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CompletedNCT00570544Updated Aug 14, 2008

Tiotropium Induced Bronchodilation in Lung CT Scored Emphysema

An observational study in COPD and Emphysema, sponsored by Gelb, Arthur F., M.D.. Completed at 1 site in United States. Open to participants aged 40 Years to 85 Years. Per ClinicalTrials.gov, last updated 2008-08-14.

Sponsored by Gelb, Arthur F., M.D. · Observational

Study type
Observational
Model
Case-crossover
Time perspective
Retrospective
Enrollment
29
Ages
40 Years to 85 Years
Sex
All
01

Study summary

To evaluate if tiotropium (Spiriva)induced bronchodilation of inspiratory capacity in patients with moderate to severe copd subjected to metronome paced hyperventilation induced dynamic hyperinflation is dependent upon the extent of underlying emphysema as determined by high resolution-thin section CT lung.

Read the detailed description

We will analyze post hoc, data that was previously published: Gelb AF et al.Chest 2006;131:690-695. We have shown that tiotropium increases resting inspiratory capacity thereby providing lung volume protection against metronome paced hyperventilation induced dynamic hyperinflation. End point will be to correlate increase in tiotropium induced FEV 1(L) and inspiratory capacity with extent of underlying emphysema as scored by lung CT ( Gelb AF et al:Chest 1996; 109: 353-359)in 29 patients with COPD. We will also correlate the decrease in inspiratory capacity following metronome paced hyperventilation induced dynamic hyperinflation with extent of lung CT scored emphysema.

02

Conditions studied

  • COPD
  • Emphysema

Keywords

  • copd
  • emphysema
  • tiotropium
  • lung function
  • dynamic hyperinflation
03

In context

Pulmonary Emphysema

187 studies on the registry are indexed under Pulmonary Emphysema; 19 are open to participants now.

This study's enrollment of 29 is below the median of 74 across 48 observational studies indexed under Pulmonary Emphysema.

Browse Pulmonary Emphysema studies →

Lead sponsor

Gelb, Arthur F., M.D. is the lead sponsor of 7 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
40 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

patients with moderate to severe copd from tertiary care pulmonary clinic

Inclusion criteria

  • moderate to severe copd

Exclusion criteria

Exclusion Criteria

  • unable to tolerate tiotropium
  • unable to perform metronome paced hyperventilation induced dynamic hyperinflation
05

Study design

Observational model
Case-crossover
Time perspective
Retrospective
Enrollment
29 participants (actual)

Groups and cohorts

  • 1

    patients with moderate to severe copd with varying extent of emphysema

    Drug: tiotropium

Interventions

  • Drugtiotropium

    18ug capsule daily for 30 days

    Also known as: Spiriva

06

What researchers measure

Primary outcomes

  1. Correlate tiotropium induced increase in inspiratory capacity (IC)and FEV 1 with extent of emphysema as scored by lung CT.

    Time frame: After 30 days and 1.5hr of tiotropium

Secondary outcomes

  1. Correlate decrease in IC and FEV 1 following dynamic hyperinflation with underlying emphysema.

    Time frame: After 30 days and 1.5hr of tiotropium

07

Study locations

1 site
  • Arthur F Gelb Medical Corporation
    Lakewood, California 90712, United States
08

References and documents

Publications

  • Gelb AF, Taylor CF, McClean PA, Shinar CM, Rodrigues MT, Gutierrez CA, Chapman KR, Zamel N. Tiotropium and simplified detection of dynamic hyperinflation. Chest. 2007 Mar;131(3):690-695. doi: 10.1378/chest.06-1662. PubMed 17356081 ↗
  • Gelb AF, Hogg JC, Muller NL, Schein MJ, Kuei J, Tashkin DP, Epstein JD, Kollin J, Green RH, Zamel N, Elliott WM, Hadjiaghai L. Contribution of emphysema and small airways in COPD. Chest. 1996 Feb;109(2):353-9. doi: 10.1378/chest.109.2.353. PubMed 8620705 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 14, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00570544
Lead sponsor
Gelb, Arthur F., M.D.
Collaborators
Boehringer Ingelheim, Pfizer
First posted
Dec 11, 2007
Start date
Aug 2004
Completion
Aug 2005
Last update
Aug 14, 2008

Study contacts

Arthur F Gelb, MD
principal investigator · Arthur F Gelb Medical Corporation

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Dec 2007. You cannot join it, but the record below documents what was studied.

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