COPD
Conditions
Brief summary
Forty five COPD patients will be recruited from Chest Disease Department, Tanta University Hospital, Tanta, Egypt. The aim of the study is to Compare between the effectiveness of three therapeutic options for treatment of moderate and severe COPD patients .These therapeutic options include Inhaled corticosteroid (ICS) plus long acting B2-agonist (LABA) combination, Inhaled corticosteroid (ICS) plus long acting anticholinergic (LAAC) combination and Long acting B2-agonist (LABA) plus long acting anticholinergic (LAAC) combination .
Detailed description
This study will be prospective randomized double blind study. The forty five COPD patients will be divided into three groups: Group 1: 15 patients with COPD who will receive inhaled corticosteroid (ICS)plus long acting B2-agonist (LABA) (Budesonide/Formoterol combination 160/4.5 mcg, 2 inhalations bid ). Group 2: 15 patients with COPD who will receive inhaled corticosteroid (ICS) plus long acting anticholinergic (LAAC) (Tiotropium 18 mcg capsule inhaled once daily + Budesonide ). Group 3: 15 patients with COPD who will receive long acting B2-agonist (LABA) plus long acting anticholinergic (LAAC). If any worsening of dyspnea, increase of purulence, or increase of sputum production appear plus increase of peak variability more than 35% and FEV1 that necessitate a change of the regular drug medication of the patient will be recorded as exacerbation. All patients will be submitted to the following analysis at the baseline, during and 12 weeks after the assigned treatment: 1. Full medical history will be taken through clinical assessment of dyspnea, chronic cough and sputum production using mMRC or CAT test. 2. Forced expiratory volume in 1second (FEV1) value measurement using spirometry. 3. Measurement of the following inflammatory markers in serum and/ or plasma of patients under study . * Tumer necrosis factor alpha ( TNF ) * Fibrinogen * Interlukin 6 ( IL6 ) Statistical analysis The results will be statistically calculated to evaluate its clinical significance if any before ,during and after drug therapy using (ANOVA) system SPSS version 20 (2012) to compare between the three groups of patients and paired t-test will be used to compare between results before, during and after drug therapy .
Interventions
DRUGBudesonide/Formoterol combination 160/4.5 mcg, 2 inhalations bid
inhaled corticosteroid (ICS)plus long acting B2-agonist (LABA) (Budesonide/Formoterol combination 160/4.5 mcg, 2 inhalations bid ).
DRUGTiotropium 18 mcg capsule inhaled once daily + Budesonide
inhaled corticosteroid (ICS) plus long acting anticholinergic (LAAC) (Tiotropium 18 mcg capsule inhaled once daily + Budesonide ).
DRUGFormoterol/Tiotropium
long acting B2-agonist (LABA) plus long acting anticholinergic (LAAC).
Sponsors
Tanta University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Investigator)
Masking description
double blind
Intervention model description
randomized double blind prospective study.
Eligibility
Sex/Gender
ALL
Age
30 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
1. Age from 30 to 40 years or older. 2. Patient with 30%≥ FEV1\<80% predicted and FEV1/FVC \<70% predicted.
Exclusion criteria
1. Patients with FEV1\< 30% predicted or FEV1\< 50% predicted plus chronic respiratory failure. 2. Patients with recent chest infection or had been hospitalised for an exacerbation or respiratory infection in the 6 weeks before screening. 3. Patients with history of asthma. 4. Patient with clinically significant condition ex; unstable ischemic heart disease, uncontrolled hypertension, uncontrolled diabetes.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| FEV1 value | three months | Forced expiratory volume in 1second (FEV1) value |
| Tumer necrosis factor alpha ( TNF ) | three months | serum level |
| Interlukin 6 ( IL6 ) | three months | serum level |
| Fibrinogen | Three months | serum level |
Outcome results
None listed