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Genotype-phenotype Correlation in Junctional Epidermolysis Bullosa

NCT04727268 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2021-10-04

No results posted yet for this study

Summary

This study will collect genetic and clinical information of junctional epidermolysis bullosa (JEB) patients. Computer analysis will be performed on genetic mutations found in these patients and this will be correlated with their clinical characteristics.

Conditions

  • Junctional Epidermolysis Bullosa
  • Laryngo Onycho Cutaneous Syndrome

Interventions

OTHER

No intervention

No interventions present in this study.

Sponsors & Collaborators

  • Dystrophic Epidermolysis Bullosa Research Association (DEBRA)

    collaborator UNKNOWN

  • University of Birmingham

    collaborator OTHER

  • University Hospital Birmingham NHS Foundation Trust

    lead OTHER

Eligibility

Min Age
0 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2021-09-27
Primary Completion
2021-12-30
Completion
2021-12-30

Countries

  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04727268 on ClinicalTrials.gov