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Differential Trough Effects of 'Triple Therapy' on Pulmonary Function in Chronic Obstructive Pulmonary Disease (COPD) (FARD12)

Primary Purpose

COPD

Status
Completed
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
Budesonide/formoterol and tiotropium
Budesonide/formoterol and placebo
Sponsored by
Brian J Lipworth
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for COPD focused on measuring COPD (chronic obstructive pulmonary disease)

Eligibility Criteria

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

Inclusion Criteria:

  • Current or ex-smokers
  • aged over 50years
  • FEV1/FVC ratio less than 0.7
  • FEV1 less than 60% predicted

Exclusion Criteria:

  • Diagnosis of asthma, ABPA or bronchiectasis
  • Recent RTI or steroid use
  • Inability to perform study procedures or to give informed consent
  • Known sensitivity to trial medications

Sites / Locations

  • Asthma and Allergy Research Group, Ninewells Hospital and Medical School

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Triple therapy

Combination therapy

Arm Description

Symbicort and tiotropium

Symbicort and placebo

Outcomes

Primary Outcome Measures

Change in trough FEV1 for tiotropium compared to placebo when added to formoterol/budesonide combination

Secondary Outcome Measures

Change in IOS and bodyplethysmography at trough for tiotropium compared to placebo when added to formoterol/budesonide combination
Change in spirometry, IOS and Bodyplethysmography at trough for formoterol/budesonide compared to washed-out baseline

Full Information

First Posted
October 15, 2009
Last Updated
April 10, 2019
Sponsor
Brian J Lipworth
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1. Study Identification

Unique Protocol Identification Number
NCT00996697
Brief Title
Differential Trough Effects of 'Triple Therapy' on Pulmonary Function in Chronic Obstructive Pulmonary Disease (COPD)
Acronym
FARD12
Official Title
A Proof Of Concept Study To Evaluate Tiotropium as Add-on Therapy to Inhaled Budesonide/Formoterol Combination in COPD
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
October 2006 (undefined)
Primary Completion Date
September 2008 (Actual)
Study Completion Date
September 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Brian J Lipworth

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Different medications are often used in combination for the condition COPD (chronic obstructive pulmonary disease). Some medicines act by opening the airways (bronchodilators) and some act as anti-inflammatories (steroids). More recently an approach of using a combination inhaler (containing a steroid and a long-acting bronchodilator) at the same time as a long acting bronchodilator of a different group of medicines (anti-cholinergics inhalers) has been used. This approach is sometimes called 'triple therapy'. Studies which have looked at these combinations usually use only standard blowing tests (spirometry) to test these medicines and focus on the effects of the medicines at their highest (peak) levels. It is some ways more relevant to study these medicines towards to end of the dose period (trough)- just before the next dose. This is when there is less medicine in the system, and differences in drug effects are more obvious. There are also more detailed breathing tests than spirometry which get a more detailed picture of the way the lungs respond to bronchodilator medicines. The investigators have studied 'triple therapy' in COPD, by measuring the effects at the end of the dosing interval (trough) using a range of detailed respiratory tests.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
COPD
Keywords
COPD (chronic obstructive pulmonary disease)

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Triple therapy
Arm Type
Active Comparator
Arm Description
Symbicort and tiotropium
Arm Title
Combination therapy
Arm Type
Placebo Comparator
Arm Description
Symbicort and placebo
Intervention Type
Drug
Intervention Name(s)
Budesonide/formoterol and tiotropium
Intervention Description
Symbicort 200/2, 2puff bid plus tiotropium 18mcg/day
Intervention Type
Drug
Intervention Name(s)
Budesonide/formoterol and placebo
Intervention Description
Symbicort 200/6 2puff bid and placebo
Primary Outcome Measure Information:
Title
Change in trough FEV1 for tiotropium compared to placebo when added to formoterol/budesonide combination
Time Frame
2 weeks
Secondary Outcome Measure Information:
Title
Change in IOS and bodyplethysmography at trough for tiotropium compared to placebo when added to formoterol/budesonide combination
Time Frame
2 weeks
Title
Change in spirometry, IOS and Bodyplethysmography at trough for formoterol/budesonide compared to washed-out baseline
Time Frame
4 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Current or ex-smokers aged over 50years FEV1/FVC ratio less than 0.7 FEV1 less than 60% predicted Exclusion Criteria: Diagnosis of asthma, ABPA or bronchiectasis Recent RTI or steroid use Inability to perform study procedures or to give informed consent Known sensitivity to trial medications
Facility Information:
Facility Name
Asthma and Allergy Research Group, Ninewells Hospital and Medical School
City
Dundee
State/Province
Tayside
ZIP/Postal Code
DD1 9SY
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
20418370
Citation
Williamson PA, Short PM, Clearie KL, Vaidyanathan S, Fardon TC, Howaniec LJ, Lipworth BJ. Paradoxical trough effects of triple therapy with budesonide/formoterol and tiotropium bromide on pulmonary function outcomes in COPD. Chest. 2010 Sep;138(3):595-604. doi: 10.1378/chest.10-0247. Epub 2010 Apr 23.
Results Reference
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Differential Trough Effects of 'Triple Therapy' on Pulmonary Function in Chronic Obstructive Pulmonary Disease (COPD)

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