Blood Sample for Crohns Disease or Ulcerative Colitis (UC)

  • STATUS
    Recruiting
Updated on 23 November 2020

Summary

The PRECIOUS Study: Predicting Crohn’s & Colitis Outcomes in the United States If you are between the ages of 16-80 and suffer from Crohn’s disease or ulcerative colitis (UC), you may be eligible to participate in this research study.

What is this study about?

The PRECIOUS study is testing the ability of a blood test called PredictSURE IBD™ to determine whether your disease will follow a mild or aggressive course. The test has already been demonstrated to work well in a UK population, so the PRECIOUS study aims to confirm this result in a different group of patients.

 

Description

What are the benefits?

  • If the study is successful, it will provide further evidence for the use of the test to drive treatment decisions in IBD and will be the first step towards personalized medicine in the US.
  • We will reimburse any reasonable travel and parking costs up to a value of $50.

Details
Condition Cushing's disease
Clinical Study IdentifierTX231620
Last Modified on23 November 2020

Eligibility

Yes No Not Sure

Inclusion Criteria

Is your age between 16 yrs and 80 yrs?
Gender: Male or Female
Do you have Cushing's disease?
Who can participate?
The target patient population is newly diagnosed, treatment naive patients with active Crohn’s disease or UC Not currently on steroids, and at least 7 days since last steroid use Experiencing a flare or period of active disease Not scheduled to start biologics as first line therapy
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How to participate?

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What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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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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