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NCT02945345 · ClinicalTrials.gov registry record

Clinical Responsiveness of Dermatomyositis Using Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI)

A clinical trial of Dermatomyositis, sponsored by University of Pennsylvania.

Recruiting
Registry status
300
Enrollment target
1
Study location

NCT02945345 is a study of Dermatomyositis that is actively recruiting participants, run by University of Pennsylvania. The registered enrollment target is 300 participants, below the 469-participant average among 19 other Dermatomyositis trials with a reported enrollment target (36% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT02945345, a study of Dermatomyositis, is actively recruiting participants, sponsored by University of Pennsylvania.

RECRUITING
Registry status
300 participants
Enrollment target
1
Study location

Study Summary

The Evaluation of Clinical Responsiveness Using the Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI), established in 2008, is a one-site database study conducted at the University of Pennsylvania. The database has yielded valuable information and clinical insights into the pathophysiology, disease processes, including psychological responses, treatments and quality of life associated with dermatomyositis. The CDASI database incorporates the Cutaneous Dermatomyositis Disease Area and Severity Index), a validated outcome measure of disease responsiveness in patients, and other assessment tools, surveys and patient information to help validate the clinical course and quality of life of patients with dermatomyositis. The CDASI database has led to publication of comparison studies of CDASI and other clinical instruments and the effect of dermatomyositis on Quality of Life (QoL). The CDASI database is an ongoing resource that enables clinicians to evaluate the evolving clinical changes, treatment modalities and patient response to a challenging disease. Data will be analysed over a 5 years.

Conditions Studied

Study Locations (1)

Pennsylvania

  • Hospital of the University of Pennsylvania - Philadelphia

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2008-06
Est. Completion 2030-01-02

Sponsor

University of Pennsylvania

1,423 total trials

What the Registry Record Tells You About NCT02945345

The ClinicalTrials.gov registry entry for NCT02945345 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 469-participant average among 19 other Dermatomyositis trials with a reported enrollment target (36% lower). The listed sponsor is University of Pennsylvania, which has 1,423 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Dermatomyositis appearing as the primary indexed condition, and to 0 interventions.

NCT02945345 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT02945345 about?

NCT02945345 is a clinical study titled "Clinical Responsiveness of Dermatomyositis Using Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI)". The Evaluation of Clinical Responsiveness Using the Cutaneous Dermatomyositis Disease Area and Severity Index (CDASI), established in 2008, is a one-site database study conducted at the University of Pennsylvania. The database has yielded valuable information and clinical insights into the pathophys...

What is the current status of trial NCT02945345?

This trial is currently recruiting. The enrollment target is 300 participants. The study started on 2008-06. Estimated completion is 2030-01-02.

What conditions does trial NCT02945345 study?

This clinical trial studies the following conditions: Dermatomyositis.

Who is sponsoring clinical trial NCT02945345?

This trial is sponsored by University of Pennsylvania, which has 1,423 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02945345 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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