Hôpital Tenon
Paris, France
NCT Number: NCT02460588
Acute exacerbation of idiopathic pulmonary fibrosis (AE-IPF) is a major event of IPF with an annual incidence between 5 and 10% and is responsible for the death of one third of IPF patients. When AE-IPF occurs, it is associated with poor survival with an overall mortality at 3 months upper of 50%. To date, no treatment has been proved to be effective in AE-IPF but the efficacy of cyclophosphamide (CYC) on survival has been suggested, mainly by retrospective series and needs to be confirmed. This confirmation is mandatory to improve prognosis of AE-IPF but also to avoid unsuspected deleterious effect as it as been shown with immunosuppressor in stable IPF.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Paris, France
Acute exacerbation of idiopathic pulmonary fibrosis (AE-IPF) is a major event of IPF with an annual incidence between 5 and 10% and is responsible for the death of one third of IPF patients. When AE-IPF occurs, it is associated with poor survival with an overall mortality at 3 months upper of 50%. To date, no treatment has been proved to be effective in AE-IPF but the efficacy of CYC on survival has been suggested, mainly by retrospective series and needs to be confirmed. This confirmation is mandatory to improve prognosis of AE-IPF but also to avoid unsuspected deleterious effect as it as been shown with immunosuppressor in stable IPF.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Population is IPF patients with an AE who meet the inclusion and exclusion criteria defined below.
Intravenous Cyclophosphamide (CYC), 600 mg/m² (adapted to age and renal function, maximal dose of 1.2 g) at Day 0, Day 15, M1, M2
Population is IPF patients with an AE who meet the inclusion and exclusion criteria defined below.
Other names: Control group
All patients will receive non experimental medication with high dose of corticosteroid.
Other names: Both groups
Time frame: 3 months
All cause of mortality at 3 months
Time frame: 6 months and 12 montns
Overall Survival at M6 and M12
Time frame: 6 months
Respiratory disease-specific mortality at M3 and M6
Time frame: 6 months
\\Worsening dyspnea (0-100-mm visual analogue (VAS) scale anchored with 0 ''no breathlessness'' and 10 or 100 ''worst imaginable breathlessness". Worsening is defined an absolute decrease of 10 mm)
Time frame: 6 months
Chest HRCT features at M3 and M6 compared to inclusion
Time frame: 3 months
PFTs results before AE-IPF
Time frame: 3 months
Time frame: 3 months
Time frame: 3 months
PaO2 at AE diagnosis
Time frame: 3 months
Chest HRCT features at AE diagnosis compared to HRCT before AE-IPF (if available)
Time frame: 3 months
Chest HRCT classification before AE-IPF (definite UIP, probable UIP, indeterminate), if available
Time frame: 3 months
Time frame: 6 months
Time frame: 6 months
Time frame: 6 months
Time frame: 6 months
Time frame: 6 months
Assistance Publique - Hôpitaux de Paris
Other
Cyclophosphamide Added to Corticosteroid in the Treatment of Acute Exacerbation of Idiopathic Pulmonary Fibrosis: a Placebo-controlled Randomized Trial
Acronym: EXAFIP
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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