- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT01572948
A Placebo-controlled Trial of Daliresp on Chronic Obstructive Pulmonary Disease (COPD)
A Placebo-controlled Trial of Roflumilast (Daliresp) on Markers of Inflammation in Chronic Obstructive Pulmonary Disease (COPD)
Studieöversikt
Studietyp
Inskrivning (Faktisk)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
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Alabama
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Birmingham, Alabama, Förenta staterna, 35294
- UAB Lung Health Center
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Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- Male and female subjects, > 40 years of age
Clinical diagnosis of moderate to severe COPD as defined by the GOLD criteria:
Post-bronchodilator FEV1/FVC < 70% Post-bronchodilator FEV1 < 70% predicted
- Cigarette consumption of 10 pack-years or more. Patients may be active smokers.
- The presence of chronic cough and sputum production
- Willingness to make return visits and telephone availability for the study duration
Exclusion Criteria:
- A diagnosis of asthma as established by the study investigator on the basis of the recent American Thoracic Society/European Respiratory Society guidelines
- Clinically significant bronchiectasis
- Oxygen use >12 hours/day
- Known sensitivity to roflumilast
- Use of other methylxanthines within 1 month (theophylline)
- Changes to current maintenance COPD therapy within one month
- Pregnancy
- An acute illness requiring antibiotics and/or corticosteroids within the month prior to enrolment.
Immunosuppression
- HIV
- Solid organ transplant
- Active malignancy
- Systemic corticosteroid use ≥ prednisone 20mg / day
- Other immunosuppressants
- Terminal illness defined as anticipated survival <12 months
Severe comorbidities including uncontrolled angina, congestive heart failure, end-stage renal disease, liver failure, or other conditions that would preclude the patient from safely completing the required tests or the study.
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Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Trippel
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
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Placebo-jämförare: Placebo
The placebo (Forest Laboratories, Inc) is manufactured as an odorless and otherwise equivalent tablet to the roflumilast tablet, but contains no active ingredient.
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The placebo (Forest Laboratories, Inc) is manufactured as an odorless and otherwise equivalent tablet to the roflumilast tablet, but contains no active ingredient
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Aktiv komparator: Daliresp
The study drug (roflumilast, Daliresp™, Forest Laboratories, Inc.) is a targeted inhibitor of phosphodiesterase 4 and is given once daily via oral route.
There is proven anti-inflammatory and anti-oxidant potential in both animal and human models
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The study drug (roflumilast, Daliresp™, Forest Laboratories, Inc.) is a targeted inhibitor of phosphodiesterase 4 and is given once daily via oral route.
There is proven anti-inflammatory and anti-oxidant potential in both animal and human models
Andra namn:
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Tidsram |
|---|---|
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Induced Sputum Proline-glycine-proline (PGP) Levels at Baseline
Tidsram: baseline
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baseline
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Mean Induced Sputum Proline-glycine-proline (PGP) Levels at 1 Month After Randomization.
Tidsram: 1 month after baseline
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1 month after baseline
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Mean Induced Sputum Proline-glycine-proline (PGP) Levels at 3 Months After Randomization
Tidsram: 3 months after baseline
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3 months after baseline
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Sekundära resultatmått
Resultatmått |
Tidsram |
|---|---|
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Induced Sputum Neutrophil Count
Tidsram: 1 month
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1 month
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Induced Sputum Neutrophil Count
Tidsram: baseline
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baseline
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Induced Sputum Neutrophil Count
Tidsram: 3 months after baseline
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3 months after baseline
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Samarbetspartners och utredare
Utredare
- Huvudutredare: James E Blalock, PhD, University of Alabama at Birmingham
Publikationer och användbara länkar
Studieavstämningsdatum
Studera stora datum
Studiestart
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Uppskatta)
Uppdateringar av studier
Senaste uppdatering publicerad (Uppskatta)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
Andra studie-ID-nummer
- DAL-MD-01
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