Early Vascular Wall Changes by Magnetic Resonance Imaging (MRI) in Metabolic Syndrome Versus Metabolically Normal Pre-Menopausal Women: A Pilot Study

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
University of Washington
ClinicalTrials.gov Identifier:
NCT01068535
First received: February 11, 2010
Last updated: September 12, 2012
Last verified: September 2012

February 11, 2010
September 12, 2012
May 2009
July 2012   (final data collection date for primary outcome measure)
ktrans of the carotid artery wall [ Time Frame: baseline ] [ Designated as safety issue: No ]
Ktrans is a transfer constant that is a measure of vascular permeability.
Not Provided
Complete list of historical versions of study NCT01068535 on ClinicalTrials.gov Archive Site
carotid artery intima-media thickness as measured by MRI [ Time Frame: baseline ] [ Designated as safety issue: No ]
Carotid intima-media thickness is a measure of the actual thickness of the intima and media layers of the carotid artery wall.
Not Provided
Not Provided
Not Provided
 
Early Vascular Wall Changes by Magnetic Resonance Imaging (MRI) in Metabolic Syndrome Versus Metabolically Normal Pre-Menopausal Women: A Pilot Study
Early Vascular Wall Changes by MRI in Metabolic Syndrome vs. Metabolically Normal Pre-Menopausal Women: A Pilot Study

The purpose of this study is to compare the vascular permeability of blood vessel walls (of the carotid artery) in pre-menopausal women who have metabolic syndrome (syndrome of having at least 3/5 following features- increased abdominal fat, low good cholesterol (HDL-C), elevated fasting blood fats (triglycerides), elevated blood pressure, an elevated fasting glucose) versus those women who are normal weight and with normal cholesterol, blood fats, blood pressure, and blood sugar. We are using a novel technology to measure vascular permeability known as dynamic contrast enhancement magnetic resonance imaging (DCE-MRI). The primary variable is ktrans ratio which is a mathematically derived quantity obtained from DCE-MRI. We are trying to identify novel markers of early atherosclerosis in young women.

This study involves a phone screen & 2 study visits:

  • Screening visit, which includes a quick finger stick cholesterol, glucose, triglycerides test (cholestech) to determine qualification, waist measurement, weight. Results are provided regardless of qualification. If the volunteer qualifies, a full blood draw (approximately 45cc or 3 Tablespoons) will occur. A snack is provided once blood is drawn. Additional study visit procedures include a medical history questionnaire including menstrual history, height & weight measurement, vital signs, and waist & hip measurements. This study lasts up to 90 minutes.
  • MRI visit (to occur within a week of screening visit) occurs once serum pregnancy & creatinine results are received & only if approved to continue by P.I. (e.g. negative serum pregnancy and eGFR>60). An IV catheter is placed in the antecubital vein to administer an injection of (gadolinium) contrast medium. A coil is placed on each side of the subject's neck while laying flat on a bench, with her upper body inside the MRI scanner. The entire MRI procedure takes approximately 60 minutes.
Observational
Observational Model: Case Control
Time Perspective: Prospective
Not Provided
Retention:   Samples Without DNA
Description:

Lipids, LDL-Buoyancy, Apo-B, Apo-A1 Inflammatory markers: hs-CRP, SAA, IL-6, & TNF-α Vascular Adhesion Markers: VCAM, sICAM

Non-Probability Sample

Pre-menopausal Women

Metabolic Syndrome
Not Provided
  • Women with Metabolic Syndrome

    Pre-menopausal women with Metabolic Syndrome

    Age 35-50 and any 3 of the following:

    Fasting triglycerides ≥ 150 mg/dL, Waist measurement ≥ 35 inches, HDL < 50mg/dL, Fasting glucose ≥ 100mg/dL but <126mg/dL or Blood pressure ≥ 130/85 or taking medication to treat high blood pressure.

  • Non-Metabolic Syndrome (healthy) women

    Non-Metabolic syndrome pre-menopausal women age 35-50

    • Body Mass Index ≤ 25
    • Regular menstrual cycles (occur every 24-35 days)
    • Fasting glucose < 100mg/dL
    • HDL-C ≥ 50mg/dL
    • Waist measurement ≤ 35 inches
    • Fasting triglycerides < 150mg/dL
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
43
July 2013
July 2012   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Pre-menopausal women (age 35-50)

    • still having menstrual periods

Exclusion Criteria:

  • History of diabetes mellitus
  • History of cardiovascular disease (peripheral vascular disease, coronary artery disease, cerebrovascular disease)
  • Serum creatinine >1.2 mg/dL (eGFR <60 ml/min.)
  • Active rheumatologic disease
  • Use of hormonal contraception*
  • Pregnant or planning a pregnancy within the next 3 months
  • Fasting triglycerides ≥ 500 mg/dL
  • Fasting LDL-C ≥ 190 mg/dL
  • Currently taking lipid lowering medications*
  • Currently taking vaso-active (blood pressure) medications*
  • Hypertension: SBP ≥ 140 and or DBP ≥90 mm Hg
  • Chronic use of aspirin (prn use is allowed)
  • Chronic use of non-steroidal anti-inflammatory medications (prn use is allowed)
  • Tobacco use within 3 months of starting study
  • Participation in another clinical trial within the last 30 days
  • MRI specific exclusion criteria:

    • History of claustrophobia
    • History of decrease in kidney function (eGFR <60 ml/min.)
    • History of reaction to a contrast medium or dye used for an MRI, CT Scan, or X-ray
    • History of significant anemia or other blood disease
    • History of seizures
    • MRI-incompatible metal such as internal metal hardware or devices * Drugs within the following classifications are exclusionary: Antilipemics, antilipidemics, beta blockers, ACE inhibitors, angiotensin receptor blockers, diuretics, calcium channel blockers, alpha blockers, nitrates, and all hormonal contraceptives
Female
35 Years to 50 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01068535
35352-A
No
University of Washington
University of Washington
Not Provided
Principal Investigator: Pathmaja Paramsothy, M.D.,M.S. University of Washington
University of Washington
September 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP