Sinonasal Microbiome Transplant as a Therapy for Chronic Rhinosinusitis Without Nasal Polyps (CRSsNP)
Primary Purpose
Chronic Rhinosinusitis (Diagnosis)
Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Microbiome transplant
Sponsored by
About this trial
This is an interventional treatment trial for Chronic Rhinosinusitis (Diagnosis)
Eligibility Criteria
Inclusion criteria (patient)
- 2 nasal symptoms: 1 of which must be nasal obstruction or discoloured discharge.
- Sinusitis verified by endoscopy or CT-scan.
- Duration > 12 weeks.
- Previous surgery with patent ostia to the diseased sinuses.
- Signed informed consent to participate in the study.
Inclusion criteria (donor)
- No history of sinonasal or lower airway disease within the last 2 years other than the common cold.
- Accepted as a donor by the patient.
- Signed informed consent to participate in the study.
Exclusion criteria (patient)
- Nasal polyposis.
- Antibiotic treatment within the last 4 weeks.
- On-going or recent participation in another clinical trial.
- Any medication that may affect the results in an unpredictable manner.
- Immune deficiency.
- Allergy to amoxicillin or clavulanate potassium and clarithromycin.
- Pregnancy or breastfeeding.
Exclusion criteria (donor)
- Chronic rhinosinusitis.
- Acute rhinosinusitis within the last two years.
- Nasal polyposis.
- Asthma.
- Antibiotic treatment within the last 4 weeks.
- On-going or recent participation in another clinical trial.
- Clinical findings of sinonasal disease at the inclusion visit.
- Findings in the pre-study pathogen scan that makes the donor unsuitable.
- Pregnancy or breastfeeding.
Sites / Locations
- Departement of ORL
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Microbiome transplant
Arm Description
The only arm of the study. Patients suffering from CRSsNP gets microbiome transplants from donors without any sinonasal health problems.
Outcomes
Primary Outcome Measures
SNOT-22
Change of burden of disease as measured by the SNOT-22 (22 item sinonasal outcome test) questionnaire in patients
Secondary Outcome Measures
Lund Kennedy endoscopy score
Grading of burden of disease as measured using the Lund-Kennedy endoscopy score.
Subjective symptom score
Subjective scoring of symptoms related to sinonasal, lower airway, intestinal and other
Inflammatory burden
Amount of inflammatory mediators collected in nasal lavages.
Microflora
Change in nasal microflora measured using both culture dependant and non culture dependant microbiological techniques.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03122795
Brief Title
Sinonasal Microbiome Transplant as a Therapy for Chronic Rhinosinusitis Without Nasal Polyps (CRSsNP)
Official Title
Sinonasal Microbiome Transplant as a Therapy for Chronic Rhinosinusitis Without Nasal Polyps (CRSsNP)
Study Type
Interventional
2. Study Status
Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
May 15, 2017 (Actual)
Primary Completion Date
December 17, 2018 (Actual)
Study Completion Date
December 31, 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Region Skane
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Chronic rhinosinusitis (CRS) is a disease associated with impaired quality of life and substantial societal costs. Though sometimes co-appearing with other conditions, such as asthma, allergy, and nasal polyps, many cases present without co-morbidities. Micro-biological diagnostic procedures are frequently undertaken, but the results are often inconclusive. Nevertheless, antibiotics are usually prescribed, but invariably with limited and temporary success. Accordingly, there is a need for new treatments for CRS.
Recent studies indicate that the sinuses are colonized by a commensal microbiome of bacteria and that damage to this natural microbiome, by pathogens or antibiotics, may cause an imbalance that may promote CRS. Therefore, treatments that restore the commensal microbiome may offer an alternative to current protocols. Arguably, as suggested by studies on patients with intestinal infections (next paragraph), one such possibility may be to transfer a "normal microbiome" to patients with CRS.
A disrupted microbiome is linked to intestinal clostridium difficile infections. Probiotic restitution therapy may be effective even in cases recalcitrant to antibiotic treatment. However, a key to effective probiotic restitution is selecting the bacteria that facilitate regrowth of normal microbiome. As an answer to this, researchers have chosen to simply transplant the entire microbiome from a healthy donor. In the case of clostridium difficile infection in the form of faecal transplants.
In this study, we will examine the possibility to treat patients with chronic rhinosinusitis without polyps (CRSsNP) with complete sinonasal microbiomes obtained from healthy donors. Our analysis will focus on symptoms and signs of disease as well as on nasal inflammatory and microbiological indices.
Detailed Description
Over the last few years the theory of a damaged microbiome as a cause or promoting factor behind chronic rhinosinusitis has gained increasing interest from the scientific community.
A number of studies aimed at investigating the microbiota of the nose and paranasal sinuses in health and disease has been published with very varying outcomes. Furthermore, other studies have been aimed at probiotic treatment of sinonasal disease either locally or through immunologic manipulation via the gastrointestinal microbiota.
A problem common to all these studies is that studies examining the normal nasal microbiota have identified a great amount of different bacterial species. It is as of today not known which individual species or combinations of species that promotes health.
The probiotic assemblages examined in previous studies have consisted of one or a combination of a few bacterial species.
Probiotic restitution therapy has been proven very effective for intestinal clostridium difficile infections. The restitution therapy has then consisted of transplantation of a complete microbiome from a healthy donor in the form of a faecal transplant.
In this study the investigators aim at recruiting patients suffering from chronic rhinosinusitis without polyps (CRSsNP) and healthy participants without any history sinonasal disease. The patients and the healthy participants will be examined for infectious diseases in a manner similar to other medical transplant procedures to minimize the risk for the recipients. The patients will then be treated with antibiotics to reduce the bacterial load of the nose and the paranasal sinuses. After the patient has finished the antibiotic treatment a microbiome transplant will be harvested from the healthy participant as a nasal lavage. The raw lavage fluid will then be used to transplant the microbiome to the patient. The procedure will be repeated for five consecutive days.
The outcome measures analysed will focus on subjective sinonasal health and symptoms of the patients but also include nasal inflammatory and microbiological indices.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Rhinosinusitis (Diagnosis)
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Patients and donors who meet the inclusion criteria will be recruited and inclueded and put through the study in a cumulative fashion.
Masking
None (Open Label)
Allocation
N/A
Enrollment
22 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Microbiome transplant
Arm Type
Experimental
Arm Description
The only arm of the study. Patients suffering from CRSsNP gets microbiome transplants from donors without any sinonasal health problems.
Intervention Type
Procedure
Intervention Name(s)
Microbiome transplant
Intervention Description
A raw microbiome, collected from a donor without any sinonasal health problems, as a nasal lavage.
Primary Outcome Measure Information:
Title
SNOT-22
Description
Change of burden of disease as measured by the SNOT-22 (22 item sinonasal outcome test) questionnaire in patients
Time Frame
Day 1 to day 106
Secondary Outcome Measure Information:
Title
Lund Kennedy endoscopy score
Description
Grading of burden of disease as measured using the Lund-Kennedy endoscopy score.
Time Frame
Day 1 to day 106
Title
Subjective symptom score
Description
Subjective scoring of symptoms related to sinonasal, lower airway, intestinal and other
Time Frame
Day 1 to 106.
Title
Inflammatory burden
Description
Amount of inflammatory mediators collected in nasal lavages.
Time Frame
Day 1 to day 106
Title
Microflora
Description
Change in nasal microflora measured using both culture dependant and non culture dependant microbiological techniques.
Time Frame
Day 1 to day 106
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion criteria (patient)
2 nasal symptoms: 1 of which must be nasal obstruction or discoloured discharge.
Sinusitis verified by endoscopy or CT-scan.
Duration > 12 weeks.
Previous surgery with patent ostia to the diseased sinuses.
Signed informed consent to participate in the study.
Inclusion criteria (donor)
No history of sinonasal or lower airway disease within the last 2 years other than the common cold.
Accepted as a donor by the patient.
Signed informed consent to participate in the study.
Exclusion criteria (patient)
Nasal polyposis.
Antibiotic treatment within the last 4 weeks.
On-going or recent participation in another clinical trial.
Any medication that may affect the results in an unpredictable manner.
Immune deficiency.
Allergy to amoxicillin or clavulanate potassium and clarithromycin.
Pregnancy or breastfeeding.
Exclusion criteria (donor)
Chronic rhinosinusitis.
Acute rhinosinusitis within the last two years.
Nasal polyposis.
Asthma.
Antibiotic treatment within the last 4 weeks.
On-going or recent participation in another clinical trial.
Clinical findings of sinonasal disease at the inclusion visit.
Findings in the pre-study pathogen scan that makes the donor unsuitable.
Pregnancy or breastfeeding.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anders Mårtensson, MD
Organizational Affiliation
Region Skåne
Official's Role
Principal Investigator
Facility Information:
Facility Name
Departement of ORL
City
Helsingborg
ZIP/Postal Code
25187
Country
Sweden
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Data will be presented at group level for personal integrity reasons.
Citations:
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Sinonasal Microbiome Transplant as a Therapy for Chronic Rhinosinusitis Without Nasal Polyps (CRSsNP)
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