Pulmonary Disease, Chronic ObstructiveNCT02236715
Postmarketing Surveillance Study of Atrovent® in Chronic Obstructive Airways Disease
An observational study of Pulmonary Disease, Chronic Obstructive, run by Boehringer Ingelheim.
Trial summary
Study to obtain further information on the tolerability and efficacy of Atrovent® unit dose vial 500 µg in the treatment of Chronic Obstructive Airways Disease under conditions of daily practice Read more about this study
- Who is it for?
- Ages 30 years and older
- Conditions the study is for
- Pulmonary Disease, Chronic Obstructive
- What is being tested?
- Atrovent®
- How many people
- 1,039 participants
- Where
- No sites listed yet
- Study dates
- Sep 1999to Feb 2000
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 30 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Study population: Patients with chronic obstructive airways disease recruited at general practitioners, pneumologists, internists
Who may be able to join
- Primarily patients of both gender, older than 30 years, who suffer from chronic obstructive airways disease
- Only patients who had not been treated with Atrovent® within the last year were to be considered for inclusion
Who cannot join
- Contraindication listed in the instructions for use/summary of product characteristics for Atrovent® unit dose vial 500 µg
About this study
Official title: Postmarketing Surveillance Study (as Per §67(6)AMG[German Drug Law]) of Atrovent® Unit Dose Vial 500 µg in Chronic Obstructive Airways Disease
Study to obtain further information on the tolerability and efficacy of Atrovent® unit dose vial 500 µg in the treatment of Chronic Obstructive Airways Disease under conditions of daily practice
- Conditions
- Pulmonary Disease, Chronic Obstructive
- Being tested
- Atrovent®
- Medical subject headings
- Pulmonary Disease, Chronic Obstructive
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Atrovent®Drug
| Study group | Role | What they receive |
|---|---|---|
| Chronic Obstructive Airways Disease | Not described Receives: Drug: Atrovent® |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in total severity of the clinical picture rated on a 4-point scale
Measured: after 4 weeks
Secondary outcomes (5)
Assessment of efficacy by investigator on a 4-point scale
Measured: after 4 weeks
Assessment of efficacy by patient on a 4-point scale
Measured: after 4 weeks
Assessment of tolerability by investigator on a 4-point scale
Measured: after 4 weeks
Assessment of tolerability by patient on a 4-point scale
Measured: after 4 weeks
Number of patients with adverse drug reactions
Measured: up to 4 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted11 Sep 2014 (estimated)
- Study startSep 1999
- Primary completionFeb 2000
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Pulmonary Disease, Chronic ObstructiveStudies of the same condition, open and under way.
- More trials run by Boehringer IngelheimThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 1,039 participants (actual)
Sponsor and investigators
- Lead sponsor
- Boehringer Ingelheim
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02236715
- Sponsor's protocol ID
- 244.2493
- Status last verified
- Sep 2014
- First submitted
- 10 Sep 2014
- Last updated
- 11 Sep 2014
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 11 Sep 2014. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Postmarketing Surveillance Study (as Per §67(6)AMG[German Drug Law]) of Atrovent® Unit Dose Vial 500 µg in Chronic Obstructive Airways Disease
- ClinicalTrials.gov ID
- NCT02236715
- Acronym / sponsor ID
- 244.2493
- Conditions
- Pulmonary Disease, Chronic Obstructive
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 1,039 participants (actual)
- Lead sponsor
- Boehringer IngelheimIndustry (pharma, biotech, devices)
- Study start
- Sep 1999
- Primary completion
- Feb 2000 (actual)
- First posted
- 11 Sep 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Study to obtain further information on the tolerability and efficacy of Atrovent® unit dose vial 500 µg in the treatment of Chronic Obstructive Airways Disease under conditions of daily practice
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Chronic Obstructive Airways Disease | – | Drug: Atrovent® |
Who may qualify
- Ages
- 30 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- Patients with chronic obstructive airways disease recruited at general practitioners, pneumologists, internists
Key inclusion criteria (2 listed)
- Primarily patients of both gender, older than 30 years, who suffer from chronic obstructive airways disease
- Only patients who had not been treated with Atrovent® within the last year were to be considered for inclusion
Key exclusion criteria (1 listed)
- Contraindication listed in the instructions for use/summary of product characteristics for Atrovent® unit dose vial 500 µg
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Atrovent® | Drug | Chronic Obstructive Airways Disease |
Primary outcome
Change in total severity of the clinical picture rated on a 4-point scale
Time frame: after 4 weeks
5 secondary outcomes
Assessment of efficacy by investigator on a 4-point scale
Time frame: after 4 weeks
Assessment of efficacy by patient on a 4-point scale
Time frame: after 4 weeks
Assessment of tolerability by investigator on a 4-point scale
Time frame: after 4 weeks
Assessment of tolerability by patient on a 4-point scale
Time frame: after 4 weeks
Number of patients with adverse drug reactions
Time frame: up to 4 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 11 Sep 2014.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
An observational study of Pulmonary Disease, Chronic Obstructive, run by Boehringer Ingelheim.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 11 Sep 2014. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in total severity of the clinical picture rated on a 4-point scale (time frame: after 4 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Sep 2014.