NCT Number: NCT02753777
Autoimmune Blistering Diseases Study
Pemphigus and bullous pemphigoid (BP) are severe autoimmune blistering diseases (AIBD) that pose a critical need for new therapeutic approaches. Clinical trials in pemphigus and BP will require the availability of validated disease severity measures that can be used to define primary outcomes.
Interested in participating?
Request InfoKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Primary location
Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania, United States
About this study
The disease severity instruments for pemphigus and BP, the Pemphigus Disease Area Index (PDAI) and the Bullous Pemphigoid Disease Area Index (BPDAI), respectively, have the potential to capture changes in all grades of disease activity, including mild disease, and therefore represent a substantial improvement over simple lesion counts or measurements of affected body surface area. However, full validation of the PDAI and BPDAI for use in clinical trials will require additional and more extensive measurements that will enable us to classify patients correctly by disease severity and be able to define the minimal change in score that is clinically significant.
This database study will compare the Pemphigus Disease Area and Severity Index (PDAI) and the Bullous Pemphigoid Disease Area Index (BPDAI) against other disease severity measures, including the Autoimmune Bullous Skin Disorder Intensity Score (ABSIS) and a physician's global assessment. Additionally, patients will be asked to rate their overall disease severity using a visual analogue scale, the patient's global assessment. Participants will also have the option to donate blood samples to our AIBD blood bank for immunologic and pathophysiologic studies.
The purpose of this database study will also be to evaluate quality of life (QoL) measures and correlate these QoL measures with disease severity in patients with pemphigus and BP. QoL is an important and independent component of disease impact on patients. This database study will use the following QoL measures: the SF-36, which is a nonspecific QoL measure; the Skindez-29 and the Dermatology Life Quality Index (DLQI), which are dermatology-specific instruments; the Autoimmune Bullous Disease Quality of Life (ABQOL) and Treatment of Autoimmune Bullous Disease Quality of Life (TABQOL) questionnaires, which are AIBD-specific tools. The results will be utilized in planning future clinical studies.
The AIBD study will be conducted only at Penn at this time. Data from the study will be entered into a password protected, web-based database that is used only at Penn.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Gender/Age: Males or females above 18 years old
- Diagnosis: pemphigus vulgaris, pemphigus foliaceus, bullous pemphigoid
- Subjects able to give informed consent
Exclusion criteria
- Patients who are under age 18 years.
- Patients without pemphigus or pemphigoid diseases
- Penn employees
- Penn students
- Cognitively impaired persons
Treatment and study plan
Primary outcomes
-
Pemphigus Disease Area Index (PDAI)
Time frame: one year
-
Bullous Pemphigoid Disease Area Index (BPDAI)
Time frame: one year
Secondary outcomes
-
Autoimmune Bullous Disease Quality of Life (ABQOL)
Time frame: one year
-
Treatment of Autoimmune Bullous Disease Quality of Life (TABQOL)
Time frame: one year
-
Autoimmune Bullous Skin Disorder Intensity Score (ABSIS)
Time frame: one year
Study contacts
Contact information is provided by the study sponsor or research team.
Joyce Okawa, RN
CONTACT
Victoria P Werth, MD
CONTACT
Sponsors and collaborators
Lead sponsor
University of Pennsylvania
Other
Registry information
Official study title
Prevalence and Clinical Severity of Autoimmune Blistering Diseases
Acronym: AIBD
Important dates
- Study start
- 2016
- Primary completion
- 2030
- Study completion
- 2030
- First posted
- Apr 28, 2016
- Registry last updated
- Mar 30, 2026
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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