Belfast Regional Adult CF Centre
Belfast, BT9 7AE, United Kingdom
NCT Number: NCT04016571
Cystic fibrosis (CF) is a multisystem disease characterized by viscid secretions in multiple organ systems. Lung infection and damage account for most of the disease burden. Acute changes in respiratory signs and symptoms termed Pulmonary Exacerbations require treatment with intravenous antibiotics and hospital admission. These episodes cause substantial disruption to people's lives and impact on lung function, quality of life and lifespan. Current treatment regimes require improvement but further study is needed to identify who might benefit from a different approach.
This observational study aims to assess if multi-dimensional measurements taken during treatment correspond with later treatment response. This may allow us to personalise treatment more effectively in the future and to better understand how individuals respond to treatment.
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Notify Me18 year and older
All sexes
Observational
Belfast, BT9 7AE, United Kingdom
Pulmonary Exacerbations in CF require treatment with intravenous (IV) antibiotics and hospital admission for between 10-21 days. These episodes cause substantial disruption to people's lives and impact on lung function, quality of life and lifespan.Robust evidence to support current treatment approaches is lacking with awareness that current regimes could be optimised.
As yet there is no model for predicting how patients with CF will respond to IV antibiotic treatment- other than clinical judgement and lung function response.This is due to lack of robust measures to identify clinical response at the time of treatment and safely predict later clinical outcomes. The heterogeneity of the 21st Century CF population means a multi-dimensional composite measure is needed. This study has therefore been designed to provide an overall picture of people's response including clinical, biochemical and patient related outcome measures. Using multi-dimensional assessment we hope the measures assessed in this study will give a better picture of how people feel and how they respond to treatment.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Change in lung function between baseline and day 0, Day 5 and Day 14 of treatment
Lung function Measure
Time frame: Need for a further course of IV antibiotics within 30 days of treatment completion
The number of participants requiring a further course of IV antibiotics within 30 days
Time frame: Change between Day 0, day 5 and day 14 of treatment
Change in Respiratory Symptoms assessed by CF-Respiratory Symptom Diary
Time frame: Change between Day 0, day 5 and day 14 of treatment
Change in Physical Activity Levels measured by consumable wearable device
Time frame: Change between Day 0, day 5 and day 14 of treatment
Change in time in bed, time asleep and time awake/restless (mins)
Time frame: Change between Day 0, day 5 and day 14 of treatment
Change in serum inflammatory marker (CRP)
Time frame: Change between Day 0, day 5 and day 14 of treatment
Change in sputum (Interleukins, Tumour Necrosis Factor-Alpha, Calprotectin and Human Mobility Growth Box Protein -1) inflammatory markers (measured in pg/ml)
Time frame: Change between Day 0, day 5 and day 14 of treatment
Change in microbiological growth measured by culture
Time frame: Change between Day 0, day 5 and day 14 of treatment
Change in microbiological relative abundance, dominance, evenness, diversity and richness
Time frame: Change between Day 0, day 5 and day 14 of treatment
Change in 24 hour sputum volume (mls)
Time frame: Time to next course of intravenous antibiotics within 12 month follow up period (study end)
Time to next exacerbation
Belfast Health and Social Care Trust
Other
Acronym: PRIVATE
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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