Microbial Restoration for Individuals With One or More Recurrences of Clostridium Difficile Associated Disease (CDAD)
Multi-center, randomized, placebo controlled, partially blinded trial comparing the safety and efficacy of fecal microbiota transplantation versus placebo both delivered by rectal enema in subjects 18 years of age or older with recurrent Clostridium difficile Associated Disease (CDAD). 162 male or female subjects will be enrolled in the study. Enrolled subjects will be randomized at each site to receive either FMT by enema or placebo by enema in a 2:1 ratio. Study duration is 4 years, subject participation duration is approximately 3 years. Primary study objectives are to: 1) evaluate the safety of FMT(s) delivered by enema vs. placebo delivered by enema, 2) determine efficacy of FMT delivered by enema vs. placebo delivered by enema
- Clostridial Infection
- Probiotic Therapy
- Eligible Ages
- Between 18 Years and 99 Years
- Eligible Genders
- Accepts Healthy Volunteers
- Providing permission to access the medical record.
- Male or non-pregnant female 18 years or older at the time of enrollment.
- Able to provide signed and dated informed consent.
- = / > 2 episodes of CDAD in the past 6 months, including the last episode if present at screening*.
*Defined by = / > 1 confirmed positive CDAD by diagnostic methods and another occurrence substantiated by medical history.
5. Completed treatment course of at least 10 days of oral vancomycin, oral/IV metronidazole, or oral fidaxomicin for the most recent episode prior to enrollment.
6. Controlled diarrheal symptoms (<3 unformed stools per 24 consecutive hour period).
7. Deemed likely to survive for 1 year after enrollment.
8. Women of childbearing potential** (includes females who are postmenopausal <1 year) in sexual relationships with men must use an acceptable method of contraception*** from 30 days prior to enrollment until 4 weeks after completing study treatment.
**Not sterilized via tubal ligation, bilateral oophorectomy, salpingectomy, hysterectomy, or successful Essure(R) placement (permanent, non-surgical, non-hormonal sterilization) with documented radiological confirmation test at least 90 days after the procedure, and still menstruating or < 1 year of the last menses if menopausal. Also includes females who are postmenopausal < 1 year.
***Includes, but is not limited to, barrier with additional spermicidal foam or jelly, intrauterine device, hormonal contraception (started at least 30 days prior to study enrollment), intercourse with men who underwent vasectomy.
9. Males must agree to avoid impregnation of women between Day 1 and 28 days following each administration of the study product.
10. Negative urine or serum pregnancy test within 24 hours of enrollment and randomization.
11. Is able to provide blood and fecal specimens.
12. Is able to complete a test of comprehension.
- Previous FMT within the previous 12 months prior to study enrollment.
- Use of the following drugs in last 3 months: such as monoclonal antibodies to B and T cells, anti-TNF agents, glucocorticoids*, antimetabolites*, calcineurin inhibitors***, mycophenolate mofetil.
*For example, > 20 mg of prednisone (or equivalent) given daily or on alternative days for 2 weeks or more.
- azathioprine, 6-mercaptopurine
- ,tacrolimus, cyclosporine
3. Requiring antibiotics in the past 2 weeks prior to receiving the enema for a condition other than CDAD or scheduled to be used in the upcoming 2 weeks.
4. Unable to tolerate enema for any reason.
5. Any GI cancer in the past year or any actively treated malignancy.
6. Patients with a history of severe anaphylactic food allergy.
7. Any history of cirrhosis.
8. Untreated HIV disease.****
****If no HIV screening results are available in the medical record from within the last six months, a HIV screening test will be performed during screening.
9. Other severe immunosuppression or immunodeficiency.
10. Severe OR acute disease at the time of enrollment.*****
*****Temperature >100.4 degrees Fahrenheit (38 degrees Celsius) or heart rate less than 45 bpm or greater than 130 bpm, or systolic blood pressure less than 80 mm Hg or greater than 155 mm Hg, or diastolic blood pressure greater than 100 mm Hg, or at the discretion of the investigator
11. Major surgery of the GI tract in the past 6 months.
12. Having a non tolerance****** to or any component of vancomycin, loperamide or GoLYTELY.
******tolerance is defined as the absence of immunoglobulin E-mediated allergy (e.g., urticaria, angioedema, bronchospasm, or anaphylaxis) and the absence of severe allergy (e.g., Stevens-Johnson syndrome/toxic epidermal necrolysis)
13. Any history of inflammatory bowel disease (IBD) including ulcerative colitis, Crohn's disease, indeterminate colitis or celiac disease.
14. Irritable bowel syndrome (IBS) within the past 12 months or any active uncontrolled gastrointestinal disorders or diseases.
*******GI obstruction, ileus, gastric retention, bowel perforation, toxic colitis or toxic megacolon, persistent infectious gastroenteritis, persistent or chronic diarrhea of unknown etiology, or refractory/severe Clostridium difficile infection (severe CDAD identified as leukocytosis with a white blood cell count greater than 15,000 cells/mL or an increase in the serum creatinine level to 1.5 times the premorbid level), chronic diarrhea of unknown cause for 6 weeks or more.
15. Unable to comply with protocol requirements.
16. Participation in any other clinical drug research trial within 30 days prior to enrollment or for 1 year after enrollment that might interfere with the safety and efficacy assessment.
17. A condition that would jeopardize the safety or rights of the subject, would make it unlikely for the subject to complete the study, or would confound the results of the study.
- Phase 1/Phase 2
- Study Type
- Intervention Model
- Sequential Assignment
- Primary Purpose
- Double (Participant, Investigator)
|100 grams of thawed processed stool diluted into 250 ml of saline and delivered by retention enema given 1-3 hours after loperamide 4 mg po x 1, n=108||
|250 ml of saline delivered by retention enema given 1-3 hours after loperamide 4 mg po x 1; if no improvement followed by FMT (100 grams of thawed processed stool diluted into 250 ml of saline and delivered by retention enema given 1-3 hours after loperamide 4 mg po x 1) x 2, n=54||
- NCT ID
- National Institute of Allergy and Infectious Diseases (NIAID)
Study ContactNadine Rouphael
This is a multi-center, randomized, placebo controlled, partially blinded trial comparing the safety and efficacy of fecal microbiota transplantation versus placebo both delivered by rectal enema in subjects 18 years of age or older with recurrent Clostridium difficile Associated Disease (CDAD). 162 (108 in the FMT group, 54 in the placebo group) male or female subjects will be enrolled in the study. Subjects must have had treatment for most recent CDAD with at least 10 days of either metronidazole po/IV (500 mg tid), oral vancomycin (at least 125 mg qid), or oral fidaxomicin (200 mg bid) and have no diarrheal symptoms (<3 unformed stools per 24 hour period) off antibiotics during the washout period. Enrolled subjects will be randomized at each site to receive either FMT by enema or placebo by enema in a 2:1 ratio. The study is described as partially blinded because by design subjects are to be blinded only to a certain point. Subjects will be followed for clinical response (efficacy) and safety. Study duration is 4 years, subject participation duration is approximately 3 years. Primary study objectives are to: 1) evaluate the safety of FMT(s) delivered by enema vs. placebo delivered by enema, 2) determine efficacy of FMT delivered by enema vs. placebo delivered by enema. Secondary objectives are to: 1) evaluate the sustained clinical response rate of FMTs delivered by enema vs. placebo delivered by enema, 2) evaluate the rate of recurrent CDAD, 3) evaluate the time to recurrent CDAD.