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Methotrexate as a Steroid-sparing Agent in Idiopathic Retroperitoneal Fibrosis: a Randomised, Multicenter Trial (FIPREDEX)

Primary Purpose

Idiopathic Retroperitoneal Fibrosis, Perianeurysmal Retroperitoneal Fibrosis, Chronic Periaortitis

Status
Unknown status
Phase
Phase 3
Locations
Italy
Study Type
Interventional
Intervention
Methotrexate+Prednisone
Prednisone
Sponsored by
University of Parma
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Idiopathic Retroperitoneal Fibrosis focused on measuring Retroperitoneal fibrosis, Inflammatory aneurysms, Methotrexate, Prednisone, Aorta

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • New diagnosis of idiopathic retroperitoneal fibrosis or chronic periaortitis; written informed consent

Exclusion Criteria:

  • Secondary forms of retroperitoneal fibrosis (e.g. drugs, surgery, neoplasms, infections)
  • Previous medical therapy for retroperitoneal fibrosis
  • Renal failure with creatinine >2 mg/dl which proved not to be reversible after ureteral decompression
  • Hypersensitivity to the study drugs
  • Pregnancy
  • Active infections or malignant neoplasms

Sites / Locations

  • Nephrology Unit, University Hospital of ParmaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Prednisone

Methotrexate+Prednisone

Arm Description

Outcomes

Primary Outcome Measures

Remission rate by the end of treatment

Secondary Outcome Measures

Reduction in size of the retroperitoneal mass on CT/MRI scans
Rate of post-treatment relapses
Treatment-related toxicity

Full Information

First Posted
November 12, 2010
Last Updated
November 12, 2010
Sponsor
University of Parma
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1. Study Identification

Unique Protocol Identification Number
NCT01240850
Brief Title
Methotrexate as a Steroid-sparing Agent in Idiopathic Retroperitoneal Fibrosis: a Randomised, Multicenter Trial
Acronym
FIPREDEX
Official Title
Medical Therapy in Idiopathic Retroperitoneal Fibrosis: a Multicenter, Randomized, Controlled Trial of Prednisone vs Low-dose Prednisone Plus Methotrexate
Study Type
Interventional

2. Study Status

Record Verification Date
November 2010
Overall Recruitment Status
Unknown status
Study Start Date
May 2007 (undefined)
Primary Completion Date
May 2012 (Anticipated)
Study Completion Date
December 2013 (Anticipated)

3. Sponsor/Collaborators

Name of the Sponsor
University of Parma

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Chronic periaortitis is a clinico-pathological entity encompassing idiopathic retroperitoneal fibrosis and perianeurysmal retroperitoneal fibrosis. The treatment of this disease is generally based on the use of glucocorticoids, which are often effective. However, prolonged steroid treatments are usually needed to achieve a sustained remission; additionally, patients frequently develop disease relapses following treatment discontinuation, therefore they may be exposed to high cumulative doses of glucocorticoids. Preliminary data reported in the literature show that methotrexate may be effective in combination with prednisone for retroperitoneal fibrosis. In addition, methotrexate is often used as a steroid-sparing agent in different inflammatory diseases. The aim of this study is to evaluate whether a treatment with low-dose prednisone plus methotrexate is non-inferior to conventional dose-prednisone in achieving remission in retroperitoneal fibrosis patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Idiopathic Retroperitoneal Fibrosis, Perianeurysmal Retroperitoneal Fibrosis, Chronic Periaortitis
Keywords
Retroperitoneal fibrosis, Inflammatory aneurysms, Methotrexate, Prednisone, Aorta

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Prednisone
Arm Type
Active Comparator
Arm Title
Methotrexate+Prednisone
Arm Type
Experimental
Intervention Type
Drug
Intervention Name(s)
Methotrexate+Prednisone
Intervention Description
Methotrexate will be added at a dose of 0.3 mg/kg/week (maximum dose, 20 mg/week, orally) to a reduced-dose prednisone regimen
Intervention Type
Drug
Intervention Name(s)
Prednisone
Primary Outcome Measure Information:
Title
Remission rate by the end of treatment
Secondary Outcome Measure Information:
Title
Reduction in size of the retroperitoneal mass on CT/MRI scans
Title
Rate of post-treatment relapses
Title
Treatment-related toxicity

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: New diagnosis of idiopathic retroperitoneal fibrosis or chronic periaortitis; written informed consent Exclusion Criteria: Secondary forms of retroperitoneal fibrosis (e.g. drugs, surgery, neoplasms, infections) Previous medical therapy for retroperitoneal fibrosis Renal failure with creatinine >2 mg/dl which proved not to be reversible after ureteral decompression Hypersensitivity to the study drugs Pregnancy Active infections or malignant neoplasms
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Carlo Buzio, MD
Phone
+39 0521 702345
Email
carlo.buzio@unipr.it
First Name & Middle Initial & Last Name or Official Title & Degree
Augusto Vaglio, MD, PhD
Phone
+39 0521 702345
Email
augusto.vaglio@virgilio.it
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Augusto Vaglio, MD, PhD
Organizational Affiliation
Parma University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Nephrology Unit, University Hospital of Parma
City
Parma
ZIP/Postal Code
43126
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Augusto Vaglio, MD PhD
Phone
+39 0521 702345
Email
augusto.vaglio@virgilio.it
First Name & Middle Initial & Last Name & Degree
Augusto Vaglio, MD PhD

12. IPD Sharing Statement

Citations:
PubMed Identifier
17472843
Citation
van Bommel EF, Siemes C, Hak LE, van der Veer SJ, Hendriksz TR. Long-term renal and patient outcome in idiopathic retroperitoneal fibrosis treated with prednisone. Am J Kidney Dis. 2007 May;49(5):615-25. doi: 10.1053/j.ajkd.2007.02.268.
Results Reference
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PubMed Identifier
18037118
Citation
Vaglio A, Palmisano A, Corradi D, Salvarani C, Buzio C. Retroperitoneal fibrosis: evolving concepts. Rheum Dis Clin North Am. 2007 Nov;33(4):803-17, vi-vii. doi: 10.1016/j.rdc.2007.07.013.
Results Reference
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PubMed Identifier
16427494
Citation
Vaglio A, Salvarani C, Buzio C. Retroperitoneal fibrosis. Lancet. 2006 Jan 21;367(9506):241-51. doi: 10.1016/S0140-6736(06)68035-5.
Results Reference
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PubMed Identifier
15897305
Citation
Warnatz K, Keskin AG, Uhl M, Scholz C, Katzenwadel A, Vaith P, Peter HH, Walker UA. Immunosuppressive treatment of chronic periaortitis: a retrospective study of 20 patients with chronic periaortitis and a review of the literature. Ann Rheum Dis. 2005 Jun;64(6):828-33. doi: 10.1136/ard.2004.029793.
Results Reference
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Learn more about this trial

Methotrexate as a Steroid-sparing Agent in Idiopathic Retroperitoneal Fibrosis: a Randomised, Multicenter Trial

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