Exostoses, Multiple Hereditary: Clinical Trials

12 trials for Exostoses, Multiple Hereditary, newest first

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6 completed, 3 recruiting, 2 terminated, 1 suspended. 1 Not applicable, 1 Phase 2.

By phase and status

PhaseTrialsStatus
Not applicable1Completed 1
Phase 21Terminated 1

Follow Exostoses, Multiple Hereditary: new trials by email Literature Review of Exostoses, Multiple Hereditary trials Research Report on Exostoses, Multiple Hereditary

Trials newest first · largest first

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
Survey on Multiple Osteochondromas and Enchondromatoses During the Transition From Paediatric Care to Adult Care
Multiple Osteochondroma, Enchondromatosis
CompletedIstituto Ortopedico Rizzoli912025-11-242026-09-24
Descriptive Analysis of Surgeries in Patients With Multiple Osteochondromas
Surgery for osteochondromas - Multiple Osteochondroma
RecruitingIstituto Ortopedico Rizzoli3002025-10-232026-05-15
Functional and Morphological Characterization of Multiple Osteochondromas Disorder
Hereditary Multiple Osteochondromas
RecruitingIstituto Ortopedico Rizzoli602025-05-212026-03-24
Ready to Sail: Evaluating Sailing's Feasibility as Ergotherapy
5-day sailing activity - Multiple Osteochondroma, Ollier Disease
Not applicableCompletedIstituto Ortopedico Rizzoli82024-05-162025-03-21
Resilience and Coping in a Rare Skeletal Disease Population to Face Coronavirus (COVID-19) Outbreak Distress: a Longitudinal Study
Multiple Osteochondroma, Osteogenesis Imperfecta
CompletedIstituto Ortopedico Rizzoli152021-05-122023-03-01
An Efficacy and Safety Study of Palovarotene for the Treatment of MO
Palovarotene 2.5 mg, Palovarotene 5.0 mg, Placebo - Exostoses, Multiple Hereditary
Phase 2TerminatedClementia Pharmaceuticals Inc.1932018-03-222022-08-01
Height, Ulnar Length and Forearm Function in Multiple Hereditary Exostoses
blood and buccal swab genetic test, PUL, Range of motion - Exostoses, Multiple Hereditary
CompletedIstituto Ortopedico Rizzoli4082018-01-012023-06-22
NGS Strategy Effectiveness in Molecular Diagnosis
NGS molecular screening - Multiple Osteochondroma, Osteogenesis Imperfecta
CompletedIstituto Ortopedico Rizzoli4002014-09-292018-06-18
Registry of Multiple Osteochondromas
Multiple Osteochondromas
RecruitingLuca Sangiorgi100002013-06-282025-11-20
The Health-Related Quality of Life in Patients With Hereditary Multiple Exostoses
Exostoses, Multiple Hereditary
CompletedUniversity of British Columbia2002007-05-012022-05-18
Gene Mutations and Orthopaedic Symptoms Correlation of Multiple Hereditary Exostoses: Multicentre Project
Exostoses, Multiple Hereditary
SuspendedUniversity of British Columbia20002004-06-012022-05-18
Establishing the Genetic Profile of Multiple Hereditary Exostoses (HME) in Families of BC
Exostoses, Multiple Hereditary
TerminatedUniversity of British Columbia20001998-12-012011-04-15

Narrower conditions

Enchondromatosis (3)  ·  Osteogenesis Imperfecta (3)  ·  Rare Diseases (2)  ·  COVID-19 (1)  ·  Osteochondroma (1)  ·  Psychological Well-Being (1)

Broader conditions

Bone Diseases (12)  ·  Bone Diseases, Developmental (12)  ·  Congenital, Hereditary, and Neonatal Diseases and Abnormalities (12)  ·  Exostoses (12)  ·  Genetic Diseases, Inborn (12)  ·  Hyperostosis (12)  ·  Musculoskeletal Diseases (12)  ·  Neoplasms (12)  ·  Neoplasms by Histologic Type (12)  ·  Neoplasms, Bone Tissue (12)  ·  Neoplasms, Connective Tissue (12)  ·  Neoplasms, Connective and Soft Tissue (12)  ·  Neoplastic Syndromes, Hereditary (12)  ·  Osteochondrodysplasias (12)  ·  Osteochondromatosis (12)

Interventions

Blood Specimen Collection (1)  ·  Palovarotene (1)  ·  Range of Motion, Articular (1)  ·  Surgical Procedures, Operative (1)

Sponsors

Istituto Ortopedico Rizzoli (7)  ·  University of British Columbia (3)  ·  Clementia Pharmaceuticals Inc. (1)  ·  Luca Sangiorgi (1)

Countries

Italy (8)  ·  Canada (4)  ·  Australia (1)  ·  Belgium (1)  ·  France (1)  ·  Japan (1)  ·  Netherlands (1)  ·  Portugal (1)  ·  Spain (1)  ·  Turkey (Türkiye) (1)  ·  United Kingdom (1)  ·  United States (1)

Top investigators

Christine Alvarez, MD (3)  ·  Giovanni Luigi Di Gennaro, MD (1)  ·  Luca Sangiorgi, MD, PhD (1)  ·  Luca Sangiorgi, MD, PhD, MS (1)  ·  Luca Sangiorgi, MD, Phd (1)

Results publications

PMID 16088908, PMID 22258776, PMID 23401177, PMID 24005199, PMID 41131085, PMID 41188357

NIH funding

2017 (1)