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Role Of Lactobacillus Reuteri DSM 17938 In The Non-Complicated Diverticular Disease (ReDiCo)

Primary Purpose

Diverticulosis, Diverticulitis

Status
Unknown status
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Lactobacillus Reuterii
placebo
Sponsored by
Casa Sollievo della Sofferenza IRCCS
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diverticulosis focused on measuring Diverticula, Diverticular disease, Diverticulitis, Probiotics

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adult patients affected by symptomatic diverticulosis
  • Informed consent obtained and signed.
  • Expected compliance

Exclusion Criteria:

  • Patients supplemented with other probiotics
  • Patients treated with antibiotics
  • Patients affected by hearth failure, renal failure, neoplasia

Sites / Locations

  • Careggi Hospital
  • Casa Sollievo della Sofferenza Hospital - IRCCSRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Lactobacillus Reuterii

Placebo

Arm Description

Outcomes

Primary Outcome Measures

Reduction of 50% of the score of activity of the diverticular disease
A validated questionnaire was used to investigate on intestinal symptoms. The following symptoms/signs will be investigated: Abdominal pain Abdominal bloating Urgency Diarrhoea Abdominal Tension Each factor previously listed will be graded according to the following scale of gravity: 0= no symptom 1= light disturbance 2= moderate disturbance 3= serious disturbance The score of activities can range between 0 (asymptomatic patient) to 15 (serious disturbances with important impacts on the quality of life).

Secondary Outcome Measures

Reduction of 20% of acute diverticulitis episodes
To value the efficancy in reduction of acute diverticulitis, defined as episodes of abdominal pain associated with fever and/or abdominal resistance, increment of ESR and neutrophil leucocitosis and that demand a treatment of systemic antibiotics

Full Information

First Posted
July 22, 2010
Last Updated
June 27, 2011
Sponsor
Casa Sollievo della Sofferenza IRCCS
Collaborators
Careggi Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01168154
Brief Title
Role Of Lactobacillus Reuteri DSM 17938 In The Non-Complicated Diverticular Disease
Acronym
ReDiCo
Official Title
Phase 3 Study of Lactobacillus Reuterii in Patients With Symptomatic Non-complicated Diverticular Disease
Study Type
Interventional

2. Study Status

Record Verification Date
October 2008
Overall Recruitment Status
Unknown status
Study Start Date
February 2009 (undefined)
Primary Completion Date
December 2012 (Anticipated)
Study Completion Date
December 2013 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
Casa Sollievo della Sofferenza IRCCS
Collaborators
Careggi Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this study is to evaluate the effectiveness and the tolerability of the Lactobacillus reuteri in the control of the diverticular disease symptoms and in the prevention of acute diverticulitis episodes.
Detailed Description
The gastrointestinal apparatus hosts a bacterial population that quantifies to around 1011 microorganisms per gram of content with more than 400 different species. Its principal functions are: metabolic, trophic, and protective. The Lactobacillus reuteri (Reuterin®) is considered one of the few native species in the human intestinal tract. It is able to modulate the immune response CD4+ T-Helper to an ileum level. Lactobacillus reuteri isolated for the first time in 1980 is a heterofermantative species. Its probiotic activity is attributed to the ability to exercise an inhibitive effect on the pathogenic micro-organisms with a combination of mechanisms including the production of lactic acid, hydrogen peroxide, antimicrobic substances and bactericide. Moreover, Lactobacillus reuteri is in a position to produce various short chain-like fat acids such as the acetic acid from the fermentation of carbohydrates. At last, it is in a position to produce a powerful antimicrob substance known as Reuterina that is capable of inhibiting the growth of many bacterial species including Escherichia, Salmonella, Shigella, Proteus, Pseudomonas, Clostridium and Sfafilococcus as well as fungi and protozoa, many of which are pathogens for man. Among pathologies in which it is hypothesized that probiotics could have a possible therapeutic role, there is the diverticulosis disease. Approximately 20% of patients with colonic diverticula have intestinal disturbances and a reduction of the quality of life. Moreover approximately 20% of the patients with diverticulosis in the colon have at least 1 acute diverticulitis attack, characterized by pain, fever, abdominal defence, increment of the VES and neutrophil leucocytosis. Usually the acute diverticulitis episode can be controlled by medical therapy, but repeated episodes in time often lead to greater complications in the perforation, from the abdominal abscesses, from the fistulas and from the stenosis. The prevention of acute diverticulitis episodes is therefore very important so as to prevent greater complications of such pathology. Until now, the scientific evidences have suggested the use of fibre and non-absorbable antibiotics (such as rifaximine) for the treatment of a non-complicated diverticular disease and for the prophylaxis of the feared complications. The extended use of antibiotics exposes to the risk of selecting resistant strains and there are no long-term studies on the outcome of the patients suffering from diverticulosis in continuous therapy with rifaximine and fibres. The therapy with Lactobacillus reuteri could be effective in the control of symptoms of the diverticular disease through its trophic action on coloncytes (thanks to the SCFA production), both through the modulation of the activity of the immune system and on the intestinal permeability. Moreover the antibacterial activity of Lactobacillus reuteri against the pathogenic bacteria could be useful in the prevention and the treatment of acute diverticulitis episodes. Finally, thanks to its trophic role on the intestinal epithelium, Lactobacillus reuteri could help the mucosal cure of acute diverticulitis episodes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diverticulosis, Diverticulitis
Keywords
Diverticula, Diverticular disease, Diverticulitis, Probiotics

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
160 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Lactobacillus Reuterii
Arm Type
Active Comparator
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Dietary Supplement
Intervention Name(s)
Lactobacillus Reuterii
Intervention Description
Lactobacillus Reuterii 10000000000 CFU per day
Intervention Type
Dietary Supplement
Intervention Name(s)
placebo
Intervention Description
placebo
Primary Outcome Measure Information:
Title
Reduction of 50% of the score of activity of the diverticular disease
Description
A validated questionnaire was used to investigate on intestinal symptoms. The following symptoms/signs will be investigated: Abdominal pain Abdominal bloating Urgency Diarrhoea Abdominal Tension Each factor previously listed will be graded according to the following scale of gravity: 0= no symptom 1= light disturbance 2= moderate disturbance 3= serious disturbance The score of activities can range between 0 (asymptomatic patient) to 15 (serious disturbances with important impacts on the quality of life).
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Reduction of 20% of acute diverticulitis episodes
Description
To value the efficancy in reduction of acute diverticulitis, defined as episodes of abdominal pain associated with fever and/or abdominal resistance, increment of ESR and neutrophil leucocitosis and that demand a treatment of systemic antibiotics
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients affected by symptomatic diverticulosis Informed consent obtained and signed. Expected compliance Exclusion Criteria: Patients supplemented with other probiotics Patients treated with antibiotics Patients affected by hearth failure, renal failure, neoplasia
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Fabrizio Bossa, MD
Phone
00390882410235
Email
f.bossa@operapadrepio.it
First Name & Middle Initial & Last Name or Official Title & Degree
Angelo Andriulli, MD
Phone
00390882410263
Email
a.andriulli@operapadrepio.it
Facility Information:
Facility Name
Careggi Hospital
City
Florence
ZIP/Postal Code
50141
Country
Italy
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vito Annese, MD
Phone
00390557946035
Email
annesev@aou-careggi.toscana.it
First Name & Middle Initial & Last Name & Degree
Vito Annese, MD
Facility Name
Casa Sollievo della Sofferenza Hospital - IRCCS
City
San Giovanni Rotondo
ZIP/Postal Code
71013
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Fabrizio Bossa, MD
Phone
00390882410235
Email
f.bossa@operapadrepio.it
First Name & Middle Initial & Last Name & Degree
Angelo Andriulli, MD
Phone
00390882410263
Email
a.andriulli@operapadrepio.it
First Name & Middle Initial & Last Name & Degree
Fabrizio Bossa, MD

12. IPD Sharing Statement

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Role Of Lactobacillus Reuteri DSM 17938 In The Non-Complicated Diverticular Disease

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