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NCT01013948 · ClinicalTrials.gov registry record

Prevalence of Chronic Airway Obstruction in Subjects With a History of Cigarette Smoking in a Primary Care Setting

A clinical trial, sponsored by GlaxoSmithKline.

Completed
Registry status
1,574
Enrollment target

NCT01013948: Completed study, sponsored by GlaxoSmithKline.

NCT01013948 is a clinical trial that has completed, run by GlaxoSmithKline. The registered enrollment target is 1,574 participants. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01013948 has completed, sponsored by GlaxoSmithKline.

COMPLETED
Registry status
1,574 participants
Enrollment target

Study Summary

This is a cross-sectional study to determine the prevalence of symptomatic airway obstruction using the LFQ as a screening tool in primary care patients with a history of cigarette smoking and to provide descriptive data of this patient population. The study design is multicenter, cross-sectional, and involves a single visit. This study is not intended to evaluate the efficacy or safety of any investigational products. Following completion of written informed consent, eligible study subjects will complete a single study visit encompassing all required study assessments. Study subjects will not receive blinded study medication for evaluations of efficacy and safety. All eligible patients will complete a self-administered Web survey that will include the LFQ. To meet both the primary and secondary aims, all patients with LFQ ≤ 18 (current cut-off for obstruction), as well as 5% of patients who score \> 18, will be candidates for spirometric assessment. Only this subset of patients will undergo pulmonary function tests. Albuterol will be self-administered for determination of post-bronchodilator forced expiratory volume in one-second (FEV1)/forced vital capacity (FVC) ratio and post-bronchodilator FEV1 percentage of predicted normal. The study will end when 800 patients have been assessed spirometrically or 3,000 patients have completed the LFQ (whichever criterion is achieved first). Prior to implementation of the full study, a pilot study will be conducted at two of the chosen study sites to pretest the proposed study procedures.

Interventions

  • OTHER Non-Interventional

Trial Details

FieldValue
Enrollment Target 1,574 participants
Start Date 2009-02
Est. Completion 2009-05
GlaxoSmithKline

1,345 total trials

What the finished NCT01013948 record still lists

NCT01013948 is an observational study that tracks outcomes without assigning an intervention. Its 1,574 participants enrollment target places it among the larger protocols in the corpus.

The record links to 0 conditions, and to 1 intervention - of which Non-Interventional is the first listed.

NCT01013948 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01013948 about?

NCT01013948 is a clinical study titled "Prevalence of Chronic Airway Obstruction in Subjects With a History of Cigarette Smoking in a Primary Care Setting". This is a cross-sectional study to determine the prevalence of symptomatic airway obstruction using the LFQ as a screening tool in primary care patients with a history of cigarette smoking and to provide descriptive data of this patient population. The study design is multicenter, cross-sectional, a...

What is the current status of trial NCT01013948?

This trial is currently completed. The enrollment target is 1,574 participants. The study started on 2009-02. Estimated completion is 2009-05.

What interventions are being tested in trial NCT01013948?

The interventions under investigation include: Non-Interventional (OTHER).

Who is sponsoring clinical trial NCT01013948?

This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.

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Source: ClinicalTrials.gov NCT01013948, the US trial registry maintained by the National Library of Medicine. NCT01013948 (large enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.