Morphea in Adults and Children (MAC) Cohort Study: A Morphea Registry and DNA Repository
University of Texas Southwestern Medical Center · NCT01808937
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Up to age 90 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Observational
- Target enrollment
- 500
- US sites recruiting
- 1
- Study start
- May 2007
- Record last updated
- May 12, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The Morphea in Adults and Children (MAC) cohort is the first registry for both children and adults with morphea (also known as localized scleroderma) in the country. The purpose of the registry is to learn more about morphea, specifically:
- How morphea behaves over time
- How frequently specific problems occur along with morphea (for example, arthritis)
- Whether morphea has an autoimmune background
Being studied: Morphea
Conditions: Scleroderma, Localized; Morphea; Frontal Linear Scleroderma en Coup de Sabre; Scleroderma, Circumscribed; Scleroderma, Linear
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Patient must have a clinical diagnosis of morphea confirmed by the primary investigator and by histopathological examination.
- Ages 0-90 years old
- Children must weigh more than 20 lbs. in order to satisfy Children's Medical Center policy for the maximum amount of blood drawn in a 24 hour period.
- Patient or legal guardian must be able to speak and read at a 6th grade reading level.
- Both male and female patients will be eligible
- All races and ethnic backgrounds will be included
- Relationships to proband: All patients with morphea will be included. A patient's family history will be reviewed and if there is a family history of morphea or systemic sclerosis then we will give the study patient the investigator's contact information and ask the family member to call the study team to answer any questions and enroll them in the study if they choose to do so.
- Ability to give informed consent: Patients must be able to give informed consent or they will give assent with parent or guardian consent as a minor to be a part of the morphea registry.
Exclusion Criteria
- Patients who have been coded as morphea (701.0), but do not have morphea/localized scleroderma (examples: steroid atrophy, acquired keratoderma, keloids, nephrogenic fibrosing dermopathy, systemic sclerosis, lichen sclerosis)
Recruiting US locations
UT Southwestern Medical Center - Department of Dermatology
Dallas, TX 75390-9069
Site contact: Heidi Jacobe, MD, MSCS · 214.633.1837 · heidi.jacobe@utsouthwestern.edu
Study contacts (from the official record)
- Heidi Jacobe, MD, MSCS · 214.633.1837 · heidi.jacobe@utsouthwestern.edu
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