Back of key concepts

Plazo: 14-18 weeks

3 defined teachback concepts will be scored to indicate the participant's understanding of strength of matching.

Psychological distress measured by the STAI assessment

Plazo: 14-18 weeks

State Trait Anxiety Inventory (mini-STAI) scale will be used to assess a participant's psychological distress around their participation in NEPTUNE Match at the consent visit and the follow up visit.

Psychological distress measured by the FACToR-NEPTUNE assessment

Plazo: 14-18 weeks

FACToR-NEPTUNE is a measure that has been modified from the Feelings About genomiC Testing Results (FACToR). FACToR-12 is used to assess the psychosocial impact of returning genomic findings to patients in research and clinical practice. In the FACToR-NEPTUNE assessment the measure will assess the psychosocial impact after receiving the NEPTUNE Match Report.

El registro no indica resultados publicados.

Revisa las tablas completas y sus limitaciones en el registro oficial.

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Centros de investigación (16)

El estado general puede diferir del estado de un centro. Confirma la disponibilidad antes de trasladarte.

16 centros

Emory University Hospital - Children's Hospital of AtlantaAtlanta, Georgia, United StatesReclutando
Emily YunCONTACTemily.yun@emory.edu
Laurence Greenbaum, MD, PhDPRINCIPAL_INVESTIGATOR
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John H. Stroger, Jr., Hospital of Cook CountyChicago, Illinois, United StatesReclutando
University of Kansas Medical CenterKansas City, Kansas, United StatesReclutando
Catherine CreedCONTACTccreed@kumc.edu
Ellen McCarthy, MDPRINCIPAL_INVESTIGATOR
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Johns Hopkins MedicineBaltimore, Maryland, United StatesReclutando
MIahje WilliamsCONTACTmwil296@jhmi.edu
Meredith Adkinson, MDPRINCIPAL_INVESTIGATOR
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University of MichiganAnn Arbor, Michigan, United StatesPor invitación
Children's Mercy HospitalKansas City, Missouri, United StatesReclutando
Kelsey MarkusCONTACTkemarkus@cmh.edu
Tarak Srivastava, MDPRINCIPAL_INVESTIGATOR
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Northwell/Cohen's Children's HospitalNew Hyde Park, New York, United StatesReclutando
Suzanne Vento, BSNCONTACTsvento@northwell.edu
Christine Sethna, MD, MSPRINCIPAL_INVESTIGATOR
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Columbia University Medical CenterNew York, New York, United StatesReclutando
Anup PradhanCONTACT
Pietro Canetta, MDPRINCIPAL_INVESTIGATOR
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University of North Carolina Chapel HillChapel Hill, North Carolina, United StatesReclutando
Anne FromentCONTACTanne_froment@med.unc.edu
Maria Fernanda Ochoa ToroCONTACTferochoc@email.unc.edu
Vimal Derebail, MD, MSPRINCIPAL_INVESTIGATOR
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Cleveland Clinic FoundationCleveland, Ohio, United StatesReclutando
Stefanie LarsonCONTACTlarsons2@ccf.org
Katherine Dell, MDPRINCIPAL_INVESTIGATOR
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Hospital of the University of PennsylvaniaPhiladelphia, Pennsylvania, United StatesReclutando
Krishna Kallem, MSCONTACTKrishna.Kallem@pennmedicine.upenn.edu
Larry Holzman, MDPRINCIPAL_INVESTIGATOR
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Temple UniversityPhiladelphia, Pennsylvania, United StatesReclutando
Zoe PfefferCONTACTzoe.pfeffer@tuhs.temple.edu
Iris Lee, MDPRINCIPAL_INVESTIGATOR
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Medical University of South CarolinaCharlotte, South Carolina, United StatesReclutando
David Selewski, MD, MSPRINCIPAL_INVESTIGATOR
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Seattle Children's HospitalSeattle, Washington, United StatesReclutando
Sangeeta Hingorani, MDPRINCIPAL_INVESTIGATOR
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University of Washington Medical CenterSeattle, Washington, United StatesReclutando
Linda Manahan, BSNCONTACTlmanahan@nephrology.washington.edu
Ashley Jefferson, MDPRINCIPAL_INVESTIGATOR
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Providence Sacred Heart Medical CenterSpokane, Washington, United StatesReclutando
Kelli KuykendallCONTACTkelli.kuykendall@providence.org
Katherine Tuttle, MDPRINCIPAL_INVESTIGATOR
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Equipo y fechas

Patrocinador principal
University of Michigan
Inicio del estudio
2 may 2022 Real
Finalización primaria
30 dic 2029 Estimado
Finalización del estudio
30 dic 2029 Estimado
Primera publicación
1 oct 2020 Real
Última actualización
10 nov 2026 Real

Contactos oficiales del estudio

Hailey E Desmond, MSCONTACTheturner@med.umich.edu734-232-4851
Chrysta C Lienczewski, BSCONTACTboridley@med.umich.edu734-615-5021
Título oficial del estudio

Implementing Precision Medicine for Glomerular Diseases in the Nephrotic Syndrome Study Network (NEPTUNE)

EL PRÓXIMO PASO, CON APOYO HUMANO

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Fuente: API v2 de ClinicalTrials.gov. Patrocinadores e investigadores envían la información. La NLM no aprueba la seguridad ni la ciencia de todos los estudios registrados. Aviso del registro.

Consultado: 11 nov 2026 · Última actualización del registro: 10 nov 2026