Establishing the Genetic Profile of Multiple Hereditary Exostoses (HME) in Families of BC

NCT00473850CI-TRIAL-00004690terminatedClinicalTrials.gov clinicaltrialsPublishedExplore in graph →

Why stopped (as posted): This study is recruiting under a different title - "Genotype-Phenotype Correlation of Multiple Hereditary Exostoses: Multicentre Project" NCT00474331

Summary

Brief summary (as posted)

The purpose of this study is to establish the genetic profile of families in British Columbia with HME.

Conditions

Conditions (1)

Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.

Condition (as posted)	Mapped entity	Match	Confidence
Exostoses, Multiple Hereditary	Multiple Osteochondromas	ALIAS	0.90

Interventions

Interventions (0)

Data not yet available

No intervention recorded.

Eligibility

Eligibility (as posted)

Sex: All

Show eligibility criteria text

Inclusion Criteria:

* Diagnosed with HME

References

Publications (0)

Data not yet available

No reference posted for this study.

Registry

Dates and enrollment

Start: Dec 1, 1998
Primary completion: —
Completion: Mar 1, 2023
First posted: May 16, 2007
Last update posted: Apr 15, 2011
Enrollment: 2,000 (estimated)
Lead sponsor: University of British Columbia OTHER
Collaborators: Circle of Care; Vancouver Foundation; Children's & Women's Health Centre of British Columbia
Keywords: DNA sequencing, EXT genes, Hereditary Multiple Exostoses,, also known as Multiple Hereditary Exostoses,, also known as Hereditary Multiple Osteochondromas

Data updated 22 days agoSource updated Apr 15, 2011source: clinicaltrials

Locations

Locations by country (1)

Country	Sites	Recruiting
Canada	1	0

Trial listing is informational. Eligibility is decided by the study team; contact information is on ClinicalTrials.gov.