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Recruiting Observational

Correlation of Inflammatory Markers and Radiological Findings in Stable Bronchiectasis Patients With Exacerbation Phenotype

NCT07495982 · tracked via the Priya Life Science Egypt tracker
Phase
Observational
Started
2025-11-01
Last updated
2026-03-27

Condition(s) studied

Correlation of Inflammatory Markers and Radiological Findings in Stable Bronchiectasis Patients

Investigational drug(s) / intervention(s)

Inflammatory Markers and Radiological Findings

Inflammatory Markers and Radiological Findings: 1. Functional assessment: the available functional assessment will be performed. 2. Laboratory: CBC, neutrophil: lymphocyte ratio (NLR), platelet : lymphocyte ratio (PLR), C-reactive protein (CRP), ESR, renal and liver function, serum albumin level. 3. Microbiology: Sputum Gram stain, culture and sensitivity when indicated. 4. Radiology: High Resolution CT chest with lobar assessment and severity scoring (Reiff, Bhalla, BRICS).

Study summary

Bronchiectasis, also referred to as non-cystic fibrosis (non-CF) bronchiectasis, is a chronic respiratory disease defined by abnormal and irreversible dilatation of the bronchi (1). Dilatation of the bronchial lumen predisposes to infection (2). Recurrent infection and airway inflammation leads to tissue damage and inflammation that leads to excess mucus production and delayed mucociliary clearance, predisposing the patient to recurrent and chronic infections (3). This in turn creates a cycle of further tissue damage and infection (4), leading to recurrent exacerbations, hospitalizations and loss of lung function. Non-CF bronchiectasis patients who experience frequent exacerbations (≥2 per year) represent a high-risk group with accelerated disease progression.Bronchiectasis has become a major health concern due to its increasing prevalence and associated healthcare costs (5). The disease can be caused by many different etiologies, which may be causative, synergistic, or coincidental, depending on the manner in which they interact and it is clinically characterized by a variety of symptoms, including cough, sputum production and airway infection, and can often present with recurrent exacerbations (6). An exacerbation is generally defined as a sustained clinical deterioration characterized by an increase in symptoms, which may include increased cough, increased sputum volume or change in consistency, increased sputum purulence (color change), increased breathlessness and/or reduced exercise tolerance, increased fatigue and/or malaise, hemoptysis for at least 48 h requiring a change in treatment.

Recurrent exacerbations are related to elevated systemic and airway inflammation, deterioration of lung function and progression of the disease(7). In addition to known etiologies of bronchiectasis, several other diseases may occur at any stage of bronchiectasis and are likely major contributors to increased hospitalizations, healthcare utilization and socioeconomic costs. These include cardiovascular disorders, gastro-oesophageal reflux disease (GORD), psychological illnesses, pulmonary hypertension, cognitive impairment, and lung, oesophageal and hematological malignancies (8-9).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * adult patients (≥18 years) with non-cystic fibrosis bronchiectasis confirmed by High Resolution Computed Tomography (HRCT). Exclusion Criteria: * Patients with cystic fibrosis-related bronchiectasis. * Patients with active pulmonary tuberculosis. * Patients with chronic debilitating diseases e.g. advanced hepatic or renal diseases. * Patients with primary autoimmune or malignancy requiring immunosuppressive therapy at the time of the marker measurement. * Patients refusing participation.

Primary outcome measure(s)

  • Correlation of the inflammatory markers and radiological findings with exacerbation phenotype. — 1/11/2026

Trial sites (1)

FacilityCityRegionStatus
Faculty of medicine Sohag Egypt Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07495982 on ClinicalTrials.gov ↗ ← All trials in Egypt