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OpenTrials
Completed

NCT Number: NCT02178969

Short Term Observational Study in DEB Patients

The purpose of this study is to better understand disease extent and to identify appropriate methodologies to evaluate (dystrophic epidermolysis bullosa) DEB in a quantitative and qualitative manner.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Written informed consent is provided. Patients 18 years of age and older, and parent(s)/legal guardian(s) of patients younger than 18 years of age, must provide written informed consent prior to participating in the study; additionally, informed assent will be obtained from patients younger than 18 years of age as specified by local requirements.
  • Patient must have a documented diagnosis of DEB based on genetic analysis showing a mutation in COL7A1 or, in the opinion of the investigator, a confirmed diagnosis of DEB based on histologic criteria (antigen mapping or electron microscopy).
  • Patient must have at least 5 wounds that are suitable for imaging, in the opinion of the investigator, at the time of enrollment.
  • Patient is willing and able to undergo the protocol-specified procedures.

Exclusion criteria

  • Patient has used or is currently using experimental treatment for DEB including, but not limited to, bone marrow transplantation, systemic immune suppression, or experimental procedures that involve live cells, with potential for systemic spread such as gene transfer, stem cell infusions, or other cell type injections such that, in the opinion of the investigator, inclusion poses an unacceptable risk to the patient or interpretation of these study data.
  • Patient has squamous cell carcinoma with evidence of locally invasive disease or distant metastases.
  • Patient is pregnant.

Treatment and study plan

Primary outcomes

  1. Wound Surface Area (WSA) of patient- and investigator-selected wounds

    Time frame: Over 4 weeks

  2. Wound Surface Area (WSA) as a percentage of Body Surface Area (BSA) in patients with DEB

    Time frame: Over 4 weeks

Secondary outcomes

  1. The number, severity and relationship to study procedures of adverse events (AEs) and serious AEs (SAEs)

    Time frame: Over 4 weeks

Sponsors and collaborators

Lead sponsor

Shire

Industry

Registry information

Official study title

A Prospective Short-term Study to Evaluate Methodologies for the Assessment of Disease Extent, Impact, and Wound Evolution in Patients With Dystrophic Epidermolysis Bullosa (DEB)

Important dates

Study start
2014
Primary completion
2015
Study completion
2015
First posted
Jul 1, 2014
Registry last updated
Mar 17, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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