CClinicalTrials.gg
CompletedNCT01169727Updated May 31, 2012

Observational Study to Evaluate Health Status of Chronic Obstructive Pulmonary Disease (COPD) Patients in Response to Real-life Treatments in Thailand

An observational study in Chronic Obstructive Pulmonary Disease, sponsored by AstraZeneca. Completed at 20 sites in Thailand. Open to participants aged 41 Years and older. Per ClinicalTrials.gov, last updated 2012-05-31.

Sponsored by AstraZeneca · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
684
Ages
41 Years and older
Sex
All
01

Study summary

The purpose of this study is to evaluate health status of uncontrolled Chronic Obstructive Pulmonary Disease (COPD) patients in response to treatments in clinical practice.

Read the detailed description

MC MD

02

Conditions studied

  • Chronic Obstructive Pulmonary Disease

Keywords

  • COPD and CCQ score
  • Changes in PEF,overall CCQ score
03

In context

Lung Diseases

3,303 studies on the registry are indexed under Lung Diseases; 355 are open to participants now.

This study's enrollment of 684 is above the median of 157 across 929 observational studies indexed under Lung Diseases.

Browse Lung Diseases studies →

Lead sponsor

AstraZeneca is the lead sponsor of 3,429 studies on the registry; 270 are open to participants now.

Of its 357 completed or terminated interventional studies of FDA-regulated products, 173 (48%) have results posted.

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

04

Who can participate

Ages eligible
41 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Primary care and Specialty care in 20 centers nationwide in Thailand

Inclusion criteria

  1. Provision of informed consent prior to any study specific procedures
  2. Male or non-pregnant female aged >40 years
  3. A clinical diagnosis of COPD with FEV1/ FVC \<0.70 and require combination or modified therapy
  4. Smoke > 10 Pack Year

Exclusion criteria

Exclusion Criteria:

  1. Involvement in the planning and/or conduct of the study (applies to both AstraZeneca staff and/or staff at the study site)
  2. Participation in a clinical study (precluding non-interventional study or registry) during the last 3 months
05

Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
684 participants (actual)
06

What researchers measure

Primary outcomes

  1. Changes in PEF and overall CCQ score

    Time frame: between the first visit and after 12 (plus or minus 1) weeks

Secondary outcomes

  1. Difference of the changes of PEF and overall CCQ score comparing between various treatments

    Time frame: between the first visit and after 12 (plus or minus 1) weeks

07

Study locations

20 sites
  • Research Site
    SaiMai, Bangkok, Thailand
  • Research Site
    Watana, Bangkok, Thailand
  • Research Site
    Maung, Chantaburi, Thailand
  • Research Site
    Maung, Chiang Mai, Thailand
  • Research Site
    Maung, Chiang Rai, Thailand
  • Research Site
    Muang, Chonburi, Thailand
  • Research Site
    Muang, Khon Kaen, Thailand
  • Research Site
    Ongkharak, Nakhon Nayok, Thailand
  • Research Site
    Maung, Nakhon Sri Thammarat, Thailand
  • Research Site
    Maung, Nakhonratchasima, Thailand
  • Research Site
    Maung, Nakhonsawan, Thailand
  • Research Site
    Maung, Nonthaburi, Thailand
  • Research Site
    Muang, Phitsanulok, Thailand
  • Research Site
    Maung, Phuket, Thailand
  • Research Site
    Maung, Rayong, Thailand
  • Research Site
    Maung, Sakolnakorn, Thailand
  • Research Site
    Hat Yai, Songkla, Thailand
  • Research Site
    Song Phi Nong, Suphan Buri, Thailand
  • Research Site
    Maung, Trang, Thailand
  • Research Site
    Prannok, Bangkok, Thailand
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 31, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01169727
Lead sponsor
AstraZeneca
Responsible party
Sponsor
First posted
Jul 26, 2010
Start date
Jul 2010
Primary completion
Mar 2012
Completion
Mar 2012
Last update
May 31, 2012

Study contacts

Assoc. Prof. Watchara Boonsawat
principal investigator · Khon Kaen University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in May 2012. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion