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Comparative Study of Lung Bioavailability of HFA-Seretide Via Current Spacer Devices in Healthy Volunteers

Primary Purpose

Asthma

Status
Completed
Phase
Phase 4
Locations
United Kingdom
Study Type
Interventional
Intervention
Seretide 250(8puffs) via Evohaler actuator
Seretide 250 (8 puffs)/placebo via Volumatic spacer
Seretide 250/placebo 8 puffs via Aerochamber Plus spacer
Seretide 250/placebo via Synchro-Breathe
Sponsored by
Brian J Lipworth
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Asthma focused on measuring lung bioavailability, asthma, seretide, Spacer

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Healthy Volunteers
  2. Male or female 18-65
  3. Informed Consent
  4. Ability to comply with the requirements of the protocol

Exclusion Criteria:

  1. No respiratory disease
  2. Smokers
  3. Recent respiratory tract infection (2 months).
  4. Any other clinically significant medical condition such as unstable angina, acute myocardial infarction in the preceding 3 months, recent TIA/ CVA,that may endanger the health or safety of the participant, or jeopardise the protocol.
  5. Any significant abnormal laboratory result as deemed by the investigators
  6. Pregnancy, planned pregnancy or lactation
  7. Known or suspected contra-indication to any of the IMP's
  8. Concomitant use of medicines (prescribed, over the counter or herbal) that may interfere with the trial

Sites / Locations

  • Asthma & Allergy Research Group, Department of cardiovascular & lung biology, Division of medicine, Ninewells Hospital & Medical School

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

Experimental

Experimental

Arm Label

Evohaler

Volumatic spacer

Aerochamber Plus

Synchro-Breathe

Arm Description

Outcomes

Primary Outcome Measures

Overnight Urinary Cortisol creatinine ratio
This outcome measure evaluates the amount of cortisol being suppressed after inhaled steroid administration. This helps to assess the systemic effect of steroid inhalation and therefore the propensity for adrenal suppression which is a noted adverse effect with high dose inhaled steroids

Secondary Outcome Measures

Serum Potassium
The serum potassium is monitored 60 minutes post study drug inhalation to assess the systemic beta-2-adrenoreceptor metabolic response. Long acting beta agonists like Salmeterol exhibit dose related reduction in serum potassium.

Full Information

First Posted
September 2, 2010
Last Updated
April 10, 2019
Sponsor
Brian J Lipworth
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1. Study Identification

Unique Protocol Identification Number
NCT01194700
Brief Title
Comparative Study of Lung Bioavailability of HFA-Seretide Via Current Spacer Devices in Healthy Volunteers
Official Title
Comparative Study of Lung Bioavailability of HFA-Seretide Via Current Spacer Devices in Healthy Volunteers
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
November 2009 (undefined)
Primary Completion Date
December 2009 (Actual)
Study Completion Date
December 2009 (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
The purpose of this study is to determine the effect of plastic spacers and breath actuated spacers on respirable drug delivery of combination steroid inhaler (Seretide/Advair) and whether electrostatic charge within plastic spacers has a clinically relevant impact on the inhaled steroid delivery.
Detailed Description
Conventional plastic spacers are bulky and can be influenced by electrostatic charge, which can reduce respirable dose delivery especially when used brand new "out of the box". Breath actuated integrated vortex spacer (Synchro-Breathe) is a compact palm sized antistatic device with a vortex chamber which is designed to be more patient friendly and free from the effects of electrostatic charge. The systemic bioavailability from the lung of inhaled fluticasone and salmeterol is dependent on respirable dose delivery, and hence the performance of inhaler devices can be quantified by measuring the degree of adrenal suppression and fall in serum potassium(K) as surrogates for delivered lung dose. This study attempts to compares the systemic bioavailability from the lung in real life conditions for Fluticasone/Salmeterol combination (measured in terms of relative adrenal suppression and fall in serum K) via the breath actuated Synchro-Breathe device, pMDI( Seretide Evohaler), and Aerochamber Plus & Volumatic spacer used brand new "out of the box" in healthy volunteers.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Asthma
Keywords
lung bioavailability, asthma, seretide, Spacer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
19 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Evohaler
Arm Type
Experimental
Arm Title
Volumatic spacer
Arm Type
Experimental
Arm Title
Aerochamber Plus
Arm Type
Experimental
Arm Title
Synchro-Breathe
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Seretide 250(8puffs) via Evohaler actuator
Other Intervention Name(s)
Advair
Intervention Description
8 puffs of Seretide250/Placebo via Evohaler actuator
Intervention Type
Drug
Intervention Name(s)
Seretide 250 (8 puffs)/placebo via Volumatic spacer
Other Intervention Name(s)
Advair
Intervention Description
8 puffs of Seretide 250/placebo via volumatic spacer
Intervention Type
Drug
Intervention Name(s)
Seretide 250/placebo 8 puffs via Aerochamber Plus spacer
Other Intervention Name(s)
Advair
Intervention Description
Seretide 250/placebo 8 puffs via Aerochamber Plus
Intervention Type
Drug
Intervention Name(s)
Seretide 250/placebo via Synchro-Breathe
Other Intervention Name(s)
Advair
Intervention Description
Seretide 250/placebo 8puffs via breath actuated Synchro-Breathe device
Primary Outcome Measure Information:
Title
Overnight Urinary Cortisol creatinine ratio
Description
This outcome measure evaluates the amount of cortisol being suppressed after inhaled steroid administration. This helps to assess the systemic effect of steroid inhalation and therefore the propensity for adrenal suppression which is a noted adverse effect with high dose inhaled steroids
Time Frame
within 24 hours after study drug inhalation
Secondary Outcome Measure Information:
Title
Serum Potassium
Description
The serum potassium is monitored 60 minutes post study drug inhalation to assess the systemic beta-2-adrenoreceptor metabolic response. Long acting beta agonists like Salmeterol exhibit dose related reduction in serum potassium.
Time Frame
60 minutes post treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy Volunteers Male or female 18-65 Informed Consent Ability to comply with the requirements of the protocol Exclusion Criteria: No respiratory disease Smokers Recent respiratory tract infection (2 months). Any other clinically significant medical condition such as unstable angina, acute myocardial infarction in the preceding 3 months, recent TIA/ CVA,that may endanger the health or safety of the participant, or jeopardise the protocol. Any significant abnormal laboratory result as deemed by the investigators Pregnancy, planned pregnancy or lactation Known or suspected contra-indication to any of the IMP's Concomitant use of medicines (prescribed, over the counter or herbal) that may interfere with the trial
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Arun Nair
Organizational Affiliation
University of Dundee
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Brian J Lipworth
Organizational Affiliation
University of Dundee
Official's Role
Study Director
Facility Information:
Facility Name
Asthma & Allergy Research Group, Department of cardiovascular & lung biology, Division of medicine, Ninewells Hospital & Medical School
City
Dundee
State/Province
Tayside
ZIP/Postal Code
DD1 9SY
Country
United Kingdom

12. IPD Sharing Statement

Citations:
PubMed Identifier
21240480
Citation
Nair A, McKinlay L, Williamson P, Short P, Burns P, Lipworth BJ. Comparative lung bioavailability of fluticasone/salmeterol via a breath-actuated spacer and conventional plastic spacers. Eur J Clin Pharmacol. 2011 Apr;67(4):355-363. doi: 10.1007/s00228-010-0989-9. Epub 2011 Jan 15. Erratum In: Eur J Clin Pharmacol. 2017 Jun;73(6):793.
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Comparative Study of Lung Bioavailability of HFA-Seretide Via Current Spacer Devices in Healthy Volunteers

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