Height, Ulnar Length and Forearm Function in Multiple Hereditary Exostoses
NCT ID: NCT05914298
Last Updated: 2023-06-22
Study Results
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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COMPLETED
408 participants
OBSERVATIONAL
2018-01-01
2022-02-01
Brief Summary
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Detailed Description
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The involvement of upper-limb bones by HME is associated with greater loss of function than elsewhere in the body, but even here the loss of function may be limited. Moreover, the constant relationship between height and ulnar length has long been recognized in forensic medicine and has been recently analyzed also in HME, in order to predict the clinical and functional outcomes of the upper limb.
the present registry aims to collect demographic, clinical, functional and radiographic information from patients with HME in order to establish phenotypic predictors of severity of the disease and potential association with genotypic patterns
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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HME group
204 children and adult patients with HME, admitted to our Hospital for diagnosis and treatment.
the patients will be stratified by age in four subgroups:
* subgroup I (0-7 Years)
* subgroup II (8-12 Years)
* subgroup III (13-18 Years)
* subgroup IV (\>18 Years)
blood and buccal swab genetic test
blood samples and buccal swabs will be obtained from patients with HME in order to analyze the genotype (EXT1 or EXT2 mutations) and correlate the genotypic pattern with the phenotypic presentation
PUL
measurement of ulnar length with anthropometer and patient's height
Range of motion
measurement of range of motion of elbow, forearm and wrist
healty control group
204 children and adult voluntary healty controls will be stratified in the same manner and matched with the population in study in order to assess normal and pathologic growth.
PUL
measurement of ulnar length with anthropometer and patient's height
Range of motion
measurement of range of motion of elbow, forearm and wrist
Interventions
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blood and buccal swab genetic test
blood samples and buccal swabs will be obtained from patients with HME in order to analyze the genotype (EXT1 or EXT2 mutations) and correlate the genotypic pattern with the phenotypic presentation
PUL
measurement of ulnar length with anthropometer and patient's height
Range of motion
measurement of range of motion of elbow, forearm and wrist
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Patients, adults or minors, who are unable to give their timely informed consent.
ALL
Yes
Sponsors
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Istituto Ortopedico Rizzoli
OTHER
Responsible Party
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Principal Investigators
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Giovanni Luigi Di Gennaro, MD
Role: PRINCIPAL_INVESTIGATOR
Istituto Ortopedico Rizzoli
Locations
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Manila Boarini
Bologna, , Italy
Countries
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References
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Pedrini E, De Luca A, Valente EM, Maini V, Capponcelli S, Mordenti M, Mingarelli R, Sangiorgi L, Dallapiccola B. Novel EXT1 and EXT2 mutations identified by DHPLC in Italian patients with multiple osteochondromas. Hum Mutat. 2005 Sep;26(3):280. doi: 10.1002/humu.9359.
Mordenti M, Ferrari E, Pedrini E, Fabbri N, Campanacci L, Muselli M, Sangiorgi L. Validation of a new multiple osteochondromas classification through Switching Neural Networks. Am J Med Genet A. 2013 Mar;161A(3):556-60. doi: 10.1002/ajmg.a.35819. Epub 2013 Feb 8.
Pedrini E, Jennes I, Tremosini M, Milanesi A, Mordenti M, Parra A, Sgariglia F, Zuntini M, Campanacci L, Fabbri N, Pignotti E, Wuyts W, Sangiorgi L. Genotype-phenotype correlation study in 529 patients with multiple hereditary exostoses: identification of "protective" and "risk" factors. J Bone Joint Surg Am. 2011 Dec 21;93(24):2294-302. doi: 10.2106/JBJS.J.00949.
Clement ND, Porter DE. Forearm deformity in patients with hereditary multiple exostoses: factors associated with range of motion and radial head dislocation. J Bone Joint Surg Am. 2013 Sep 4;95(17):1586-92. doi: 10.2106/JBJS.L.00736.
Other Identifiers
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0012479
Identifier Type: -
Identifier Source: org_study_id
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