Stroke Clinical Trial
— WHIMS-MRIOfficial title:
Effects of Hormone Therapy on Subclinical Neurological Pathology-The WHIMS-MRI Collaborative Study
| NCT number | NCT00739869 |
| Other study ID # | 571 |
| Secondary ID | N01-WH-4-4221 |
| Status | Completed |
| Phase | |
| First received | |
| Last updated | |
| Start date | May 2004 |
| Est. completion date | March 2007 |
| Verified date | May 2024 |
| Source | National Heart, Lung, and Blood Institute (NHLBI) |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Observational |
A silent stroke is a type of stroke that does not produce any severe symptoms, but may slightly affect memory or thinking abilities. Women who take hormone replacement therapy (HRT) may have a higher risk of experiencing a silent stroke than women who do not use HRT. This study will use magnetic resonance imaging (MRI) to determine the prevalence of silent strokes and other changes in brain tissue in women who participated in the Women's Health Initiative Memory Study (WHIMS), a study in which women received HRT, either as estrogen alone or as estrogen and progesterone combined, or placebo.
| Status | Completed |
| Enrollment | 1426 |
| Est. completion date | March 2007 |
| Est. primary completion date | April 2006 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | Female |
| Age group | 65 Years to 90 Years |
| Eligibility | Inclusion Criteria: - Participated in the WHIMS study - Receives medical care at 1 of the 13 WHIMS MRI clinics Exclusion Criteria: - Currently has a pacemaker (either working or non-functioning), intracranial aneurysm clip, neurostimulator, defibrillator, intra-ocular ferrous foreign body (e.g., metal in the eye), or Harrington rods - Currently has a magnetically or electrically activated device, including any of the following items: cochlear implant, transcutaneous electrical nerve stimulation (TENS) unit, implanted pump (insulin or infusion), or a McGee Stapes implant - Potential participants who have the following exclusion criteria may be eligible for participation, based on study staff approval: 1. Metal fragments around critical soft tissue (i.e., shrapnel near spinal cord) 2. Prosthetics 3. Eyelid spring or wire 4. Metallic stent, filter, or coil 5. Breast tissue expander 6. Tattoo or non-removable body piercing 7. Difficulty lying flat 8. Difficulty breathing 9. Claustrophobia |
| Country | Name | City | State |
|---|---|---|---|
| United States | Wake Forest University Health Sciences | Winston-Salem | North Carolina |
| Lead Sponsor | Collaborator |
|---|---|
| National Heart, Lung, and Blood Institute (NHLBI) | Wake Forest University Health Sciences |
United States,
Jaramillo SA, Felton D, Andrews L, Desiderio L, Hallarn RK, Jackson SD, Coker LH, Robinson JG, Ockene JK, Espeland MA; Women's Health Initiative Memory Study Research Group. Enrollment in a brain magnetic resonance study: results from the Women's Health Initiative Memory Study Magnetic Resonance Imaging Study (WHIMS-MRI). Acad Radiol. 2007 May;14(5):603-12. doi: 10.1016/j.acra.2007.02.001. — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Prevalence of silent infarcts in women assigned to HRT versus women assigned to placebo | Measured at a single study visit |
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