Use of Probiotics as Adjunctive Treatment for Chronic Rhinosinusitis
Primary Purpose
Chronic Rhinosinusitis
Status
Completed
Phase
Phase 4
Locations
Study Type
Interventional
Intervention
probiotic containing L.rhamnosus R0011 strain
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Rhinosinusitis
Eligibility Criteria
Inclusion Criteria:
- Age ≥15 and ≤70 years.
The patient must be bothered by each of the two following symptoms(>50% of days in the last 3 months):
A. More than 12 consecutive weeks of symptomatic nasal obstruction and, B. More than 12 weeks of symptomatic nasal discharge.
- An Otolaryngologist evaluation and diagnosis of chronic inflammatory rhinosinusitis (hyperplastic mucosa, polyps in absence of overt bacterial infection)
- Access to telephone (home or person cell).
Exclusion Criteria:
- Sinus surgery within the last 3 months
- Acute illness within the last 2 weeks requiring antibiotics: including: otitis media, pharyngitis, bronchitis, or laryngitis.
- Immunosuppression (due to medications including oral steroids, or due to autoimmune diseases, HIV infection, cystic fibrosis, immunodeficiency, malignancies, uncontrolled diabetes mellitus, chronic renal failure, etc.)
- Patients with chronic or acute bacterial sinusitis.(Clinical diagnosis-to be decided by MD)
- An allergic reaction to a probiotic dietary supplement in the past (such as symptoms of tightness in the chest, breathing difficulties, skin hives, rash or other clinical symptoms consistent with sensitivity or intolerance)
- Inability to speak or read English.
- Pregnancy and Lactation
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Placebo Comparator
Active Comparator
Arm Label
Placebo pill
Probiotic
Arm Description
Placebo pills on same schedule as active intervention.
L. rhamnosus R0011 strain
Outcomes
Primary Outcome Measures
Mean Reduction in SNOT-20 Scores
Mean reduction (and Standard deviation) in SNOT-20 scores, from baseline to 8 week measurements. SinoNasal Outcome Test measures symptom severity. It is a summary score, ranging from 0 to 100 with 100 indicating worse symptoms. Since 100 represents more severe symptoms, the changes represented here are reductions in SNOT-scores, even though they are not expressed as negative numbers.
Secondary Outcome Measures
Side Effect Summary
Totals of all side effects for placebo group and treatment group over the course of the eight week trial (including patients who dropped from the study after baseline measurement). Individual categories of side-effects are listed in Adverse events section.
Mean Number of Days of Antibiotic Use During the Study Period (0-8 Weeks)
Mean number of days that antibiotics were used in the subgroup (placebo vs Probiotic arm)
Mean Number of Days of Steroid Spray Use for Each Group
Full Information
NCT ID
NCT00396162
First Posted
November 2, 2006
Last Updated
August 11, 2016
Sponsor
University of Michigan
Collaborators
Institut Rosell
1. Study Identification
Unique Protocol Identification Number
NCT00396162
Brief Title
Use of Probiotics as Adjunctive Treatment for Chronic Rhinosinusitis
Official Title
Use of Probiotics as Adjunctive Treatment for Chronic Rhinosinusitis
Study Type
Interventional
2. Study Status
Record Verification Date
August 2016
Overall Recruitment Status
Completed
Study Start Date
November 2006 (undefined)
Primary Completion Date
January 2008 (Actual)
Study Completion Date
February 2008 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Michigan
Collaborators
Institut Rosell
4. Oversight
5. Study Description
Brief Summary
Chronic sinusitis is reported to be one of the most widespread disorders in the United States. It can be caused by a variety of reasons such as allergy, infection and/or defects in T-cells which help regulate immune function. Medication and other costs related to treatment of nasal and sinus infections are estimated to be more than $60 million annually putting a considerable strain on the economy of health care.
Probiotics are live microorganisms that are normally present in the gut of a healthy individual. They are also known as "friendly bacteria" and have been used to help maintain the normal functioning of the immune system. They are safe and are commercially available in the form of yoghurt, sachets, chewable tablets or flavored capsules. Since a number of nasal and sinus disorders are related to allergy and improper functioning of the immune system, we hypothesize that regular use of probiotics may help improve chronic nasal and sinus symptoms by boosting immune responses.
The project we propose is novel because it would be the first study evaluating the usefulness of probiotics for the larger population having chronic sinusitis rather than those having only allergic symptoms. We aim to assess whether regular use of probiotics will help improve symptoms of chronic sinusitis and will have a greater effect than placebo in this regard.
Detailed Description
Probiotics are live microorganisms which when administered in adequate amounts confer a health benefit on the host. They are a part of the normal gastrointestinal flora and have safely been used to boost immune responses in patients with perennial and seasonal allergic rhinitis. Their exact mechanism of benefit is unknown but they primarily help to regulate T-cell function which is important in maintaining immune tolerance.
Chronic rhinosinusitis is widely prevalent and affects nearly 16 million people in the US alone each year. It puts a strain on the health resources of the nation in terms of costs related to medications and surgery. Chronic rhinosinusitis can be caused by a variety of reasons including allergy/hypersensitivity, infection, nasal anatomical variations and T-cell regulatory dysfunction. We hypothesize that regular use of probiotics in patients with chronic rhinosinusitis will result in substantial improvement in their symptoms by boosting their immunity and may also help decrease their medication usage.
Our study will be a double-blinded, randomized, control trial. We hope to recruit 100 patients from the University Otolaryngology and Allergy Clinics. Fifty patients will be randomized to the treatment (active) arm and 50 patients to the placebo arm. Subjects will be followed for 2 months during their period of participation in the study.
The main aim of our study is to determine whether regular use of probiotics in patients with chronic rhinosinusitis helps improve their quality of life. Our main outcome of interest is a change in the mean score of the Sino-Nasal Outcome Test (SNOT-20) form in the treatment group and a greater change in the mean score of the SNOT-20 in the treatment arm as compared to the placebo arm. If probiotics are found to be effective, they may be used as a cost-effective, adjunctive therapy for patients with chronic rhinosinusitis.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Rhinosinusitis
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
77 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Placebo pill
Arm Type
Placebo Comparator
Arm Description
Placebo pills on same schedule as active intervention.
Arm Title
Probiotic
Arm Type
Active Comparator
Arm Description
L. rhamnosus R0011 strain
Intervention Type
Drug
Intervention Name(s)
probiotic containing L.rhamnosus R0011 strain
Other Intervention Name(s)
L rhamnosus R0011
Intervention Description
500 million active cells of L rhamnosus R0011 strain per tablet bid for 4 weeks
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo pill
Primary Outcome Measure Information:
Title
Mean Reduction in SNOT-20 Scores
Description
Mean reduction (and Standard deviation) in SNOT-20 scores, from baseline to 8 week measurements. SinoNasal Outcome Test measures symptom severity. It is a summary score, ranging from 0 to 100 with 100 indicating worse symptoms. Since 100 represents more severe symptoms, the changes represented here are reductions in SNOT-scores, even though they are not expressed as negative numbers.
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Side Effect Summary
Description
Totals of all side effects for placebo group and treatment group over the course of the eight week trial (including patients who dropped from the study after baseline measurement). Individual categories of side-effects are listed in Adverse events section.
Time Frame
8 weeks
Title
Mean Number of Days of Antibiotic Use During the Study Period (0-8 Weeks)
Description
Mean number of days that antibiotics were used in the subgroup (placebo vs Probiotic arm)
Time Frame
At 8 weeks after baseline measures
Title
Mean Number of Days of Steroid Spray Use for Each Group
Time Frame
8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
15 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age ≥15 and ≤70 years.
The patient must be bothered by each of the two following symptoms(>50% of days in the last 3 months):
A. More than 12 consecutive weeks of symptomatic nasal obstruction and, B. More than 12 weeks of symptomatic nasal discharge.
An Otolaryngologist evaluation and diagnosis of chronic inflammatory rhinosinusitis (hyperplastic mucosa, polyps in absence of overt bacterial infection)
Access to telephone (home or person cell).
Exclusion Criteria:
Sinus surgery within the last 3 months
Acute illness within the last 2 weeks requiring antibiotics: including: otitis media, pharyngitis, bronchitis, or laryngitis.
Immunosuppression (due to medications including oral steroids, or due to autoimmune diseases, HIV infection, cystic fibrosis, immunodeficiency, malignancies, uncontrolled diabetes mellitus, chronic renal failure, etc.)
Patients with chronic or acute bacterial sinusitis.(Clinical diagnosis-to be decided by MD)
An allergic reaction to a probiotic dietary supplement in the past (such as symptoms of tightness in the chest, breathing difficulties, skin hives, rash or other clinical symptoms consistent with sensitivity or intolerance)
Inability to speak or read English.
Pregnancy and Lactation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jeffrey E Terrell, MD
Organizational Affiliation
University of Michigan
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Use of Probiotics as Adjunctive Treatment for Chronic Rhinosinusitis
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