RATNO, Reducing Antibiotic Tolerance Using Nitric Oxide in CF - a Phase 2 Pilot Study

University Hospital Southampton NHS Foundation Trust

Status and phase

Completed

Phase 2

Conditions

Cystic Fibrosis

Treatments

Drug: Nitric Oxide

Drug: Control

Study type

Interventional

Funder types

Other

Identifiers

NCT02295566

RHM CHI0548

11/H0502/7 (Other Identifier)

2010-023529-39 (EudraCT Number)

Details and patient eligibility

About

The lungs of most patients with cystic fibrosis (CF) become chronically infected with bacteria called Pseudomonas aeruginosa during childhood. This infection is now known to consist of free-living bacteria (known as "planktonic bacteria") and bacteria in colonies on body surfaces known as "biofilms". The bacteria in biofilms are more resistant and tolerant to antibiotics. Current CF treatment of exacerbations aims to eradicate or control pseudomonal infection using aggressive antibiotic regimes.

Despite this treatment many patients develop chronic infection which is never cleared. Chronic infection causes damage to the lungs. Patients colonised with Pseudomonas are more unwell and die at a younger age. Our laboratory has established that low dose nitric oxide (NO) can disrupt pseudomonal biofilms in the laboratory. This pilot study will discover whether non-toxic levels of NO administered to participants during an episode of acute infection (exacerbation) will disrupt bacteria from biofilms and increase the effectiveness of antibiotic therapy. This protocol describes a participant-blind randomised controlled pilot study of treatment with nitric oxide gas during an acute infective exacerbation (also known simply as an "acute exacerbation"). Patients with CF aged 12 or above will be asked to take part.

They will be randomised to receive 7 days either of inhaled nitric oxide gas or placebo alongside standard therapy during an exacerbation. Sputum samples will be obtained before, during and after the treatment period for microbiological analysis. The primary endpoint will be the microbiological effect on bacterial biofilms before and after NO adjunctive therapy. Secondary microbiological endpoints will include the between group differences in pseudomonal colony forming units (CFU"s), biofilm NO levels and detailed characterisation of biofilms before and after treatment.

Secondary clinical endpoints will include lung function and well-established indicators quality of life. The aim of this randomised pilot study is as proof of concept and to guide the design of a large multi-centre trial to definitively evaluate the effectiveness of NO or NO donors as adjunctive therapy in CF.

Full description

Not required

Enrollment

12 patients

Sex

All

Ages

12+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Adolescents and young adults with cystic fibrosis aged 12 or above
Colonised with Pseudomonas aeruginosa (confirmed on sputum sample)

Exclusion criteria

Colonisation with Burkholderia cepacia
Known hypersensitivity to the antibiotics used in the study
Other known contraindications to the antibiotics to be used in the study including known aminoglycoside related hearing/renal damage
Patients requiring non-invasive ventilation (NIV)
Patients who have a pneumothorax
Patients who are admitted for specific treatment of nontuberculous mycobacteria (NTM)
Patients who cannot tolerate nasal cannula e.g. those who cannot breathe through their nose
Patients who have nasal polyposis that is causing significant blockage of the nasal passages
Adolescents who are not Gillick competent (and therefore not able to give their own assent in addition to parental consent)
Patients not likely to survive the time period of the study washout period (4 months from enrolment)
Treatment with an investigational drug or device within the last 3 months prior to enrolment
Patients who are pregnant (a pregnancy test will be carried out for females of 11 years and above as is standard practice for clinical trials)
Immediate families of investigators or site personnel directly affiliated with the study. Immediate family is defined as child or sibling, whether biological or legally adopted.