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

Inclusion Criteria: * Willingness to sign informed consent * Diagnosis of C. difficile infection * Age of 18 and older Exclusion Criteria: * 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