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UnknownNCT00399399

CHUSPAN SCS BP Treatment of Churg-Strauss Syndrome Without Poor-Prognosis Factors

CHUSPAN SCS BP Treatment of Churg-Strauss Syndrome Without Poor-Prognosis Factors: a Prospective Randomized Study in 72 Patients.

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
72 (planned)
Sponsor
Hospices Civils de Lyon · Academic / Other
Sex
All
Age
15 Years – 90 Years
Healthy volunteers
Not accepted

Summary

To assess the efficacy of systemic corticosteroids alone as first-line treatment of Churg-Strauss syndrome without poor-prognosis factors as defined by the five-factor score (FFS=0), and to compare the efficacy and safety of azathioprine vs pulse cyclophosphamide as adjunctive immunosuppressive therapy to treat failure or relapse

Detailed description

All patients initially treated with systemic corticosteroids alone: optional IV methylprednisolone pulse (15 mg/kg) at treatment start followed by oral prednisone (1 mg/kg/day) according to a tapering schedule. Treating physicians allowed to treat minor relapses with corticosteroids without referring the patient for randomization, as long as the prednisone dose did not exceed 0.5 mg/kg for 1 month. Patients in whom prednisone doses could not be tapered below 20 mg, those who failed to enter remission and those who relapsed were randomized to receive either 6 months of oral azathioprine (2mg/kg/day) or 6 cyclophosphamide pulses (0.6g/m2 D1, D15, D30 then every month)

Conditions

Interventions

TypeNameDescription
DRUGazathioprine
DRUGcyclophosphamide

Timeline

Start date
1996-07-01
First posted
2006-11-14
Last updated
2006-11-14

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT00399399. Inclusion in this directory is not an endorsement.

CHUSPAN SCS BP Treatment of Churg-Strauss Syndrome Without Poor-Prognosis Factors (NCT00399399) · Clinical Trials Directory