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Updated on 28 April 2025

Summary

The research study is being done to understand both why and how scleroderma and related female-biased diseases affect women and men differently.  Though we do not know what causes these diseases, we do know that women are much more likely to develop them than men.  We are studying how the body’s immune system differs between men and women with these conditions, and comparing this to people who do not have these diseases. 

We are looking for men and women without scleroderma and related diseases (control group) to have one study visit that includes a physical exam and blood collection.  We will also collect information about you from your medical record for up to 5 years.  Participants will receive a stipend of $50 for participating.  

You must not have scleroderma, pulmonary hypertension, diseases with similarities to scleroderma (including myositis, lupus, Sjogren’s syndrome, or rheumatoid arthritis), or other conditions that affect your immune system.

Description

 

Participants will be asked to provide biological samples at different time points during your pregnancy and delivery of your baby.  
 

These samples may be collected when you are getting other clinical tests done or you may be asked to have your blood drawn utilizing a drive up location or research visit.  
 

Your health information will also be collected.

Details
Condition Medical Research
Age 99years or below
Clinical Study Identifier15
Last Modified on28 April 2025

Eligibility

Dear Participant,

Thank you for your interest in the 

[Trial Name] study. 

We appreciate you taking the time to learn more about this important research.

  • We are writing to inform you that at this time, enrollment for [Trial Name] is being conducted
  • This means that we are currently reaching out directly to individuals who have been specifically identified as potentially eligible based on pre-screening or other criteria. We are not actively recruiting new participants through general outreach at this moment.

 

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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