Β3-adrenoreceptor As Prognostic Marker in Neuroblastoma and Ewing Sarcoma

NCT ID: NCT06851221

Last Updated: 2025-02-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

95 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-08-05

Study Completion Date

2024-03-05

Brief Summary

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This study on biological samples of patients affected by neuroblastoma and Ewing sarcoma aims at validating the beta3-adrenoreceptor as prognostic biomarker.

Detailed Description

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Conditions

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Neuroblastoma Ewing Sarcoma

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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biological samples analysis

Group Type OTHER

beta3 expression

Intervention Type DIAGNOSTIC_TEST

the samples leftover from the standard diagnostic procedures will be analyzed for the expression of the beta3-adrenoreceptor

Interventions

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beta3 expression

the samples leftover from the standard diagnostic procedures will be analyzed for the expression of the beta3-adrenoreceptor

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

* diagnosis of Ewing sarcoma or neuroblastoma

Exclusion Criteria

* sieropositivity
Minimum Eligible Age

0 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Meyer Children's Hospital IRCCS

OTHER

Sponsor Role lead

Responsible Party

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Maura Calvani

Head of Traslational oncoematology laboratory

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Laboratorio traslazionale in oncoematologia

Florence, Italy, Italy

Site Status

Countries

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Italy

Other Identifiers

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BETA3TumPed

Identifier Type: -

Identifier Source: org_study_id

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