Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| DRUG | azathioprine | |
| DRUG | cyclophosphamide |
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.