Healthy Clinical Trial
Official title:
Effects of Hormone Therapy on Vascular Inflammation and Compliance
This study will determine the effects of hormone replacement therapy (estrogen alone or
estrogen and progesterone) on the walls of arteries in postmenopausal women. Inflammation
and stiffness of artery walls are two risk factors for atherosclerosis-deposits of fatty
substances (plaques) that can block the vessel, causing a heart attack or stroke. Estrogen
raises the levels of certain substances in the blood that cause vessel inflammation and
lowers the levels of others. This study will measure the net effects of estrogen on artery
wall inflammation and stiffness.
Postmenopausal women in good health may participate in this study. Volunteers will be
screened for eligibility with a complete medical history, heart examination, and blood
tests. Participants will be randomly assigned to receive either: 1) hormone therapy
(estradiol 2 mg daily alone for women who have had a hysterectomy or estradiol plus
micronized progesterone 200 mg daily for women with an intact uterus); or 2) placebo
(look-alike pills that contain no active drug). Women in both groups will take pills for 3
months, then no pills for 1 month, and then will crossover to the alternate therapy for 3
months (i.e., those in the original placebo group will take hormones, and those in the
hormone group will take placebo). At the end of each 3-month treatment period, participants
will undergo the following procedures to assess blood vessel inflammation and stiffness:
1. Blood tests - 60 cc (about 2 ounces) of blood will be drawn to measure levels of
hormones, cholesterol, and substances in the blood that indicate inflammation of the
vessels.
2. Ultrasonography - an ultrasound probe will be applied gently on the neck to image the
right and left carotid arteries (arteries in the neck that lead to the brain). During
the procedure, the heart's electrical activity will also be monitored with an
electrocardiogram and a blood pressure cuff will be wrapped around the arm to obtain
blood pressure measurements every 5 minutes.
3. Magnetic resonance imaging (MRI) - Images of the carotid arteries are taken while the
volunteer lies on a table in a narrow cylinder containing a magnetic field. A padded
sensor called an MRI coil is placed over the neck and earplugs are placed in the ears
to muffle the loud noise of the machine during scanning. During the second half of the
exam, gadolinium is injected through a catheter (thin, flexible tube) inserted into a
vein. Gadolinium is a contrast agent that is used to brighten the scan images.
Information from this study will increase knowledge about the effects of estrogen on vessel
wall inflammation. As such, it may be used in the future to help guide decisions about
chronic hormone replacement therapy in postmenopausal women.
Status | Completed |
Enrollment | 25 |
Est. completion date | January 2002 |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Female |
Age group | N/A and older |
Eligibility |
Ability to comprehend or unwillingness to sign the consent form. No use of estrogen therapy within 2 months of this study. No history of breast cancer, uterine cancer, or estrogen-dependent tumor. No history of deep vein thrombosis or pulmonary embolus. No cigarette smokers (within 2 years). No diabetes mellitus (FBS greater than 120 mg/dL). Triglycerides less than 400 mg/dL. Blood pressure less than 160/90 without antihypertensive therapy. No history of coronary artery disease. No history of carotid artery disease or stroke. No history of pancreatitis. No history of claustrophobia. No history of involuntary motion disorder. Specific MRI exclusion criteria (i.e., no pacemaker, no cochlear implants, no AICD, no internal infusion pump, no metal implants or clips in field of view). No systemic inflammatory disorder (e.g., rheumatoid arthritis, periarteritis nodosa, systemic lupus erythromatosus, temporal arteritis). Must not have a need for chronic aspirin or NSAID therapy. |
Endpoint Classification: Safety/Efficacy Study, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | National Heart, Lung and Blood Institute (NHLBI) | Bethesda | Maryland |
Lead Sponsor | Collaborator |
---|---|
National Heart, Lung, and Blood Institute (NHLBI) |
United States,
Cushman M, Legault C, Barrett-Connor E, Stefanick ML, Kessler C, Judd HL, Sakkinen PA, Tracy RP. Effect of postmenopausal hormones on inflammation-sensitive proteins: the Postmenopausal Estrogen/Progestin Interventions (PEPI) Study. Circulation. 1999 Aug 17;100(7):717-22. — View Citation
Hulley S, Grady D, Bush T, Furberg C, Herrington D, Riggs B, Vittinghoff E. Randomized trial of estrogen plus progestin for secondary prevention of coronary heart disease in postmenopausal women. Heart and Estrogen/progestin Replacement Study (HERS) Research Group. JAMA. 1998 Aug 19;280(7):605-13. — View Citation
Koh KK, Bui MN, Mincemoyer R, Cannon RO 3rd. Effects of hormone therapy on inflammatory cell adhesion molecules in postmenopausal healthy women. Am J Cardiol. 1997 Dec 1;80(11):1505-7. — View Citation
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