Clostridium Difficile
Conditions
Brief summary
A total of 440 patients meeting enrollment criteria with a primary episode of C. Difficile Infection (CDI) will be enrolled across 3 sites. The total study time period for study procedures followed by clinical monitoring is anticipated to be about 24 months (biomarker assays and other analyses may be completed after the 24 month time period). All participants will receive oral antibiotics for CDI under the care of their physician. After consenting to participate in the study, participants will be randomized to receive either misoprostol (200 mcg po BID) or matching placebo for 14 days. Participants will be monitored for a total time-period of approximately 9 weeks with the goal of monitoring for recurrence of CDI during an 8-week follow-up period from the time that the course of antibiotic treatment is completed. Patients will have blood and stool samples (or rectal swabs if participants are unable to provide a stool sample) collected throughout the study to assess adherence, biomarkers, and to confirm recurrence of CDI (if necessary).
Interventions
Two 100mcg capsules twice per day
OTHERPlacebo
Two capsules twice per day
Sponsors
National Institutes of Health (NIH)
Vanderbilt University Medical Center
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1. Episode of CDI, defined as ALL of the following: 1. ≥3 unformed (loose or watery) stools with a 24-hour period; 2. A documented positive C. difficile toxin assay (enzyme immunoassay \[EIA\] or cell cytotoxicity assay) or NAAT for toxigenic C. difficile from a stool sample collected while the subject was symptomatic; and 3. No other explanation for diarrhea (e.g. laxatives). 2. At the time of enrollment, on a course of oral antibiotics commonly used for treatment of CDI. 3. Be ≥18 years of age. 4. Be able to provide signed and dated informed consent. 5. Must be able to read and understand English.
Exclusion criteria
1. Have not recovered from primary episode of CDI at time of enrollment, defined as presence of EITHER of the following: 1. ≥3 unformed (loose or watery) stools during the 24 hours prior to randomization, OR 2. Abdominal discomfort (more than mild) present during the 24 hours prior to randomization. 2. Have received, or plans to use, any of the following for treatment of the primary episode of CDI: 1. Any immunotherapy (e.g., intravenous immunoglobulin, bezlotoxumab). 2. Any toxin-binding therapy (e.g., cholestyramine \[Questran\], colestipol \[Colestid\], or colesevelam \[Welchol\]). 3. Current or planned treatment with prostanoid therapy. 4. Diarrhea caused by another infection or diarrhea caused by an underlying gastrointestinal disorder. 5. Have any contraindication to oral/enteral therapy (e.g., severe nausa/vomiting or ileus). 6. Have an absolute neutrophil count \<500/mm3 \[1.0 x 109/L\] within 30 days of screening. 7. Require or have an anticipated need for mechanical ventilation or vasopressors for hemodynamic support during the study. 8. Pregnant, nursing, or planning to become pregnant. 9. Inability to understand the requirements of the study, inability to abide by the study restrictions. 10. Have any clinically significant medical or surgical condition that in the investigator's opinion could interfere with the administration of study drug, interpretation of study results, or compromise the safety or well-being of the subject. 11. Known hypersensitivity to misoprostol. 12. Be unwilling or unable to follow study procedures (e.g., study visits, swallow the study drug/placebo, provide stool samples and undergo phlebotomy according to the study schedule, and reliably report information by phone), or not have a caregiver who can ensure that study procedures are followed. 13. If female, be pre-menopausal (cessation of menses less than or equal to 1 year) and not surgically/medically sterile or not following acceptable non-hormonal method of birth control such as abstinence, intrauterine device, or barrier control for at least 1 complete menstrual cycle before the screening visit, or not using estrogen/progestin containing products for at least 2 months before the screening visit through discharge from the study. 14. Unreliable access to telephone service to allow for contact with study personnel. 15. Inability to be seen for routine clinical care either as an outpatient or inpatient.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Number of Participants With Clinical Recurrence of Clostridium Difficile Infection (CDI). | 8 weeks | Number of Participants with clinical recurrence of Clostridium Difficile Infection (CDI) in the 8 week follow-up period. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Number of Recurrences During the Follow-up Period | 8 weeks | Number of recurrences during the follow-up period (for those who have a first recurrence during the follow-up time period) |
| Time to Resolution of Diarrhea | 8 weeks | Time to resolution of diarrhea (TTROD; for those with recurrence) |
Countries
United States
Participant flow
Recruitment details
Due to low enrollment the study was closed early.
Participants by arm
| Arm | Count |
|---|---|
| Study Drug (Misoprostol) Misoprostol 100Mcg Tab: Two 100mcg capsules twice per day | 3 |
| Placebo Placebo: Two capsules twice per day | 3 |
| Total | 6 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Overall Study | Lost to Follow-up | 1 | 0 |
Baseline characteristics
| Characteristic | Study Drug (Misoprostol) | Placebo | Total |
|---|---|---|---|
| Age, Categorical <=18 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical >=65 years | 1 Participants | 0 Participants | 1 Participants |
| Age, Categorical Between 18 and 65 years | 2 Participants | 3 Participants | 5 Participants |
| Ethnicity (NIH/OMB) Hispanic or Latino | 0 Participants | 0 Participants | 0 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 3 Participants | 3 Participants | 6 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) White | 3 Participants | 3 Participants | 6 Participants |
| Region of Enrollment United States | 3 participants | 3 participants | 6 participants |
| Sex: Female, Male Female | 2 Participants | 3 Participants | 5 Participants |
| Sex: Female, Male Male | 1 Participants | 0 Participants | 1 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 3 | 0 / 3 |
| other Total, other adverse events | 0 / 3 | 0 / 3 |
| serious Total, serious adverse events | 0 / 3 | 0 / 3 |
Outcome results
Primary
Number of Participants With Clinical Recurrence of Clostridium Difficile Infection (CDI).
Number of Participants with clinical recurrence of Clostridium Difficile Infection (CDI) in the 8 week follow-up period.
Time frame: 8 weeks
| Arm | Measure | Value (COUNT_OF_PARTICIPANTS) |
|---|---|---|
| Study Drug (Misoprostol) | Number of Participants With Clinical Recurrence of Clostridium Difficile Infection (CDI). | 0 Participants |
| Placebo | Number of Participants With Clinical Recurrence of Clostridium Difficile Infection (CDI). | 0 Participants |
Secondary
Number of Recurrences During the Follow-up Period
Number of recurrences during the follow-up period (for those who have a first recurrence during the follow-up time period)
Time frame: 8 weeks
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Study Drug (Misoprostol) | Number of Recurrences During the Follow-up Period | 0 number of events |
| Placebo | Number of Recurrences During the Follow-up Period | 0 number of events |
Secondary
Time to Resolution of Diarrhea
Time to resolution of diarrhea (TTROD; for those with recurrence)
Time frame: 8 weeks
Population: These data were not collected because no participants experienced recurrence.