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Probiotic Saccharomyces Boulardii for the Prevention of Antibiotic-associated Diarrhoea (SacBo)

Primary Purpose

Antibiotic-associated Diarrhea, Clostridium Difficile, Diarrhea

Status
Terminated
Phase
Phase 3
Locations
Germany
Study Type
Interventional
Intervention
Saccharomyces boulardii
Placebo
Sponsored by
Bernhard Nocht Institute for Tropical Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Antibiotic-associated Diarrhea focused on measuring antibiotic, associated, diarrhoea, saccharomyces boulardii, Antibiotic-associated diarrhoea (AAD), Clostridium difficile-associated-diarrhoea (CDAD)

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • adult patient (≥ 18 years)
  • patient hospitalized
  • patient receives systemic antibiotic treatment
  • patient contractually capable
  • patient able to follow study procedures
  • informed consent of patient

Exclusion Criteria:

  • allergy against yeast and/or Perenterol® forte und/oder placebos containing Saccharomyces cerevisiae HANSEN CBS 5926, lactose-monohydrate, magnesium stearate, gelatine, sodium dodecyl sulfate, titan dioxide, microcrystalline cellulose.
  • central venous catheter
  • immunosuppression
  • diarrhoea and/or chronic diarrhoea
  • regular intake of Perenterol®, Perenterol® forte oder Yomogi® in the last seven days before the start of the study
  • systemic antimycotic treatment
  • systemic antibiotic treatment within the last 6 weeks
  • no protection against conception, pregnancy, or lactation
  • simultaneous participation in other clinical trials

Sites / Locations

  • Abteilung Innere Medizin, Bundeswehrkrankenhaus Ulm
  • Klinik und Poliklinik für Innere Medizin, Abteilung für Tropenmedizin und Infektionskrankheiten, Universitätsklinikum Rostock
  • Diakoniekrankenhaus Rotenburg (Wümme) gGmbH, Zentrum für Pneumologie
  • Knappschaftskrankenhaus Bottrop, Medizinische Klinik
  • Abteilung Akut-Geriatrie, Ev. Krankenhaus Bethanien Iserlohn
  • Klinikum Vest GmbH, Behandlungszentrum Paracelsus-Klinik Marl
  • I. Medizinische Klinik und Poliklinik, Johannes-Gutenberg-Universität Mainz
  • Klinikum Saarbrücken
  • Klinikum St.Georg, Klinik für Infektiologie, Tropenmedizin und Nephrologie
  • Abt. Innere Medizin, Krankenhaus Reinbek, St. Adolf -Stift
  • Klinikum Bremen Ost, Klinik für Innere Medizin
  • I. Medizinische Klinik und Poliklinik, Universitätsklinikum Hamburg-Eppendorf
  • Agaplesion Diakonieklinikum Hamburg, Klinik für Innere Medizin
  • Bethesda Krankenhaus Bergedorf, Klinik für Innere Medizin

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Saccharomyces boulardii

Microcristallin cellulose

Arm Description

Participants received Saccharomyces boulardii 250 mg capsules twice per day within 24 hours of initiating antibiotic treatment and continued treatment for 7 days after antibiotic discontinuation

Participants received matching placebo twice per day within 24 hours of initiating antibiotic treatment and continued treatment for 7 days after antibiotic discontinuation

Outcomes

Primary Outcome Measures

Total Number of Antibiotic-associated Diarrhea Episodes

Secondary Outcome Measures

Total Number of Clostridium Difficile-associated Diarrhea Episodes
Total Number of Antibiotic-associated Diarrhea Episodes Without Evidence of Clostridium Difficile (Toxins)
Incidence Density of Antibiotic-associated Diarrhea
Average Duration of Antibiotic-associated Diarrhoea and Clostridium Difficile-associated Diarrhea
Average Number of Bowel Movements in Patients With Antibiotic-associated Diarrhoea and Clostridium Difficile-associated Diarrhea
Total Number of Discontinuation or Change of Initially Prescribed Antibiotic

Full Information

First Posted
June 11, 2010
Last Updated
June 7, 2016
Sponsor
Bernhard Nocht Institute for Tropical Medicine
Collaborators
German Federal Ministry of Education and Research
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1. Study Identification

Unique Protocol Identification Number
NCT01143272
Brief Title
Probiotic Saccharomyces Boulardii for the Prevention of Antibiotic-associated Diarrhoea
Acronym
SacBo
Official Title
Saccharomyces Boulardii for the Prevention of Antibiotic-associated Diarrhoea - Randomised, Double-blind, Placebo-controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2016
Overall Recruitment Status
Terminated
Why Stopped
Masked independent interim analysis: completion of the trial was unlikely.
Study Start Date
June 2010 (undefined)
Primary Completion Date
October 2012 (Actual)
Study Completion Date
October 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Bernhard Nocht Institute for Tropical Medicine
Collaborators
German Federal Ministry of Education and Research

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
When patients in hospitals receive antibiotics they often develop diarrhoea. The consequences may be grave for the patient. Thus far, no preventive measure is available. The investigators hypothesize that the apathogenic yeast Saccharomyces boulardii, administered in addition to the antibiotic, may prevent episodes of diarrhoea or may lead to less pronounced diarrhoea. To test this hypothesis, the investigators are carrying out a clinical trial in 1520 adult patients in several hospitals.
Detailed Description
Antibiotic-associated diarrhoea (AAD) is a frequent condition in hospitalised patients receiving antibiotic treatment. The same is true for Clostridium difficile-associated diarrhoea (CDAD) with even more grave consequences of increased morbidity and mortality. The development and evaluation of preventive strategies is one key public health challenge. In the absence of clinically evaluated alternatives, probiotics have been suggested to be beneficial for the prevention of AAD and CDAD. However, data have so far been inconclusive and recently published meta-analyses strongly recommended large state-of-the-art clinical trials on probiotic substances for the prevention of AAD and CDAD. Since the efficacy, side-effects and modes of action of different probiotic bacteria and yeast are strain specific, benefits and risks cannot be generalised. The non-pathogenic yeast Saccharomyces cerevisiae var. boulardii (Sac. boulardii) is considered the most promising probiotic substance for the prevention of AAD and CDAD. We carry out a randomised, placebo controlled, double blind multicentre clinical trial to evaluate Sac. boulardii for the indication of prevention of AAD and CDAD in 1520 adult, hospitalised patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Antibiotic-associated Diarrhea, Clostridium Difficile, Diarrhea
Keywords
antibiotic, associated, diarrhoea, saccharomyces boulardii, Antibiotic-associated diarrhoea (AAD), Clostridium difficile-associated-diarrhoea (CDAD)

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
477 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Saccharomyces boulardii
Arm Type
Active Comparator
Arm Description
Participants received Saccharomyces boulardii 250 mg capsules twice per day within 24 hours of initiating antibiotic treatment and continued treatment for 7 days after antibiotic discontinuation
Arm Title
Microcristallin cellulose
Arm Type
Placebo Comparator
Arm Description
Participants received matching placebo twice per day within 24 hours of initiating antibiotic treatment and continued treatment for 7 days after antibiotic discontinuation
Intervention Type
Drug
Intervention Name(s)
Saccharomyces boulardii
Other Intervention Name(s)
Perenterol® Forte
Intervention Description
Units: 500 mg per day Route of administration : Oral Use Hard-Capsule
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Microcristallin cellulose, Matching capsules containing no active ingredients
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
Total Number of Antibiotic-associated Diarrhea Episodes
Time Frame
29 months
Secondary Outcome Measure Information:
Title
Total Number of Clostridium Difficile-associated Diarrhea Episodes
Time Frame
29 months
Title
Total Number of Antibiotic-associated Diarrhea Episodes Without Evidence of Clostridium Difficile (Toxins)
Time Frame
29 months
Title
Incidence Density of Antibiotic-associated Diarrhea
Time Frame
29 months
Title
Average Duration of Antibiotic-associated Diarrhoea and Clostridium Difficile-associated Diarrhea
Time Frame
29 months
Title
Average Number of Bowel Movements in Patients With Antibiotic-associated Diarrhoea and Clostridium Difficile-associated Diarrhea
Time Frame
29 months
Title
Total Number of Discontinuation or Change of Initially Prescribed Antibiotic
Time Frame
29 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: adult patient (≥ 18 years) patient hospitalized patient receives systemic antibiotic treatment patient contractually capable patient able to follow study procedures informed consent of patient Exclusion Criteria: allergy against yeast and/or Perenterol® forte und/oder placebos containing Saccharomyces cerevisiae HANSEN CBS 5926, lactose-monohydrate, magnesium stearate, gelatine, sodium dodecyl sulfate, titan dioxide, microcrystalline cellulose. central venous catheter immunosuppression diarrhoea and/or chronic diarrhoea regular intake of Perenterol®, Perenterol® forte oder Yomogi® in the last seven days before the start of the study systemic antimycotic treatment systemic antibiotic treatment within the last 6 weeks no protection against conception, pregnancy, or lactation simultaneous participation in other clinical trials
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Stephan Ehrhardt, MD, MPH
Organizational Affiliation
Bernhard Nocht Institute for Tropical Medicine, Hamburg, Germany
Official's Role
Principal Investigator
Facility Information:
Facility Name
Abteilung Innere Medizin, Bundeswehrkrankenhaus Ulm
City
Ulm
State/Province
Baden-Würtemberg
ZIP/Postal Code
89081
Country
Germany
Facility Name
Klinik und Poliklinik für Innere Medizin, Abteilung für Tropenmedizin und Infektionskrankheiten, Universitätsklinikum Rostock
City
Rostock
State/Province
Mecklenburg-Vorpommern
ZIP/Postal Code
18057
Country
Germany
Facility Name
Diakoniekrankenhaus Rotenburg (Wümme) gGmbH, Zentrum für Pneumologie
City
Rotenburg
State/Province
Niedersachsen
ZIP/Postal Code
27356
Country
Germany
Facility Name
Knappschaftskrankenhaus Bottrop, Medizinische Klinik
City
Bottrop
State/Province
Nordrhein-Westfalen
ZIP/Postal Code
46242
Country
Germany
Facility Name
Abteilung Akut-Geriatrie, Ev. Krankenhaus Bethanien Iserlohn
City
Iserlohn
State/Province
Nordrhein-Westfalen
ZIP/Postal Code
58644
Country
Germany
Facility Name
Klinikum Vest GmbH, Behandlungszentrum Paracelsus-Klinik Marl
City
Marl
State/Province
Nordrhein-Westfalen
ZIP/Postal Code
45770
Country
Germany
Facility Name
I. Medizinische Klinik und Poliklinik, Johannes-Gutenberg-Universität Mainz
City
Mainz
State/Province
Rheinland-Pfalz
ZIP/Postal Code
55131
Country
Germany
Facility Name
Klinikum Saarbrücken
City
Saarbrücken
State/Province
Saarland
ZIP/Postal Code
66119
Country
Germany
Facility Name
Klinikum St.Georg, Klinik für Infektiologie, Tropenmedizin und Nephrologie
City
Leipzig
State/Province
Sachsen
ZIP/Postal Code
04129
Country
Germany
Facility Name
Abt. Innere Medizin, Krankenhaus Reinbek, St. Adolf -Stift
City
Reinbek
State/Province
Schleswig-Holstein
ZIP/Postal Code
21465
Country
Germany
Facility Name
Klinikum Bremen Ost, Klinik für Innere Medizin
City
Bremen
ZIP/Postal Code
28325
Country
Germany
Facility Name
I. Medizinische Klinik und Poliklinik, Universitätsklinikum Hamburg-Eppendorf
City
Hamburg
ZIP/Postal Code
20246
Country
Germany
Facility Name
Agaplesion Diakonieklinikum Hamburg, Klinik für Innere Medizin
City
Hamburg
ZIP/Postal Code
20259
Country
Germany
Facility Name
Bethesda Krankenhaus Bergedorf, Klinik für Innere Medizin
City
Hamburg
ZIP/Postal Code
21029
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
26973849
Citation
Ehrhardt S, Guo N, Hinz R, Schoppen S, May J, Reiser M, Schroeder MP, Schmiedel S, Keuchel M, Reisinger EC, Langeheinecke A, de Weerth A, Schuchmann M, Schaberg T, Ligges S, Eveslage M, Hagen RM, Burchard GD, Lohse AW. Saccharomyces boulardii to Prevent Antibiotic-Associated Diarrhea: A Randomized, Double-Masked, Placebo-Controlled Trial. Open Forum Infect Dis. 2016 Jan 29;3(1):ofw011. doi: 10.1093/ofid/ofw011. eCollection 2016 Jan.
Results Reference
derived
Links:
URL
http://www.bni-hamburg.de
Description
Sponsor website

Learn more about this trial

Probiotic Saccharomyces Boulardii for the Prevention of Antibiotic-associated Diarrhoea

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