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Evaluation and Treatment of Pulmonary Vascular Disease in Moderate to Severe CF

12. juli 2019 oppdatert av: Jennifer Taylor-Cousar, National Jewish Health

Evaluation and Treatment of Pulmonary Vascular Disease in Moderate to Severe Cystic Fibrosis Lung Disease

This study evaluates the ability of the drug sildenafil to improved exercise capacity, cardiac performance during exercise, and quality of life in patients with moderate to severe CF lung disease. 3/4 of the subjects will receive sildenafil and 1/4 will receive placebo.

Studieoversikt

Status

Fullført

Forhold

Detaljert beskrivelse

Over time, patients with Cystic Fibrosis (CF) develop disabling lung disease that progresses to chronic respiratory failure, exercise intolerance with marked limitation of physical activity, and premature death. Despite substantial improvements in care, patients with CF often develop pulmonary vascular disease (PVD) that leads to pulmonary hypertension. Previous studies have clearly linked severe pulmonary hypertension and right heart failure with high mortality in CF. Early clinical manifestations of PVD prior to the development of cor pulmonale include shortness of breath and dyspnea with exertion, but the extent to which PVD contributes to the decline in exercise tolerance and quality of life in patients with CF is not known. Early evidence of PVD could be recognized in CF patients through standardized exercise testing and echocardiographic evaluation. Identifying those CF patients with PVD prior to the onset of right ventricular dysfunction may allow pharmacologic intervention to attenuate the progression of cardiovascular disease and improve quality of life. Clinical trials have demonstrated that treatment with the phosphodiesterase type 5 inhibitor, sildenafil, can decrease pulmonary vascular resistance and improve exercise tolerance in non-CF patients with pulmonary hypertension. Because experimental and clinical studies have implicated impaired NO-cGMP signaling in the pathophysiology of lung disease in CF, sildenafil may provide a novel pharmacological approach for treating PVD in patients with CF lung disease.

Studietype

Intervensjonell

Registrering (Faktiske)

14

Fase

  • Fase 2
  • Fase 1

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • Colorado
      • Denver, Colorado, Forente stater, 80206
        • National Jewish Health

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  1. Confirmed diagnosis of CF based on the following criteria: Positive sweat chloride ≥60mEq/liter (by pilocarpine iontophoresis) and/or Genotype with two identifiable mutations consistent with CF, and accompanied by one or more clinical features consistent with the CF phenotype
  2. Male or female patients ≥ 18 years of age
  3. FEV1 ≥ 20% predicted and ≤ 70% predicted (Hankinson)
  4. Clinically stable without evidence of acute upper or lower respiratory tract infection or current pulmonary exacerbation within the 14 days prior to the screening visit
  5. Ability to reproducibly perform spirometry (according to ATS criteria)
  6. Ability to understand and sign a written informed consent or assent and comply with the requirements of the study
  7. Willingness to maintain chronic CF medication schedule (e.g. alternating month inhaled antibiotics)

Exclusion Criteria:

  1. History of hypersensitivity to sildenafil
  2. Use of an investigational agent within the 4-week period prior to Visit 1 (Day 0)
  3. Breastfeeding, pregnant, or verbal expression of unwillingness to practice an acceptable birth control method (abstinence, hormonal or barrier methods, partner sterilization or intrauterine device) during participation in the study for women of child-bearing potential.
  4. History of significant hepatic disease (AST or ALT > 5 times the upper limit of normal at screening, documented biliary cirrhosis, or portal hypertension),
  5. History of significant cardiovascular disease (history of aortic stenosis, coronary artery disease, or life-threatening arrhythmia),
  6. History of severe neurological disease (e.g. history of stroke),
  7. History of severe hematologic disease (e.g. history of bleeding diathesis; current INR > 2.0
  8. History of severe ophthalmologic disease (e.g. history of retinal impairment or non-arteritic ischemic optic neuritis)
  9. History of severe renal impairment (creatinine >1.8 mg/dL.)
  10. Inability to swallow pills
  11. Previous organ transplantation
  12. Use of concomitant nitrates, α-blocker, or Ca channel blocker (currently or within one month of Visit 1)
  13. Use of concomitant medications known to be potent inhibitors of CYP3A4 [e.g. ketoconazole, itraconazole, ritonavir, clarithromycin, erythromycin, rifampin (currently or within one month of initiation of study drug)] NOTE: use of azithromycin is NOT a cause for exclusion
  14. History of sputum or throat swab culture yielding Burkholderia cepacia or Mycobacterium massiliense within 2 years of screening
  15. Weight less than 40 kg at Screening
  16. History of migraine headaches.
  17. Resting room air oxygen saturation <80% without supplemental oxygen
  18. Presence of a condition or abnormality that in the opinion of the investigator would compromise the safety of the subject or the quality of the data
  19. Start of CFTR modulator therapy less than 1 month prior to first dose of sildenafil or placebo
  20. Use of anticoagulants
  21. Frank pulmonary hypertension (RVSP >40 mmHg by ECHO)

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Firemannsrom

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: Sildenafil
Subjects will be randomized in a 3:1 (sildenafil:placebo) fashion. Subjects randomized to the treatment arm will receive sildenafil 20 mg p.o. t.i.d for 1 week followed by 40 mg p.o. t.i.d. for 11 weeks.
active sildenafil
Andre navn:
  • Revatio, Viagra
Placebo komparator: Placebo
Subjects randomized to the placebo arm will receive placebo p.o. t.i.d for 1 week followed by 2 placebo tablets p.o. t.i.d. for 11 weeks.
sugar pill that looks like sildenafil tablets

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
6 Minute Walk Distance
Tidsramme: Weeks 1, 13
Change in distance walked between week 1 and week 13 were compared. The difference between the two time points is reported.
Weeks 1, 13
Cardiopulmonary Exercise Test Work Rate
Tidsramme: Weeks 1 and 13
Work rate (the amount of energy being expended to cycle) was assessed at weeks 1 and 13. The change in maximum work measured during CPET between weeks 1 and 13 is reported.
Weeks 1 and 13

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Cystic Fibrosis Quality of Life-Revised Respiratory Domain Score
Tidsramme: Assessed at weeks 1 and 13
The CFQ-R Respiratory domain score (scale 0-100 with higher scores indicating better quality of life) was assessed at weeks 1 and 13. The change in the score between week 1 and week 13 is reported.
Assessed at weeks 1 and 13

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Etterforskere

  • Hovedetterforsker: Jennifer L Taylor-Cousar, MD, National Jewish Health

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart

1. desember 2015

Primær fullføring (Faktiske)

18. januar 2018

Studiet fullført (Faktiske)

29. januar 2018

Datoer for studieregistrering

Først innsendt

3. desember 2015

Først innsendt som oppfylte QC-kriteriene

7. desember 2015

Først lagt ut (Anslag)

10. desember 2015

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

24. juli 2019

Siste oppdatering sendt inn som oppfylte QC-kriteriene

12. juli 2019

Sist bekreftet

1. juli 2019

Mer informasjon

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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