St. Joseph's Healthcare Hamilton
Hamilton, Ontario, L8N 4A6, Canada
Location status: Recruiting
NCT Number: NCT05086432
In Interstitial Lung Disease (ILD) there is thickening of lung tissue, which makes it difficult for patients to breathe and get enough oxygen into their bodies. In addition to shortness of breath, daily cough is very common, with 4 out of 5 patients experiencing this symptom. Cough in particular has a major impact on the ability to exercise, be active, and to simply enjoy life.
There are many reasons for cough in ILD, and very often there are multiple overlapping causes. It is hard to improve cough in these patients, with available medicines providing limited relief. One explanation for this gap is an incomplete understanding of cough in ILD. To improve patients' cough there is a need to better understand its cause. In other lung diseases, such as asthma, doctors and scientists have used phlegm tests to measure inflammation in the lung, which helps them choose the right medicine for the right patient. This has not been done for ILD, even though it has recently been found that many patients with ILD and everyday cough have abnormal phlegm tests. Using this strategy in ILD could improve patients' cough and quality of life, and possibly even slow progression of the disease.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Hamilton, Ontario, L8N 4A6, Canada
Location status: Recruiting
SpECC-ILD is an open-label, randomized controlled trial assessing the efficacy of sputum-guided management (using sputum cytometry) compared to standard care over 16 weeks in patients with chronic cough and ILD.
A total of 80 participants will be enrolled and randomized in a 1:1 ratio to either sputum guided therapy or standard of care for a total of 16 weeks. Participants randomized to the intervention arm will receive open-label sputum-guided management of airway inflammation identified during screening. Participants in this arm will receive standard of care treatment as determined by their ILD specialist who will be blinded to the results of the sputum analysis.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
As previously described.
As previously described.
Time frame: 16 weeks
The difference in hourly cough frequency over a 24-hour period between baseline and end of study.
Time frame: 16 weeks
The difference in forced expiratory volume in 1 second (as obtained by spirometry) between baseline and end of study
Time frame: 16 weeks
The difference in forced vital capacity (as obtained by spirometry) between baseline and end of study
Time frame: 16 weeks
The difference in LCQ between baseline and end of study
Time frame: 16 weeks
The difference in KB-ILD between baseline and end of study
Time frame: 16 weeks
The difference in sputum total cell count between baseline and end of study
Time frame: 16 weeks
The difference in sputum neutrophil percent between baseline and end of study
Time frame: 16 weeks
The difference in sputum eosinophil percent between baseline and end of study
Time frame: 16 weeks
Adverse events reported by participants
Time frame: 16 weeks
Serious adverse events reported by participants
Time frame: 16 weeks
Rates of completion for bi-weekly LCQ
Time frame: 16 weeks
Rates of adherence to study medications
Contact information is provided by the study sponsor or research team.
McMaster University
Other
Sputum Cytometry Guided Management for the Elimination of Chronic Cough in Patients With Interstitial Lung Disease (SpECC-ILD) - a Randomized Controlled Trial
Acronym: SpECC-ILD
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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