Berodual® Respimat® vs Metered Dose Inhaler in Patients With Chronic Obstructive Pulmonary Disease

Pulmonary Disease, Chronic Obstructive Clinical Trial

Official title:

A Randomised Open Label, Four Way, Cross-over Scintigraphic Evaluation of the Respimat® Inhaler vs a Metered Dose Inhaler (HFA-MDI) Using Berodual® in Patients With Chronic Obstructive Pulmonary Disease (COPD) With Poor MDI Technique

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02176187
• Other study ID #: 215.1360
• Status: Terminated
• Phase: Phase 3
• First received: June 24, 2014
• Last updated: July 11, 2014
• Start date: April 2003

Study information

• Verified date: July 2014
• Source: Boehringer Ingelheim
• Contact: n/a
• Is FDA regulated: No
• Health authority: United Kingdom: Medicines and Healthcare Products Regulatory Agency
• Study type: Interventional

Clinical Trial Summary

Study to compare the effect of 'natural' as opposed to 'optimal' technique on the percentage of the dose received from the Respimat® inhaler and metered dose inhaler

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 3
• Est. primary completion date: December 2004
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• All patients must have a diagnosis of COPD and must meet the following spirometric criteria:

• Patients must have relatively stable, mild to severe airway obstruction with an forced expiratory volulme in one second (FEV1) =70% of predicted normal and FEV1 =70% of forced vital capacity (FVC). Predicted normal values calculated according to evolutionary conserved chromosome segments (ECCS)

• Patients who have frequent exacerbations which could be expected to interfere with the patient's ability to participate in the study should be excluded

• Male or non-pregnant/non-lactating female patients aged =18 years

• Patients must demonstrate poor MDI technique prior to the start of the study. Presence of any of the following will be considered poor technique:

• Failure to co-ordinate "firing" of an MDI with inhalation

• Too fast an inhalation rate (> 30 litres/minute (L/min))

• Presence of "Cold Freon" effect (MDI spray hitting the back of the throat that caused the patient to stop inhaling)

• All patients must sign an informed consent form prior to participation in the study, i.e. prior to pre-study washout of their usual pulmonary medications

• Current or ex-smokers with a smoking history of >10 pack years

Exclusion Criteria:

• Patients with significant diseases other than COPD will be excluded. A significant disease is defined as a disease which in the opinion of the investigator may either put the patient at risk because of participation in the study or a disease which may influence the results of the study or the patient's ability to participate in the study

• Patients with clinically relevant abnormal baseline haematology, blood chemistry or urinalysis, if the abnormality defines a disease listed as an exclusion criterion will be excluded

• Patients with a recent history (i.e. six months or less) of myocardial infarction

• Patients with any unstable or life-threatening cardiac arrhythmia or who have been hospitalised for heart failure within the past year

• Patients who regularly use daytime oxygen therapy for more than 1 hour per day and in the investigator's opinion will be unable to abstain from the use of oxygen

• Patients with known active tuberculosis

• Patients with a history of cancer within the last five years. Patients with treated basal cell carcinoma are allowed

• Patients with a history of life-threatening pulmonary obstruction, or a history of cystic fibrosis or bronchiectasis

• Patients who have undergone thoracotomy with pulmonary resection. Patients with a history of thoracotomy for other reasons should be evaluated as per exclusion 1

• Patients with any upper respiratory infection in the past 14 days prior to the screening visit or during the baseline period

• Patients who are currently in a pulmonary rehabilitation programme or who have completed a pulmonary rehabilitation programme in the six weeks prior to the screening visit

• Patients with known hypersensitivity to ß2-agonists, anticholinergic drugs or any excipients of the active or placebo Berodual®

• Patients with known narrow-angle glaucoma

• Patients who are being treated with antihistamines (H1 receptor antagonists)

• Patients using oral corticosteroid medication at unstable doses (i.e. less than six weeks on a stable dose) or at doses in excess of the equivalent of 10 mg of prednisolone per day or 20 mg every other day

• Patients who are being treated with monamine oxidase inhibitors or tricyclic antidepressants

• Pregnant or nursing women or women of childbearing potential not using a medically approved means of contraception (i.e. oral or injectable eg Depo-Provera or Noristerat contraceptives, intrauterine devices, diaphragm (plus spermicide) or subdermal implants eg: Norplant®)

• Patients with, in the opinion of the investigator, a history of and/or active significant alcohol or drug abuse

• Patients who have taken an investigational drug within four months or six half lives (whichever is the greater) prior to screening visit and/or the administration of radiolabelled dosage forms within the three months prior to the screening visit

• Radiation exposure from clinical studies, including that from the present study and diagnostic X-rays but excluding background radiation, exceeding 5 millisievert (mSv) in the last 12 months or 10 mSv in the last five years. No patient whose occupational exposure is monitored will participate in the study

Precautions: As with other anticholinergic drugs, Berodual® should be used with caution in patients with prostatic hyperplasia or bladder neck obstruction.

Study Design

Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Chronic Disease
• Lung Diseases
• Lung Diseases, Obstructive
• Pulmonary Disease, Chronic Obstructive

Intervention

Drug:
• Berodual® Respimat® inhaler
fenoterol hydrobromide 50µg + ipratropium bromide 20µg
• Berodual® metered dose inhaler
fenoterol hydrobromide 50µg + ipratropium bromide 20µg

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Boehringer Ingelheim

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percentage of dose in the whole lung	Deposition of aerosol via gamma scintigraphy	immediately after dosing	No
Secondary	Percentage of dose in the central lung zone	Deposition of aerosol via gamma scintigraphy	immediately after dosing	No
Secondary	Percentage of dose in the intermediate lung zone deposition	Deposition of aerosol via gamma scintigraphy	immediately after dosing	No
Secondary	Percentage of dose in the peripheral lung zone deposition	Deposition of aerosol via gamma scintigraphy	immediately after dosing	No
Secondary	Peripheral lung zone/central lung zone deposition ratio (lung penetration index)	Deposition of aerosol via gamma scintigraphy	immediately after dosing	No
Secondary	Percentage of dose in oropharyngeal deposition	Deposition of aerosol via gamma scintigraphy	immediately after dosing	No

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