Formoterol Via pMDI HFA-134a Propellant or DPI in Partially Reversible Chronic Obstructive Pulmonary Disease (COPD)

NCT00742248 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 54

Last updated 2020-07-31

No results posted yet for this study

Summary

The purpose of this study is to demonstrate equivalent efficacy between two different formulations of formoterol (pMDI using HFA-134 propellant and dry powder) on lung function in adult patients with partially reversible COPD.

Conditions

Interventions

DRUG

Formoterol

pMDI 12 mcg/dose 1 dose in the morning and 1 dose in the evening

DRUG

Formoterol

DPI 12 mcg/dose 1 dose in the morning and 1 dose in the evening

DRUG

Placebo

Placebo pMDI/DPI 1 dose in the morning and 1 dose in the evening

Sponsors & Collaborators

  • Vito Brusasco "Centro Dipartimentale di Fisiopatologia Respiratoria", University of Genoa, Italy (Co-ordinating centre)

    collaborator UNKNOWN
  • Giovanni Barisione "Unità Operativa di Medicina Preventiva e del Lavoro, Laboratorio di Fisiopatologia Respiratoria", S. Martino Hospital, Genoa, Italy

    collaborator UNKNOWN
  • Universita degli Studi di Genova

    collaborator OTHER
  • Cardarelli Hospital

    collaborator OTHER
  • Roberto Dal Negro "Unità Operativa di Pneumologia", Hospital of Bussolengo (Verona), Italy

    collaborator UNKNOWN
  • University of Modena and Reggio Emilia

    collaborator OTHER
  • Carlo Mereu "Struttura complessa di Pneumologia", S. Corona Hospital, Pietra Ligure (Savona), Italy

    collaborator UNKNOWN
  • University of Pisa

    collaborator OTHER
  • Fondazione Don Carlo Gnocchi Onlus

    collaborator OTHER
  • Chiesi Farmaceutici S.p.A.

    lead INDUSTRY

Principal Investigators

  • Giovanni Barisione, MD · "Unità Operativa di Medicina Preventiva e del Lavoro, Laboratorio di Fisiopatologia Respiratoria", S. Martino Hospital, Genoa, Italy

  • Giorgio Canonica, MD · 3) "Clinica di Malattie dell'Apparato Respiratorio e Allergologia, Dipartimento di Medicina Interna", University of Genoa, Italy

  • Gennaro D'Amato, MD · 'Unita' di Pneumologia e Allergologia, Dipartimento di Medicina Respiratoria', A. Cardarelli Hospital, Naples, Italy

  • Roberto Dal Negro, MD · 5) "Unità Operativa di Pneumologia", Hospital of Bussolengo (Verona), Italy

  • Leonardo Fabbri, MD · "Clinica di Malattie dell'Apparato Respiratorio", University of Modena, Italy

  • Carlo Mereu, MD · "Struttura complessa di Pneumologia", S. Corona Hospital, Pietra Ligure (Savona), Italy

  • Pierluigi Paggiaro, MD · "Servizio di Fisiopatologia Respiratoria, Dipartimento Cardiotoracico", University of Pisa, Italy

  • Giorgio Scano, MD · "Unità Operativa di Riabilitazione Respiratoria, Fondazione Don Carlo Gnocchi ONLUS", Pozzolatico (FI), Italy

  • Vito Brusasco, MD, PhD · "Centro Dipartimentale di Fisiopatologia Respiratoria", University of Genoa, Italy (Co-ordinating centre)

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
CROSSOVER

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-09-30
Primary Completion
2005-05-31
Completion
2005-05-31

Countries

  • Italy

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00742248 on ClinicalTrials.gov