Lactobacillus Reuteri in the Prevention of Antibiotic Associated-diarrhea and Clostridium Difficile

Case Western Reserve University

Status: Completed

Conditions: Antibiotic-associated Diarrhea; Clostridium Difficile

Treatments: Dietary Supplement: Lactobacillus reuteri

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT02127814

RES504803

Details and patient eligibility

About

The purpose of this study is to find whether Lactobacillus reuteri prevents antibiotic-associated diarrhea and related Clostridium difficile infections. Subjects will be admitted from the University Hospitals Case Medical Center. They will be randomly assigned to an intervention group receiving L. reuteri or a placebo. Supplementation will occur during antibiotic treatment and for an additional 7 days after cessation of treatment. Data collection will occur at baseline, end of antibiotic use, 7 days after antibiotic cessation, and 21 days after antibiotic cessation. Primary data includes diarrhea instances. Secondary data includes severity of diarrhea, presence of C. difficile toxins, and presence of other GI symptoms.

Full description

The data being measured for this study include:

Primary outcome = incidence of diarrhea during and after treatment with antibiotics. An episode of diarrhea is defined as the discrete period between the time when stool output meets or exceeds three soft and unformed or watery bowel movements to the time when formed stools return, which must be at least 48 hours later.

Secondary variables:

1. severity of diarrhea measured as the discrete period between the time when stool output meets or exceeds 3 soft and unformed or watery bowel movements to the time when formed stools return.
2. frequency of stool samples positive for C. Difficile toxin A or B at baseline, when presenting with diarrhea during the study period, and at the follow-up 21 days post-antibiotic-treatment to detect possible clearance of C. Difficile, in patients ingesting L. reuteri versus placebo.
3. frequencies of other gastrointestinal symptoms at 1, 2, and 4 weeks, in the L. reuteri group versus placebo and assessed by the validated Gastrointestinal Symptom Rating Score.

Enrollment: 73 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Receiving antibiotics for not more than 48 hours prior to enrollment and free from diarrhea
• able to understand and sign informed consent and HIPPA
• available throughout the study period
• subjects should have the mental ability to understand and willingness to fulfill all the details of the protocol

Exclusion criteria

• three or more soft and unformed or watery stools per day at admission
• receiving chemotherapy or radiation therapy
• diagnosis of inflammatory bowel disease
• NPO without PO meds
• neutropenia (an absolute neutrophil count (ANC) of less than 1500/microL)
• HIV positive with a CD4+ T-lymphocyte count <400 per mcL blood
• requiring care in an intensive care unit
• status-post bowel resection during hospitalization
• patient's receiving antibiotics four weeks prior to hospitalization
• patient with severe life threatening illness or immunocompromised
• pregnancy

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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73 participants in 2 patient groups, including a placebo group

L. reuteri

Experimental group

Treatment:

Dietary Supplement: Lactobacillus reuteri

Identical Placebo

Placebo Comparator group

Treatment:

Dietary Supplement: Lactobacillus reuteri