Autoimmune Blistering Diseases Study

Bullous Pemphigoid Clinical Trial

— AIBD  

Official title:

Prevalence and Clinical Severity of Autoimmune Blistering Diseases

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT02753777
• Other study ID #: 824790
• Status: Recruiting
• Start date: April 2016
• Est. completion date: January 2, 2025

Study information

• Verified date: April 2024
• Source: University of Pennsylvania
• Contact: Victoria P Werth, MD
• Phone: 215-615-2940
• Email: werth[@]pennmedicine.upenn.edu
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 150
• Est. completion date: January 2, 2025
• Est. primary completion date: January 2, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Bullous Pemphigoid
• Pemphigoid, Bullous
• Pemphigus
• Pemphigus Foliaceus
• Pemphigus Vulgaris

Intervention

Other:
• Questionnaires

Locations

Country	Name	City	State
United States	Hospital of the University of Pennsylvania	Philadelphia	Pennsylvania
United States	Hospital of the University of Pennsylvania, Department of Dermatology	Philadelphia	Pennsylvania
United States	University of Pennsylvania, Department of Dermatology	Philadelphia	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
University of Pennsylvania

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Pemphigus Disease Area Index (PDAI)		one year
Primary	Bullous Pemphigoid Disease Area Index (BPDAI)		one year
Secondary	Autoimmune Bullous Disease Quality of Life (ABQOL)		one year
Secondary	Treatment of Autoimmune Bullous Disease Quality of Life (TABQOL)		one year
Secondary	Autoimmune Bullous Skin Disorder Intensity Score (ABSIS)		one year