A Non-Interventional Pilot Study to Explore the Role of Gut Flora in Clostridoides Difficile Infection

Withdrawn before enrolling

Conditions studied: Clostridium Difficile, Clostridium Difficile Infection, Microbiome, CDI

In brief

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

Key facts

Study ID

NCT04100603

Run by

ProgenaBiome

People needed

0

Starts

2020-03-02

Expected to finish

2030-07-31

Last updated by the study team

2025-06-05

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Willingness to sign informed consent
• Diagnosis of C. difficile infection
• Age of 18 and older

You may not qualify if…

• Refusal by patient to sign informed consent form
• Treatment with antibiotics 2 weeks prior to screening
• Treatment with probiotics 6 weeks prior to screening
• 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
• Any clinically significant evidence of disease that could interfere with the subject's ability to enter the trial
• Inability of patient to adequately communicate with the investigator or their respective designee and/or comply with the requirements of the entire study

Where it is running

• ProgenaBiome — Ventura, California, United States

Full record on ClinicalTrials.gov

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