The Effect of Twice Daily vs. Once Daily Bronchodilation on Hyperinflation in COPD Patients During 24 Hours.

NCT ID: NCT03275116

Last Updated: 2020-03-10

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE4
• Total Enrollment: 49 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-07-07
• Study Completion Date: 2020-12-31

Brief Summary

To study the effect of twice daily dual bronchodilation versus once daily single bronchodilation in patients with chronic obstructive pulmonary disease on 24-hour static and dynamic hyperinflation.

Detailed Description

To study the effect of twice daily dual bronchodilation (Aclidinium Bromide/Formoterol Fumarate 340/12 mcg) versus once daily single bronchodilation (Tiotropium 'respimat' 5 mcg) in patients with COPD on 24-hour static and dynamic hyperinflation, spirometry respiratory symptoms and sleep quality.

Conditions

Chronic Obstructive Airway Disease

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: CROSSOVER
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Twice daily dual bronchodilation

Twice daily Aclidinium Bromide/Formoterol Fumarate 340/12 mcg during 4 days

Group Type: ACTIVE_COMPARATOR

Tiotropium 'Respimat' 5 mcg

Intervention Type: DRUG

Once daily single bronchodilation

Once daily single bronchodilation

Once daily Tiotropium 'Respimat' 5 mcg during 4 days

Group Type: ACTIVE_COMPARATOR

Aclidinium Bromide/Formoterol Fumarate 340/12 mcg

Intervention Type: DRUG

Twice daily dual bronchodilation

Interventions

Tiotropium 'Respimat' 5 mcg

Once daily single bronchodilation

Intervention Type: DRUG

Aclidinium Bromide/Formoterol Fumarate 340/12 mcg

Twice daily dual bronchodilation

Intervention Type: DRUG

Other Intervention Names

Spiriva 'Respimat'; Duaklir Genuair

Eligibility Criteria

Inclusion Criteria

1. Male and female adults (with an equal sex ratio not exceeding 35-65%) aged ≥ 40 years with written informed consent obtained prior to any study-related procedure.

2. Patients entering pulmonary rehabilitation at CIRO.

3. Patients with a diagnosis of moderate to very severe COPD at least 12 months before the screening visit (A post-bronchodilator FEV1 < 80% of the predicted normal value and a post-bronchodilator FEV1/FVC < 0.7 at least 10-15 min after 4 puffs (4 x 100 μg) of salbutamol)

4. Patients with severe static hyperinflation defined as residual volume (body box) > 150 % predicted.

5. Current smokers or ex-smokers with a smoking history of at least 10 pack years [pack-years = (number of cigarettes per day x number of years)/20].

6. MMRC (modified Medical Research Council Dyspnea scale) score ≥ 2.

7. A cooperative attitude and ability to use correctly the inhalers. ICS (inhalation corticosteroids) use is not an exclusion criterion for participation in the study and will be continued during the study. During the study, patients receive fluticasone in an equivalent dose of their own regimen.

The use of neomacrolides and/or leukotriene antagonists is not an exclusion criterion for participation in the study and will be continued in the study, as long as there are no changes in the regiments in the 4 weeks prior to the study. Also, the use of corticosteroid maintenance therapy is allowed, provided that no changes in the regiments took place in the 4 weeks prior to study.

Exclusion Criteria

1. Pregnant or lactating women and all women physiologically capable of becoming pregnant (i.e. women of childbearing potential)

2. Patients requiring use of the following medications:

1. A course of systemic steroids longer than 3 days for COPD exacerbation in the 4 weeks prior to screening.

2. A course of antibiotics for COPD exacerbation longer than 7 days in the 4 weeks prior to screening. NB; maintenance treatment of macrolides is allowed, without any changes in the regimen in the 4 weeks prior to the study.

3. PDE4 (phosphodiesterase-4) inhibitors in the 4 weeks prior to screening.

4. Xanthines in the 4 weeks prior to screening.

5. Use of antibiotics for a lower respiratory tract infection (e.g pneumonia) in the 4 weeks prior to screening.

3. COPD exacerbation requiring prescriptions of systemic corticosteroids and/or antibiotics or hospitalization during the run-in period.

4. Patients treated with non-cardio selective β-blockers in the month preceding the screening visit or during the run-in period. Those patients may enter the study after non-selective β-blockers withdrawal and/or cardio selective β-blockers intake for at least 10 days before the first study day.

5. Patients treated with long-acting antihistamines unless taken at stable regimen at least 2 months prior to screening and to be maintained constant during the study, or if taken as PRN (Pro Re Nata).

6. Patients requiring long term (at least 12 hours daily) oxygen therapy for chronic hypoxemia.

7. Known respiratory disorders other than COPD which may impact the efficacy of the study drug according the investigator's judgment. This can include but is not limited to alpha-1 antitrypsin deficiency, active tuberculosis, a history of asthma, lung cancer, bronchiectasis, sarcoidosis, lung fibrosis, pulmonary hypertension and interstitial lung disease.

8. Previous lung surgery or endoscopic lung volume reduction interventions.

9. Patients who have clinically significant cardiovascular condition such as, but not limited to, unstable ischemic heart disease, NYHA Class III/IV left ventricular failure, acute ischemic heart disease in the last year prior to study screening, history of sustained cardiac arrhythmias or sustained and non-sustained cardiac arrhythmias diagnosed in the last 6 months (sustained means lasting more than 30 seconds and or ending only with external action, and or leads to hemodynamic collapse; non-sustained means > 3 beats < 30 seconds, and or ending spontaneously, and or asymptomatic), impulse conduction high degree blocks, patients with Implantable Cardioverter Defribrillator (ICD).

10. Patients with atrial fibrillation (AF):

1. Paroxysmal Atrial Fibrillation

2. Persistent: AF episode either lasts longer than 7 days or requires termination by cardioversion, either with drugs or by direct current cardioversion (DCC) within 6 months from screening.

3. Long standing persistent as defined by continuous atrial fibrillation diagnosed for less than 6 months with or without a rhythm control strategy.

4. Permanent: for at least 6 months with a resting ventricular rate ≥ 100/min controlled with a rate control strategy (i.e., selective β-blocker, calcium channel blocker, pacemaker placement, digoxin or ablation therapy).

11. An abnormal and clinically significant 12-lead ECG which may impact the safety of the patient according to investigator's judgement. Patients whose electrocardiogram (ECG12 lead) shows QTcF >450 ms for males or QTcF >470 ms for females at screening visit are not eligible (not applicable for patient with pacemaker).

12. Medical diagnosis of narrow-angle glaucoma, prostatic hypertrophy or bladder neck obstruction that in the opinion of the investigator would prevent use of anticholinergic agents.

13. History of hypersensitivity to anticholinergics, β2-agonist or any of the excipients contained in any of the formulations used in the trial which may raise contra-indications or impact the efficacy of the study drug according to the investigator's judgement.

14. Clinically significant laboratory abnormalities indicating a significant or unstable concomitant disease which may impact the efficacy or the safety of the study drug according to investigator's judgement.

15. Patients with hypokalaemia (serum potassium levels <3.5 mEq/L (or 3.5 mmol/L)) or uncontrolled hyperkalaemia according to investigator's judgment.

16. Unstable concurrent disease: e.g. uncontrolled hyperthyroidism, uncontrolled diabetes mellitus or other endocrine disease; significant hepatic impairment; significant renal impairment; uncontrolled gastrointestinal disease (e.g. active peptic ulcer); uncontrolled neurological disease; uncontrolled haematological disease; uncontrolled autoimmune disorders, or other which may impact the efficacy or the safety of the study drug according to investigator's judgment.

17. Patients with any history of malignancy likely to result in significant disability or likely to require significant medical or surgical intervention within the next six months (after V1) or with malignancy for which they are currently undergoing radiation therapy or chemotherapy.

18. History of alcohol abuse and/or substance/drug abuse within 12 months prior to screening visit.

19. Participation in another clinical trial where investigation drug was received less than 8 weeks prior to screening visit.

• Minimum Eligible Age: 40 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Center for Integrated Rehabilitation and Organ Failure Horn

OTHER

Sponsor Role: collaborator

AstraZeneca

INDUSTRY

Sponsor Role: collaborator

Maastricht University Medical Center

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Lowie Vanfleteren, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

CIRO, centre of expertise for chronic organ failure

Locations

Ciro, center of expertise in chronic organ failure

Horn, , Netherlands

Site Status: RECRUITING

Countries

Netherlands

Central Contacts

Lowie Vanfleteren, MD, PhD

Role: CONTACT

lowievanfleteren@ciro-horn.nl

+31475587644

Maud Koopman, MD

Role: CONTACT

maudkoopman@ciro-horn.nl

+31475587653

Facility Contacts

Maud Koopman, MD

Role: primary

maudkoopman@ciro-horn.nl

+31475587653

Other Identifiers

59452

Identifier Type: -

Identifier Source: org_study_id