Nasal Microbiota Transfer Therapy in Chronic Rhinosinusitis Without Nasal Polyps (CRSsNP)

Last updated: November 30, 2023
Sponsor: The University of Queensland
Overall Status: Active - Recruiting

Phase

N/A

Condition

Sinusitis

Rhinitis, Allergic, Perennial

Polyps

Treatment

Microbiome Transplant

Placebo

Clinical Study ID

NCT05400616
University of Queensland
  • Ages 18-80
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

Chronic Rhinosinusitis (CRS) is a chronic inflammatory condition of the nasal passage and paranasal sinuses that places significant burden on affected patients and global healthcare systems.

Current treatments for CRS such as long-term antibiotics, anti-inflammatory drugs, and surgery often reduce symptoms and signs of disease temporarily, however long-term results are much less satisfactory.

Recently, the theory of a damaged microbiome (dysbiosis) as a cause or promoting factor behind CRS has gained increasing evidence from the scientific community.

A condition of the gut with microbial dysbiosis (c.difficile) has previously employed microbiota transplant treatment with great success in long-term health outcomes. Such treatments are shown to repopulate bacterial microenvironment and restore protective commensal bacterial load.

A pilot study conducted by this study team trialed a novel intervention of a Nasal Microbiota Transplant in a small group of participants. Preliminary results suggested significantly improved CRS symptoms after treatment with a healthy donor microbiota transplant, compared to the pre-transplant baseline. The addition of a randomized-control trial with inclusion of a placebo group is the next step.

In this study, investigators aim to perform a two-arm, double-blinded, phase II randomized controlled clinical trial in order to assess the efficacy of a Nasal Microbiota Transplant against a placebo in a cohort of CRS patients without Nasal Polyps (CRSsNP).

Eligibility Criteria

Inclusion

Inclusion criteria (patient):

  • Diagnosis of Chronic Rhinosinusitis as defined by the presence of 2 or more majorsinonasal symptoms (nasal blockage, nasal discharge, loss of smell, and facial pain/fullness) for a minimum of 12 weeks
  • Endoscopic confirmation of middle meatus inflammation or presence of mucopurulence,and /or CT confirmation of paranasal sinus inflammation.
  • Previous nasal surgery with patent ostia to the diseased ethmoids and maxillarysinuses
  • Signed written informed consent Inclusion criteria (donor):
  • No history of sinonasal or lower airway disease for the last 2 years other than thecommon cold.
  • No clinical findings of sinonasal disease at the inclusion visit.
  • Accepted as a donor by the patient.
  • Signed informed consent to participate in the study.

Exclusion

Exclusion Criteria: Exclusion criteria (patient):

  • Aged <18 or >80 years
  • Allergy to amoxicillin or clavulanate potassium and Clarithromycin.
  • Excessive Nasal polyposis
  • Antibiotic treatment in the last 4 weeks
  • Patients with a history supporting a diagnosis of immune deficiency will be tested (Immunoglobulin A (IgA), Immunoglobulin M (IgM), Immunoglobulin G (IgG) and IgGsubclasses, MBL) and /or are immunocompromised due to disease and / or medication (e.g., insulin dependent diabetes mellitis, systemic corticosteroids)
  • Patients who live with someone who is severly immunocompromised.
  • Patients with cystic fibrosis or ciliary dyskinesia
  • Patients who have been on an active investigational therapy within 2 months ofscreening
  • Patients who have clinically significant laboratory abnormalities
  • Patients who are pregnant, breast feeding or planning to become pregnant during thestudy
  • Patients who are not willing to use a double barrier method of contraception duringthe study that is:-
  1. females must use contraceptive pill or Intra-uterine device (IUD) or similar andcondoms
  2. males must use condoms and spermicidal gel
  • Patients currently on any medication that may affect the results in an unpredictablemanner
  • The patient does not agree to comply with or is unable to meet all study requirementsfor the duration of the study period
  • Patients deemed by the investigator to be unsuitable for participation in the study
  • Patients who have had Coronavirus-19 (COVID-19) within the last month. Exclusion criteria (donor):
  • Findings in the prestudy pathogen scan that makes the donor unsuitable. Prestudypathogen scan: Prior to first donation, the donors will be tested for HIV, HumanT-lymphotropic virus 1 and 2, Hepatitis B and C, Syphilis, Tuberculosis, HerpesSimplex (HSV 1 and 2), Varicella Zoster (VZV), Cytomegalovirus (CMV), Epstein-Barrvirus (EBV), Methicillin-resistant Staphylococcus aureus (MRSA) and a standard panelfor sinonasal pathogens (Pneumococci, H. Influenza, Beta-streptococci and M.Catarrhalis).
  • Donors who have had COVID-19 within the last 2 months.
  • If the donor is positive for Herpes Simplex, CMV or EBV they will be consideredunsuitable as a donor for a patient negative for the same pathogen. If the donor ispositive for any other pathogen they will be considered unsuitable as a donorentirely.

Study Design

Total Participants: 60
Treatment Group(s): 2
Primary Treatment: Microbiome Transplant
Phase:
Study Start date:
November 10, 2022
Estimated Completion Date:
December 31, 2025

Study Description

Current treatments for CRS such as long-term antibiotics, anti-inflammatory drugs, and surgery often reduce symptoms and signs of disease temporarily, however long-term results are much less satisfactory.

A microbiota therapy, as an alternative treatment to antibiotics, has the potential of improving outcomes for CRS patients long-term, whilst reducing the use of antibiotics in the community.

Several attempts of studies to define the role of microbiota of the nose and paranasal sinuses in health and disease have not yet been able to achieve a universal consensus. This is in part due to the significant inter-individual microbiota variation and complexity within humans. Such challenges have also limited the use of probiotic assemblages of one or a combination of few bacterial species in treatment of CRS.

The data derived from this study will add to our understanding of the role of the microbiome in the airways and its role in interfering with respiratory pathogens and host immunity. This is likely to have implications for CRS microbiome-based therapies, and also other potentially related respiratory conditions such as asthma, and chronic obstructive pulmonary disease (COPD).

In this study, investigators will recruit patients suffering from chronic rhinosinusitis without polyps (CRSsNP) and healthy participants that do not have a history of sinonasal disease. The sinus microbiome transplants will occur over a 2 week period, with regular follow up for up to 6-months post intervention. Main outcomes include change in disease severity, symptom severity, inflammatory changes, and microbial composition across the study period. Successful results from this trial may pave the way for a novel therapeutic for CRS patients.

This study has received ethics approval from the Royal Brisbane and Women's Health Human Resource and Ethics Committee (RBWH HREC).

Connect with a study center

  • Royal Brisbane and Women's Hospital

    Brisbane, Queensland 4006
    Australia

    Active - Recruiting

  • University of Queensland

    Brisbane, Queensland 4680
    Australia

    Site Not Available

  • Monash Health

    Melbourne,
    Australia

    Site Not Available

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