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NCT Number: NCT05086432

Sputum Cytometry Guided Management for the Elimination of Chronic Cough in Patients With ILD

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

St. Joseph's Healthcare Hamilton

Hamilton, Ontario, L8N 4A6, Canada

Location status: Recruiting

Location contact

Terence Ho, MB MSc

CONTACT

[email protected]

905-522-1155 ext. Ext. 32995

Terence Ho, MB MSc

PRINCIPAL_INVESTIGATOR

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Written informed consent consistent with ICH-GCP and local laws, signed prior to any study procedures being performed
  • Age >18 years
  • A clinical diagnosis of ILD with accepted specific diagnoses including:
  • Idiopathic pulmonary fibrosis (IPF)
  • Chronic hypersensitivity pneumonitis associated ILD (CHP-ILD)
  • Connective tissue disease associated ILD (CTD-ILD)
  • Pneumoconiosis
  • Daily Cough for at least 8 weeks
  • Able to produce an adequate sample with sputum induction

Exclusion criteria

  • Patients with a diagnosis of systemic sclerosis associated ILD (SSc-ILD) or sarcoidosis
  • Cause of cough attributed to a known etiology (ex. ACE-inhibitor, uncontrolled gastroesophageal reflux or upper airway cough syndrome, acute viral illness)
  • Current use of inhaled corticosteroids
  • Current use of systemic corticosteroids (prednisone equivalent > 20mg/day)
  • Current use of chronic antibiotics
  • Airflow obstruction (ie. pre-bronchodilator FEV1/FVC ratio < 0.7)
  • History of physician-diagnosed asthma
  • History of emphysema
  • A history of cholestatic jaundice or hepatic dysfunction associated with prior use of azithromycin
  • Moderate to severe hepatic dysfunction with a Child Pugh score >10
  • Known allergy or hypersensitivity to inhaled corticosteroids or macrolide antibiotics
  • Corrected QT-interval (QTc) on screening electrocardiogram (ECG) of > 450ms
  • An established history of untreated atypical mycobacterial infection
  • A history of hearing impairment, tinnitus, or vertigo
  • Medication use likely to suppress cough (ex: morphine, gabapentin, amitriptyline)

Treatment and study plan

Sputum-guided management

Other

As previously described.

Standard of care

Other

As previously described.

Primary outcomes

  1. Change in hourly cough frequency

    Time frame: 16 weeks

    The difference in hourly cough frequency over a 24-hour period between baseline and end of study.

Secondary outcomes

  1. Change in FEV1

    Time frame: 16 weeks

    The difference in forced expiratory volume in 1 second (as obtained by spirometry) between baseline and end of study

  2. Change in FVC

    Time frame: 16 weeks

    The difference in forced vital capacity (as obtained by spirometry) between baseline and end of study

  3. Change in Leicester Cough Questionnaire

    Time frame: 16 weeks

    The difference in LCQ between baseline and end of study

  4. Change in King's Brief ILD Questionnaire

    Time frame: 16 weeks

    The difference in KB-ILD between baseline and end of study

  5. Change in sputum total cell count

    Time frame: 16 weeks

    The difference in sputum total cell count between baseline and end of study

  6. Change in sputum neutrophils

    Time frame: 16 weeks

    The difference in sputum neutrophil percent between baseline and end of study

  7. Change in sputum eosinophils

    Time frame: 16 weeks

    The difference in sputum eosinophil percent between baseline and end of study

  8. Adverse events

    Time frame: 16 weeks

    Adverse events reported by participants

  9. Serious adverse events

    Time frame: 16 weeks

    Serious adverse events reported by participants

  10. Completion rates for Bi-weekly LCQ

    Time frame: 16 weeks

    Rates of completion for bi-weekly LCQ

  11. Study medication adherence rate

    Time frame: 16 weeks

    Rates of adherence to study medications

Study contacts

Contact information is provided by the study sponsor or research team.

Ciaran Scallan, MB

CONTACT

[email protected]

9055221155 ext. 34330

Terence Ho, MB, MSc

CONTACT

[email protected]

9055221155 ext. 32995

Sponsors and collaborators

Lead sponsor

McMaster University

Other

Collaborators

  • St. Joseph's Healthcare Hamilton
  • Vitalograph

Registry information

Official study title

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

Important dates

Study start
2025
Primary completion
2027
Study completion
2027
First posted
Oct 20, 2021
Registry last updated
Sep 29, 2025

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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