A Pilot Study to Explore the Role of Gut Flora in Gout

  • STATUS
    Recruiting
  • End date
    Jul 9, 2023
  • participants needed
    100
  • sponsor
    ProgenaBiome
Updated on 12 September 2021

Summary

This study seeks to correlate microbiome sequencing data with information provided by patients and their medical records.

Description

The goal of this Research Study is to better understand how the genetic information in subject's microbiome correlates to Gout

Details
Condition Arthritis, Gout, Arthritis and Arthritic Pain, Gout (Hyperuricemia), Arthritis and Arthritic Pain (Pediatric)
Treatment No intervention
Clinical Study IdentifierNCT04224662
SponsorProgenaBiome
Last Modified on12 September 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Signed informed consent, demonstrating that the patient understands the procedures required for the study and the purpose of the study i. May be signed by parent or legal guardian in the case of minor or adult unable to provide consent
Male or female of all ages. (interest is given to children who present with autism or Crohn's and whose parents wish to analyze their children's gut flora. Also of interest analysis of development of the child's microbiome. In the case of autism, the younger the child, the better to correct the neurological problems if an association is found between autism and the microbiome)
Diagnosis of Gout by a physician

Exclusion Criteria

Refusal to sign informed consent form
History of bariatric surgery, total colectomy with ileorectal anastomosis or proctocolectomy
Postoperative stoma, ostomy, or ileoanal pouch
Participation in any experimental drug protocol within the past 12 weeks
Treatment with total parenteral nutrition
Clear my responses

How to participate?

Step 1 Connect with a study center
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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