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Prednisone Versus Tamoxifen in Idiopathic Retroperitoneal Fibrosis
This study is ongoing, but not recruiting participants.
Sponsored by: University of Parma
Information provided by: University of Parma
ClinicalTrials.gov Identifier: NCT00440349
  Purpose

Idiopathic retroperitoneal fibrosis (IRF) is a rare disease characterised by the presence of a retroperitoneal periaortic fibro-inflammatory tissue which may entrap the ureters and cause renal failure. The treatment of IRF is not well established. Corticosteroids are frequently used, but the anti-estrogen agent tamoxifen has also been reported to be effective in a number of reports. However, no randomised trials have been published so far. The aim of the present study is to compare the efficacy of prednisone and tamoxifen in the treatment of IRF.


Condition Intervention Phase
Retroperitoneal Fibrosis
Drug: Tamoxifen
Drug: Prednisone
Phase II

Drug Information available for: Prednisone Tamoxifen Tamoxifen citrate Corticosteroids
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title: A Randomised Trial of Prednisone and Tamoxifen in Patients With Idiopathic Retroperitoneal Fibrosis

Further study details as provided by University of Parma:

Primary Outcome Measures:
  • Difference in recurrence rate at the end of treatment

Secondary Outcome Measures:
  • Difference in reduction in size of IRF (as assessed by CT/MRI)
  • Difference in renal function

Estimated Enrollment: 38
Study Start Date: October 2000
Estimated Study Completion Date: April 2007
Detailed Description:

Idiopathic retroperitoneal fibrosis (IRF) is a rare condition hallmarked by the presence of a retroperitoneal mass consisting of chronic inflammatory infiltrate and abundant fibrous tissue. IRF usually presents as a systemic inflammatory disease, with constitutional symptoms (e.g. fatigue, weight loss) and high acute-phase reactants; in addition, IRF patients often complain of abdominal or lumbar pain and, if ureteral involvement is present, they may also show oliguria and symptoms related to uremia.

Ureteral obstructive disease is usually managed by placement of ureteral indwelling stents, nephrostomy tubes or, in the more severe cases, surgical ureterolysis. These approaches are usually followed by medical treatment.

The medical treatment of IRF is largely empirical: corticosteroids are routinely used, but a number of reports have shown that tamoxifen may also be effective. However, no prospective controlled trials have been conducted in patients with this condition. In this study, we compare the efficacy of prednisone and tamoxifen in IRF patients.

Patients who received a diagnosis of IRF will be enrolled, while patients with secondary forms of retroperitoneal fibrosis (e.g. drugs, infections, radiotherapy) will be excluded. When present, ureteral obstruction will be managed by ureteral stents/nephrostomy/ureterolysis. All patients will then receive oral prednisone (1 mg/kg/day) for one month, at the end of which they will be randomized to receive either tamoxifen (0.5 mg/kg/day at fixed dose for 8 months) or prednisone (0.5 mg/kg/day for the first month, 0.25 mg/kg/day for the second and third months, and then tapered off during the ensuing 5 months). A CT/MRI study will be performed before the start of treatment, four months after randomization and at the end of treatment. All patients will be followed up for at least 18 months after the end of treatment.

Disease remission will be defined on the basis of clinical symptoms related to IRF (e.g. pain, constitutional symptoms), levels of acute-phase reactants (erythrocyte sedimentation rate, C-reactive protein), and ureteral obstruction (as assessed by sonography or CT/MRI scan).

  Eligibility

Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Diagnosis of idiopathic or perianeurismal retroperitoneal fibrosis

Exclusion Criteria:

  • Previously treated patients; retroperitoneal fibrosis secondary to drugs(e.g. methysergide, methyldopa, pergolide, ergot alkaloids), infections (e.g. tuberculosis), cancer (e.g. lymphoma, sarcoma), radiotherapy, trauma, major surgery, systemic connective tissue or vasculitis disease (e.g. SLE, panarteritis nodosa); pregnancy; active infections or tumours; known hypersensitivity to prednisone or tamoxifen; uncontrolled diabetes.
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00440349

Locations
Italy
Department of Clinical Medicine Nephrology and Health Science, Parma University Hospital
Parma, Italy, 43100
Sponsors and Collaborators
University of Parma
Investigators
Principal Investigator: Carlo Buzio, MD University of Parma
  More Information

Publications:
Study ID Numbers: FR09
Study First Received: February 23, 2007
Last Updated: February 23, 2007
ClinicalTrials.gov Identifier: NCT00440349  
Health Authority: Italy: Ethics Committee

Keywords provided by University of Parma:
Retroperitoneal fibrosis
Tamoxifen
Corticosteroids
Obstructive uropathy
Periaortic fibrosis
Chronic periaortitis

Study placed in the following topic categories:
Retroperitoneal fibrosis
Prednisone
Urologic Diseases
Fibrosis
Retroperitoneal Fibrosis
Tamoxifen

Additional relevant MeSH terms:
Anti-Inflammatory Agents
Estrogen Antagonists
Antineoplastic Agents, Hormonal
Antineoplastic Agents
Hormone Antagonists
Physiological Effects of Drugs
Hormones, Hormone Substitutes, and Hormone Antagonists
Bone Density Conservation Agents
Selective Estrogen Receptor Modulators
Glucocorticoids
Hormones
Pharmacologic Actions
Estrogen Receptor Modulators
Pathologic Processes
Therapeutic Uses

ClinicalTrials.gov processed this record on January 14, 2009