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| Sponsor: | University Medical Centre Groningen |
|---|---|
| Information provided by: | University Medical Centre Groningen |
| ClinicalTrials.gov Identifier: | NCT00127764 |
Purpose
By this study, the investigators want to test if the value of adjuvant pulse glucocorticoid therapy for pemphigus can be determined by comparing an experimental arm (dexamethasone pulse therapy, prednisolone, and azathioprine) with a control arm (placebo pulse therapy, prednisolone, and azathioprine). The investigators will determine the rate of complete remission with dexamethasone pulse therapy; the time needed for complete remission; and the duration of remission, and compare these data with those of the placebo arm.
| Condition | Intervention | Phase |
|---|---|---|
|
Pemphigus |
Drug: dexamethasone (50mg 1dd6, 3 consecutive days/month) |
Phase II Phase III |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study |
| Official Title: | European Randomised Placebo-Controlled Trial of Adjuvant Oral Glucocorticoid Pulse Therapy in Pemphigus (Pempuls Trial) |
| Estimated Enrollment: | 60 |
| Study Start Date: | January 2001 |
| Estimated Study Completion Date: | April 2005 |
Pemphigus is a severe chronic dermatological disease which appears to be incurable. Oral glucocorticoid now forms the cornerstone of treatment. From previous uncontrolled studies it has been suggested, that the use of high dose intravenous glucocorticoid pulse therapy may lead to complete remission without further therapy. Prospective placebo-controlled studies of adjuvant pulse therapy for pemphigus are lacking. This prospective, multi-centre, randomised, double-blind, placebo-controlled trial assesses the efficacy and steroid-sparing effect of oral high-dose glucocorticoid pulse therapy as adjuvant added to the standard combination therapy of prednisone and azathioprine in the treatment of pemphigus vulgaris, in terms of complete remission rate (primary endpoint), initial control, disease control, and adverse events. In the experimental arm glucocorticoid pulse therapy is given, comprising monthly pulses with 300mg oral dexamethasone on three consecutive days. In addition the patients receive daily prednisone and azathioprine treatment, the latter dose adjusted to the thiopurine-methyltransferase level. In the control arm the glucocorticoid pulse therapy is replaced double blindly by monthly oral placebo capsules on three consecutive days. in addition the patients receive the same daily combination schedule with prednisone and azathioprine as in the experimental arm. This study design requires 30 patients in each arm, with one year follow-up. Only new patients with pemphigus vulgaris and/or pemphigus oris are included.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Netherlands | |
| Department of Dermatology, University Medical Center Groningen | |
| Groningen, Netherlands, 9713 GZ | |
| Principal Investigator: | Marcel F Jonkman, MD, PhD | Department of Dermatology, University Medical Center Groningen |
More Information
| Study ID Numbers: | 754309 |
| Study First Received: | August 4, 2005 |
| Last Updated: | August 29, 2007 |
| ClinicalTrials.gov Identifier: | NCT00127764 History of Changes |
| Health Authority: | Netherlands: The Central Committee on Research Involving Human Subjects (CCMO) |
|
pemphigus dexamethasone glucocorticoids pulse |
therapy randomised placebo-controlled |
|
Anti-Inflammatory Agents Dexamethasone Autoimmune Diseases Antineoplastic Agents, Hormonal Skin Diseases, Vesiculobullous Skin Diseases Immune System Diseases Antineoplastic Agents Physiological Effects of Drugs Hormones, Hormone Substitutes, and Hormone Antagonists Gastrointestinal Agents |
Antiemetics Hormones Glucocorticoids Pharmacologic Actions Pemphigus Autonomic Agents Therapeutic Uses Peripheral Nervous System Agents Central Nervous System Agents Dexamethasone acetate |