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Atorvastatin to Prevent Avascular Necrosis of Bone in Steroid Treated Exacerbated Systemic Lupus Erythematosus

Primary Purpose

Avascular Necrosis

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Atorvastatin
MRI, Venipuncture
Placebo
Sponsored by
NYU Langone Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Avascular Necrosis focused on measuring Avascular Necrosis, Lipitor, SLE

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • All individuals must fulfill 4 of the revised criteria of the American College of Rheumatology for SLE
  • Patient started on corticosteroids at a dose of at least .5mg/kg for an interval greater than two weeks
  • To be able to come for all follow-up visits for nine months
  • No contraindications to undergoing MRI
  • Age 18-75 years

Exclusion Criteria:

  • Evidence of liver disease, not secondary to active lupus, or liver enzyme greater than 2x normal
  • Elevated CPK at baseline
  • Pregnancy or Lactating
  • Allergy to a statin
  • Current or recent use of a statin within 3 months

Sites / Locations

  • The New York University Hospital For Joint Diseases

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Atorvastatin

Placebo

Arm Description

Atorvastatin 40mg

Tablets identical to atorvastatin 40mg

Outcomes

Primary Outcome Measures

Number of Participants With AVN After 9 Months

Secondary Outcome Measures

Number of Participants With AVN After 4 Months
To Determine if Atorvastatin is Effective in Lowering Serum Lipid Levels Chol, TG, HDL, & LDL in SLE Patients
To Determine if Atorvastatin Has an Anti-inflammatory Effect in Active SLE That Reduces Biological Markers of the Inflammatory Process (ESR, Hs-CRP) and Reduces Disease Activity Assessed by Serology (C3, C4, Anti-dsDNA) or Clinical Instrument (SLEDAI)

Full Information

First Posted
December 18, 2006
Last Updated
October 23, 2018
Sponsor
NYU Langone Health
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1. Study Identification

Unique Protocol Identification Number
NCT00412841
Brief Title
Atorvastatin to Prevent Avascular Necrosis of Bone in Steroid Treated Exacerbated Systemic Lupus Erythematosus
Official Title
AVN Prevention With Lipitor in Lupus Erythematosus APLLE Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2018
Overall Recruitment Status
Terminated
Study Start Date
November 2002 (undefined)
Primary Completion Date
January 2008 (Actual)
Study Completion Date
January 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
NYU Langone Health

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study uses the cholesterol lowering drug atorvastatin, also known as lipitor, to show reduction of avascular necrosis in steroid treated lupus patients. Avascular necrosis is a disease resulting from the loss of blood supply to the bones which can cause the bone to collapse. The collapse of bone may require a surgical replacement of the joint and can be disabling for life. Avascular necrosis is presently not preventable but research has shown that lipid lowering drugs such as lipitor can reduce or prevent avascular necrosis in animals. We therefore hypothesize that lipitor will reduce the incidence of avascular necrosis in lupus patients taking high dose steroids.
Detailed Description
If you have started on prednisone 30mg or greater and expect to be on it for greater than two weeks you may be a candidate for the study. Also, you would need to be enrolled in the study within three days of starting prednisone. If you are eligible you will receive lipitor 40mg per day or pills which look exactly like lipitor but do not contain any medication (called placebo). During the time of the study, you will not know if you are taking lipitor or the placebo. The period of time that you will receive lipitor or placebo is 9 months and you must be willing to return for 5 follow up visits during this time which include blood tests, physical exams and 3 MRI studies of the hips, knees and ankles.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Avascular Necrosis
Keywords
Avascular Necrosis, Lipitor, SLE

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
43 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Atorvastatin
Arm Type
Experimental
Arm Description
Atorvastatin 40mg
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Tablets identical to atorvastatin 40mg
Intervention Type
Drug
Intervention Name(s)
Atorvastatin
Other Intervention Name(s)
Atorvasatatin 40mg vs Placebo
Intervention Description
Atorvastatin 40mg vs placebo 40mg daily
Intervention Type
Procedure
Intervention Name(s)
MRI, Venipuncture
Other Intervention Name(s)
MRI at baseline, 4 months and 9 months
Intervention Description
MRIs done baseline, four and nine months
Intervention Type
Drug
Intervention Name(s)
Placebo
Intervention Description
Tablets identical to atorvastatin 40mg
Primary Outcome Measure Information:
Title
Number of Participants With AVN After 9 Months
Time Frame
9 months
Secondary Outcome Measure Information:
Title
Number of Participants With AVN After 4 Months
Time Frame
4 months
Title
To Determine if Atorvastatin is Effective in Lowering Serum Lipid Levels Chol, TG, HDL, & LDL in SLE Patients
Time Frame
6 years
Title
To Determine if Atorvastatin Has an Anti-inflammatory Effect in Active SLE That Reduces Biological Markers of the Inflammatory Process (ESR, Hs-CRP) and Reduces Disease Activity Assessed by Serology (C3, C4, Anti-dsDNA) or Clinical Instrument (SLEDAI)
Time Frame
6 years

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All individuals must fulfill 4 of the revised criteria of the American College of Rheumatology for SLE Patient started on corticosteroids at a dose of at least .5mg/kg for an interval greater than two weeks To be able to come for all follow-up visits for nine months No contraindications to undergoing MRI Age 18-75 years Exclusion Criteria: Evidence of liver disease, not secondary to active lupus, or liver enzyme greater than 2x normal Elevated CPK at baseline Pregnancy or Lactating Allergy to a statin Current or recent use of a statin within 3 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Howard M Belmont, M.D.
Organizational Affiliation
The New York University Hospital for Joint Diseases
Official's Role
Principal Investigator
Facility Information:
Facility Name
The New York University Hospital For Joint Diseases
City
New York
State/Province
New York
ZIP/Postal Code
10003
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
16302686
Citation
Belmont HM, Lydon E. Avascular necrosis prevention with lipitor in lupus erythematosus. Lupus. 2005;14(10):869-70. doi: 10.1191/0961203305lu2189xx. No abstract available.
Results Reference
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Atorvastatin to Prevent Avascular Necrosis of Bone in Steroid Treated Exacerbated Systemic Lupus Erythematosus

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