Use of miRNAs in Growth Hormone Deficiency (GHD)

NCT ID: NCT06455956

Last Updated: 2024-06-13

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

RECRUITING

Total Enrollment

400 participants

Study Classification

OBSERVATIONAL

Study Start Date

2023-04-13

Study Completion Date

2026-03-01

Brief Summary

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This study aims at improving knowledge about the diagnosis of growth hormone deficiency (GHD) and treatment with growth hormone (GH), with the goal of providing information on the presence of new biomarkers, such as miRNAs, for diagnostic and therapeutic purposes, with the goal of establishing a personalized GH treatment scheme, optimizing resources, reducing costs, and improving outcomes.

Detailed Description

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In 200 prepubertal and pubertal subjects with the suspicion of GHD, the levels of three specific circulating miRNas will be measured to establish whether they can be used for the diagnosis of GH deficiency. In subjects with isolated idiopathic GHD (IIGHD), short statured patients born SGA, Noonan and Turner syndromes, and SHOX deficiency, we will also assess the changes of the identified miRNAs before and after 3 months on GH therapy to verify an early growth prediction model for growth response at 12 months on treatment. Finally, we plan to identify any differences in these miRNAs at 3 months on treatment using daily GH versus weekly (long-acting) GH.

Conditions

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Growth Hormone Deficiency

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* Children with short stature and suspicion of GHD
* Subjects with organic GH deficiency


* patients having confirmed GHD enrolled for aim 1
* patients with growth failure and born SGA (\>4 yr of age)
* patients with Noonan and Turner syndrome and growth failure
* patients with short stature homeobox-containing gene deficiency (SHOXD) and growth failure


\- Isolated idiopathic prepubertal naive GHD subjects on long-acting versus daily GH therapy

Exclusion Criteria

-Subjects with underlying genetic conditions and chronic diseases
Minimum Eligible Age

2 Years

Maximum Eligible Age

15 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Azienda Ospedaliera Universitaria Policlinico "G. Martino"

OTHER

Sponsor Role collaborator

Ospedali Riuniti Ancona

OTHER

Sponsor Role collaborator

Federico II University

OTHER

Sponsor Role collaborator

Azienda Unita Sanitaria Locale di Piacenza

OTHER

Sponsor Role collaborator

Azienda Ospedaliero Universitaria Policlinico Modena

OTHER

Sponsor Role collaborator

Azienda USL Reggio Emilia - IRCCS

OTHER_GOV

Sponsor Role collaborator

Azienda Ospedaliero-Universitaria Consorziale Policlinico di Bari

OTHER

Sponsor Role collaborator

Ospedali Riuniti di Foggia

OTHER

Sponsor Role collaborator

IRCCS Ospedale San Raffaele

OTHER

Sponsor Role collaborator

Università degli Studi del Piemonte Orientale Amedeo Avogadro

OTHER

Sponsor Role collaborator

IRCCS Azienda Ospedaliero-Universitaria di Bologna

OTHER

Sponsor Role collaborator

Istituto Auxologico Italiano

OTHER

Sponsor Role collaborator

OSPEDALE CARLO POMA ASST MANTOVA

UNKNOWN

Sponsor Role collaborator

University of Campania Luigi Vanvitelli

OTHER

Sponsor Role collaborator

Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

OTHER

Sponsor Role collaborator

University of Parma

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Maria E Street, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

University of Parma

Locations

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University of Parma

Parma, Emilia-Romagna, Italy

Site Status RECRUITING

Countries

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Italy

Central Contacts

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Maria E Street, MD, PhD

Role: CONTACT

+39 0521 033557

Facility Contacts

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Maria E Street

Role: primary

+39 0521 033557

Other Identifiers

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821/2022/OSS/UNIPR

Identifier Type: -

Identifier Source: org_study_id

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