Cardiology Prevention in Systemic Lupus Erythematosus (SLE)
Primary Purpose
Systemic Lupus Erythematosus
Status
Withdrawn
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Preventive Cardiology
Usual Care
Sponsored by
About this trial
This is an interventional prevention trial for Systemic Lupus Erythematosus focused on measuring SLE, lupus, cardiovascular, IMT, Systemic Lupus Erythematosus
Eligibility Criteria
Inclusion Criteria:
- Definitive diagnosis of SLE
- >18 years of age
- Followed by rheumatologists (not the investigator, Dr. Elliott) at the Lupus Center of Excellence
- Informed consent signed
- Effective form of birth control
Exclusion Criteria:
- Prior cardiovascular disease history (MI, coronary angioplasty, coronary artery bypass graft, abnormal coronary angiography, abnormal nuclear or treadmill stress test)
- Prior evaluation by preventive cardiology
- Active cardiac issues
- Pregnancy, breastfeeding, or anticipating pregnancy in the next 2 years
Sites / Locations
- Lupus Center of Excellence, Magee Womens Hospital, 300 Halket St, Suite 1750
- Clinical and Translational Research Center (CTRC), Montefiore Hospital, 6NE, 200 Lothrop St.
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
1
2
Arm Description
Participants randomized to this arm (n=15) will be followed by Preventive Cardiology and will have appropriate goal oriented interventions on their risk factor levels for 2 years.
Participants randomized to this arm (n=15) will receive usual care. The PI will send a letter of all testing results to their primary care physician. No standard care will be withheld.
Outcomes
Primary Outcome Measures
The efficacy of a preventive cardiology program compared to usual care in slowing the progression of carotid IMT and plaque
The effect of a preventive cardiology program versus usual care at achieving CV risk factor target goals.
Secondary Outcome Measures
Full Information
NCT ID
NCT00610805
First Posted
January 24, 2008
Last Updated
January 14, 2016
Sponsor
University of Pittsburgh
Collaborators
Arthritis Foundation, National Institutes of Health (NIH)
1. Study Identification
Unique Protocol Identification Number
NCT00610805
Brief Title
Cardiology Prevention in Systemic Lupus Erythematosus (SLE)
Official Title
Cardiology Prevention Trial in Systemic Lupus Erythematosus
Study Type
Interventional
2. Study Status
Record Verification Date
January 2016
Overall Recruitment Status
Withdrawn
Study Start Date
November 2009 (undefined)
Primary Completion Date
November 2009 (Actual)
Study Completion Date
November 2009 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
University of Pittsburgh
Collaborators
Arthritis Foundation, National Institutes of Health (NIH)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
We propose a feasibility study of aggressive CV risk factor management directed by preventive cardiology compared to usual care. We will determine: 1) the efficacy of a preventive cardiology program compared to usual care in slowing the progression of carotid IMT and plaque, and 2) the effect of a preventive cardiology program versus usual care at achieving CV risk factor target goals.
We hypothesize Lupus patients randomized to the preventive cardiology program will have less cardiovascular progression over two years than those lupus patients who are given standard care for cardiovascular risk, defined by carotid intima-media thickness and plaque.
Detailed Description
We will recruit 30 eligible patients from the Lupus Center of Excellence outpatient clinic. Patients will either be randomized into a preventive cardiology program for aggressive treatment, or randomized to usual care (1:1 ratio) in a single-blinded, randomized trial of 24 months duration. In this feasibility trial we hope to identify and refine any limitations in anticipation of designing a larger, randomized intervention study.
For both arms of the study, at baseline, 6 month, 12 month, 18 month, and 24 month visits (5 visits in total) all patients will be seen by Dr. Elliott, Principal Investigator. Visits will include an interview, fasting laboratory tests completion of questionnaires regarding demographics, socioeconomic status, health status, and risk factors (traditional, inflammatory, and lupus-specific). Dr. Elliott will perform the physical examinations on all patients and complete the lupus-specific disease activity and damage questionnaires. At the Baseline visit, 12-month visit, and 24 24-month visits, all patients will have a carotid ultrasound.
Cohort 1: Preventive Cardiology Program arm: Above and beyond the standard care, which is listed below, the patients in this arm will be aggressively treated by the cardiologist. As deemed prudent, the following may be prescribed: antihypertensives, lipid reducing agents, anti-platelets, further cardiac testing, and behavioral modifications. No standard care treatment will be withheld.
Cohort 2: Standard Care arm: The PI will send a letter of all testing results to their designated PCP. No standard care treatment will be withheld.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Systemic Lupus Erythematosus
Keywords
SLE, lupus, cardiovascular, IMT, Systemic Lupus Erythematosus
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Investigator
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Participants randomized to this arm (n=15) will be followed by Preventive Cardiology and will have appropriate goal oriented interventions on their risk factor levels for 2 years.
Arm Title
2
Arm Type
Other
Arm Description
Participants randomized to this arm (n=15) will receive usual care. The PI will send a letter of all testing results to their primary care physician. No standard care will be withheld.
Intervention Type
Other
Intervention Name(s)
Preventive Cardiology
Intervention Description
Patients will receive those interventions recommended by the Preventive Cardiologist. This may include: exercise, electrocardiogram, specialized blood testing, blood pressure monitoring, nutrition counseling, smoking cessation counseling, and pharmacotherapy for hypercholesterolemia, hypertension, and blood sugar abnormalities.
Intervention Type
Other
Intervention Name(s)
Usual Care
Intervention Description
Participants will receive usual care per their primary care physician.
Primary Outcome Measure Information:
Title
The efficacy of a preventive cardiology program compared to usual care in slowing the progression of carotid IMT and plaque
Time Frame
2 years
Title
The effect of a preventive cardiology program versus usual care at achieving CV risk factor target goals.
Time Frame
2 years
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Definitive diagnosis of SLE
>18 years of age
Followed by rheumatologists (not the investigator, Dr. Elliott) at the Lupus Center of Excellence
Informed consent signed
Effective form of birth control
Exclusion Criteria:
Prior cardiovascular disease history (MI, coronary angioplasty, coronary artery bypass graft, abnormal coronary angiography, abnormal nuclear or treadmill stress test)
Prior evaluation by preventive cardiology
Active cardiac issues
Pregnancy, breastfeeding, or anticipating pregnancy in the next 2 years
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jennifer R Elliott, MD
Organizational Affiliation
University of Pittsburgh
Official's Role
Principal Investigator
Facility Information:
Facility Name
Lupus Center of Excellence, Magee Womens Hospital, 300 Halket St, Suite 1750
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15213
Country
United States
Facility Name
Clinical and Translational Research Center (CTRC), Montefiore Hospital, 6NE, 200 Lothrop St.
City
Pittsburgh
State/Province
Pennsylvania
ZIP/Postal Code
15261
Country
United States
12. IPD Sharing Statement
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Cardiology Prevention in Systemic Lupus Erythematosus (SLE)
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