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Effectiveness of Antibiotic Therapy for Exacerbations of Chronic Obstructive Pulmonary Disease (TRANCE)

Primary Purpose

Chronic Obstructive Pulmonary Disease

Status
Completed
Phase
Phase 4
Locations
Spain
Study Type
Interventional
Intervention
Placebo
Amoxicillin and clavulanic acid
Sponsored by
Catalan Society of Family Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Obstructive Pulmonary Disease focused on measuring COPD, Antibiotics

Eligibility Criteria

40 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Acute exacerbations (at least one criterion present: increase of dyspnoea, increase of sputum production and/or increase of purulence) of
  • patients older than 40 years old,
  • smokers or ex-smokers of more than 10 pack-years,
  • with COPD and FEV1 greater than 50%, diagnosed by spirometry and a predicted ratio FEV1/FVC<0.7%.

Exclusion Criteria:

  • Severe COPD (FEV1<50%)
  • Pneumonia
  • Active neoplasm
  • Tracheotomy
  • Criteria for hospitalisation
  • Patients previously being on antibiotics
  • Immunodepressed patients
  • History of hypersensitivity to beta-lactams or intolerance to clavulanate
  • Enrollment in other clinical trials
  • Patients who refuse to take part in this study
  • Patients who have not had a spirometry test for the past two years

Sites / Locations

  • Hospital Clínic
  • Primary Healthcare Center La Marina
  • Primary Healthcare Center Figueres
  • Primary Healthcare Center Montilivi
  • Primary Healthcare Center Girona-4
  • Primary Healthcare Centre Breda-Hostalric
  • Primary Healthcare Center Lleida
  • Primary Healthcare Centre Molins de Rei
  • Primary Healthcare Centre Olot
  • Primary Healthcare Center Reus-3
  • Primary Healthcare Center Les Muralles
  • Primary Healthcare Centre Jaume I
  • Primary Healthcare Center Valls Urbà

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Placebo

Amoxycillin and clavulanic acid

Arm Description

Placebo pills t.i.d. for 8 days

Amoxycillin and clavulanate t.i.d. for 8 days

Outcomes

Primary Outcome Measures

Number of Patients Who Were Cured
Cure defined as the disappearance of the acute signs and symptoms related to the infection, with complete return to the previous situation of stability

Secondary Outcome Measures

Number of Days Till the Next Exacerbation
For the assessment of the time till next exacerbation patients were monitored over a period of 365 days on a three-monthly basis. Patients were instructed to contact their physician immediately if there was any change in their health status. Diagnosis of a new exacerbation was based on the same clinical criteria described previously. For the calculation of time to the next exacerbation, all clinical failures occurring during therapy were counted as zero exacerbation-free interval days.

Full Information

First Posted
July 2, 2007
Last Updated
March 11, 2012
Sponsor
Catalan Society of Family Medicine
Collaborators
Fondo de Investigacion Sanitaria
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1. Study Identification

Unique Protocol Identification Number
NCT00495586
Brief Title
Effectiveness of Antibiotic Therapy for Exacerbations of Chronic Obstructive Pulmonary Disease
Acronym
TRANCE
Official Title
Situations That do Not Require Antibiotics for Acute Exacerbations of Mild-to-moderate Chronic Obstructive Pulmonary Disease
Study Type
Interventional

2. Study Status

Record Verification Date
March 2012
Overall Recruitment Status
Completed
Study Start Date
October 2007 (undefined)
Primary Completion Date
July 2010 (Actual)
Study Completion Date
July 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Catalan Society of Family Medicine
Collaborators
Fondo de Investigacion Sanitaria

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to determine the effectiveness of antibiotic therapy for patients with acute exacerbations of mild-to-moderate chronic obstructive pulmonary disease.
Detailed Description
Antibiotics are usually prescribed for acute exacerbations of chronic obstructive pulmonary disease (COPD) even though their benefit in mild-to-moderate COPD is not demonstrated. The aim of this study is to assess the effectiveness of antibiotic therapy for exacerbations of COPD, what clinical variables are associated with an improved clinical response with antibiotic therapy with respect to placebo and to identify which patients might recover from an acute exacerbation without antibiotic therapy. Methodology: prospective, randomised, double blind, placebo-controlled clinical trial, in which exacerbations (at least one criterion present: increase of dyspnoea, increase of sputum production and/or increase of purulence) of patients older than 40 yr., smokers or ex-smokers of more than 10 pack-years, with COPD and FEV1 greater than 50%, diagnosed by spirometry and a predicted ratio FEV1/FVC<0.7%. Exclusion criteria: severe COPD (FEV1<50%), active neoplasm, tracheotomy, pneumonia, hospitalization criteria, patients previously being on antibiotics, immunodepressed, history of hypersensitivity to beta-lactams or intolerance to clavulanate, enrollment in other clinical trials, patients who refuse to take part in this study, and patients who have not had a spirometry test for the past two years. Sample size: 677 patients. Interventions: first visit: the patient will be given details of the clinical trial and will be asked to sign informed consent; other data: sputum color, chest X-ray ordered to rule out pneumonia, C-reactive protein levels, and peak flow measurement. The patient will be randomised to receive amoxicillin plus clavulanate or placebo and will be scheduled to return for a 2nd follow-up visit after 3 or 4 days to assess the clinical response and peak flow measurements and to rule out any worsening of the condition. Third visit: scheduled after 9-11 days to assess the clinical response, drug-compliance and peak flow measurement. Fourth visit after 15-20 days for clinical assessment and to observe whether any relapses have occurred. Date of the following exacerbation will be recorded.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease
Keywords
COPD, Antibiotics

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
318 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo pills t.i.d. for 8 days
Arm Title
Amoxycillin and clavulanic acid
Arm Type
Active Comparator
Arm Description
Amoxycillin and clavulanate t.i.d. for 8 days
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
It's placebo
Intervention Description
One pill to be taken every eight hours for 8 days
Intervention Type
Drug
Intervention Name(s)
Amoxicillin and clavulanic acid
Other Intervention Name(s)
Augmentine 500-125 mg 24 pills
Intervention Description
500-125 mg to be taken every eight hours for 8 days
Primary Outcome Measure Information:
Title
Number of Patients Who Were Cured
Description
Cure defined as the disappearance of the acute signs and symptoms related to the infection, with complete return to the previous situation of stability
Time Frame
Day 9-11
Secondary Outcome Measure Information:
Title
Number of Days Till the Next Exacerbation
Description
For the assessment of the time till next exacerbation patients were monitored over a period of 365 days on a three-monthly basis. Patients were instructed to contact their physician immediately if there was any change in their health status. Diagnosis of a new exacerbation was based on the same clinical criteria described previously. For the calculation of time to the next exacerbation, all clinical failures occurring during therapy were counted as zero exacerbation-free interval days.
Time Frame
One year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Acute exacerbations (at least one criterion present: increase of dyspnoea, increase of sputum production and/or increase of purulence) of patients older than 40 years old, smokers or ex-smokers of more than 10 pack-years, with COPD and FEV1 greater than 50%, diagnosed by spirometry and a predicted ratio FEV1/FVC<0.7%. Exclusion Criteria: Severe COPD (FEV1<50%) Pneumonia Active neoplasm Tracheotomy Criteria for hospitalisation Patients previously being on antibiotics Immunodepressed patients History of hypersensitivity to beta-lactams or intolerance to clavulanate Enrollment in other clinical trials Patients who refuse to take part in this study Patients who have not had a spirometry test for the past two years
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carl Llor, Doctor
Organizational Affiliation
Catalan Society of Family Medicine
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Marc Miravitlles, Doctor
Organizational Affiliation
Hospital Clinic
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Ana Moragas, Family doc.
Organizational Affiliation
Catalan Society of Family Medicine
Official's Role
Study Director
Facility Information:
Facility Name
Hospital Clínic
City
Barcelona
State/Province
Catalonia
ZIP/Postal Code
08036
Country
Spain
Facility Name
Primary Healthcare Center La Marina
City
Barcelona
State/Province
Catalonia
ZIP/Postal Code
08038
Country
Spain
Facility Name
Primary Healthcare Center Figueres
City
Figueres
State/Province
Catalonia
ZIP/Postal Code
17600
Country
Spain
Facility Name
Primary Healthcare Center Montilivi
City
Girona
State/Province
Catalonia
ZIP/Postal Code
17003
Country
Spain
Facility Name
Primary Healthcare Center Girona-4
City
Girona
State/Province
Catalonia
ZIP/Postal Code
17007
Country
Spain
Facility Name
Primary Healthcare Centre Breda-Hostalric
City
Hostalric
State/Province
Catalonia
ZIP/Postal Code
17450
Country
Spain
Facility Name
Primary Healthcare Center Lleida
City
Lleida
State/Province
Catalonia
ZIP/Postal Code
25001
Country
Spain
Facility Name
Primary Healthcare Centre Molins de Rei
City
Molins de Rey
State/Province
Catalonia
ZIP/Postal Code
08750
Country
Spain
Facility Name
Primary Healthcare Centre Olot
City
Olot
State/Province
Catalonia
ZIP/Postal Code
17800
Country
Spain
Facility Name
Primary Healthcare Center Reus-3
City
Reus
State/Province
Catalonia
ZIP/Postal Code
43203
Country
Spain
Facility Name
Primary Healthcare Center Les Muralles
City
Tarragona
State/Province
Catalonia
ZIP/Postal Code
43003
Country
Spain
Facility Name
Primary Healthcare Centre Jaume I
City
Tarragona
State/Province
Catalonia
ZIP/Postal Code
43005
Country
Spain
Facility Name
Primary Healthcare Center Valls Urbà
City
Valls
State/Province
Catalonia
ZIP/Postal Code
43600
Country
Spain

12. IPD Sharing Statement

Citations:
PubMed Identifier
23807094
Citation
Miravitlles M, Moragas A, Hernandez S, Bayona C, Llor C. Is it possible to identify exacerbations of mild to moderate COPD that do not require antibiotic treatment? Chest. 2013 Nov;144(5):1571-1577. doi: 10.1378/chest.13-0518.
Results Reference
derived
PubMed Identifier
22923662
Citation
Llor C, Moragas A, Hernandez S, Bayona C, Miravitlles M. Efficacy of antibiotic therapy for acute exacerbations of mild to moderate chronic obstructive pulmonary disease. Am J Respir Crit Care Med. 2012 Oct 15;186(8):716-23. doi: 10.1164/rccm.201206-0996OC. Epub 2012 Aug 23.
Results Reference
derived

Learn more about this trial

Effectiveness of Antibiotic Therapy for Exacerbations of Chronic Obstructive Pulmonary Disease

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