- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving 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)
Studieoversikt
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
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Alabama
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Birmingham, Alabama, Forente stater, 35294
- UAB Lung Health Center
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Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
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
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Behandling
- Tildeling: Randomisert
- Intervensjonsmodell: Parallell tildeling
- Masking: Trippel
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
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Placebo komparator: 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
Andre navn:
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Induced Sputum Proline-glycine-proline (PGP) Levels at Baseline
Tidsramme: baseline
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baseline
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Mean Induced Sputum Proline-glycine-proline (PGP) Levels at 1 Month After Randomization.
Tidsramme: 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
Tidsramme: 3 months after baseline
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3 months after baseline
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Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Induced Sputum Neutrophil Count
Tidsramme: 1 month
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1 month
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Induced Sputum Neutrophil Count
Tidsramme: baseline
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baseline
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Induced Sputum Neutrophil Count
Tidsramme: 3 months after baseline
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3 months after baseline
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Samarbeidspartnere og etterforskere
Etterforskere
- Hovedetterforsker: James E Blalock, PhD, University of Alabama at Birmingham
Publikasjoner og nyttige lenker
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- DAL-MD-01
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