Minimally Invasive Surgical Treatment Versus Medical Management for Stroke Patients With Atrial Fibrillation
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Florida
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Gainesville, Florida, Estados Unidos, 32610
- University of Florida
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Patients with a history of stroke and paroxysmal, persistent or permanent AF.
- Ischemic stroke or TIA with documented paroxysmal or persistent atrial fibrillation. A TIA will meet inclusion criteria as a sudden-onset focal neurological symptom or sign lasting at least 10 minutes but less than 24 hours with or without evidence of acute brain ischemia on diffusion weighted MRI imaging.
- Eligible symptoms INCLUDE hemiplegia or hemiparesis, monoplegia, or language disturbance other than isolated dysarthria.
- Symptoms that will NOT QUALIFY AS TIA INCLUDE transient monocular blindness in both eyes, dysarthria, vertigo,isolated sensory symptoms, confusion, memory loss, nonspecific complaints of dizziness, or syncope.
Exclusion Criteria:
- Recent stroke (< 1 month).
- Age < 18 or > 80 years; Ejection Fraction < 25%• Presence of left atrial appendage thrombus on CT or echocardiography
- Previous empyema or thoracic surgery, preventing access to the pulmonary veins via thoracoscopy.
- Left Atrial Diameter > 55mm.
- Contraindication to anticoagulation with Coumadin.
- Mitral insufficiency (> 2+)
- • • Contraindications to MRI
- •Artificial heart valve prosthesis
- Aneurysm clips
- Implanted drug infusion device or pump
- Any type of neurotranstimulator
- Any type of bone growth stimulator
- Cochlear implants or inner ear prosthesis
- Any intravascular coils, filters, or stents
- Shrapnel or bullets
- Other metallic implants or devices specify which
- Permanently tattooed eyeliner
- Are you pregnant or suspect to be pregnant?
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Comparador activo: Minimally Invasive Surgery
Thumb sized incisions are made on each sides of the chest wall where instruments are placed in the chest to perform the surgery.
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Small thumb sized incisions are made on each side of the chest wall where instruments are inserted for the purpose of completing the surgery.
Otros nombres:
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Comparador activo: Medical Therapy
Patients are treated with rhythm and rate control medications.
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Patients are treated with rhythm and rate control medications.
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Quality of Life RAND 36-Item Health Survey
Periodo de tiempo: Change in baseline, 3 month, and 6 month
|
Compare quality of life of patient satisfaction between the surgery and or the medication in stroke patients with AF (atrial fibrillation). The RAND 36-Item Health Survey taps eight health concepts: physical functioning, bodily pain, role limitations due to physical health problems, role limitations due to personal or emotional problems, emotional well-being, social functioning, energy/fatigue, and general health perceptions. It also includes a single item that provides an indication of perceived change in health. Note that all items are scored so that a high score defines a more favorable health state. In addition, each item is scored on a 0 to 100 range so that the lowest and highest possible scores are 0 and 100, respectively. Scores represent the percentage of total possible score achieved. Items in the same scale are averaged together to create the 8 scale scores which will have a 0 to 100 range. |
Change in baseline, 3 month, and 6 month
|
Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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STAI-FormY-1 Questionnaire (State-Trait Anxiety Inventory)
Periodo de tiempo: Change in baseline, 3 month, and 6 month
|
Compare quality of life of patient satisfaction between the surgery and or the medication in stroke patients with AF (atrial fibrillation).
Scores range from 20 to 80, with higher scores correlating with greater anxiety.
|
Change in baseline, 3 month, and 6 month
|
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STAI-Form-Y2 Questionnaire (State-Trait Anxiety Inventory)
Periodo de tiempo: Change in baseline, 3 month, and 6 month
|
Compare quality of life of patient satisfaction between the surgery and or the medication in stroke patients with AF (atrial fibrillation).
Scores range from 20 to 80, with higher scores correlating with greater anxiety.
|
Change in baseline, 3 month, and 6 month
|
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Montreal Cognitive Assessment (Moca)
Periodo de tiempo: Change in baseline, 3 month, and 6 month
|
Compare quality of life of patient satisfaction between the surgery and or the medication in stroke patients with AF (atrial fibrillation).
The score is 0 - 30 point test with the higher the score the better cognitive function.
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Change in baseline, 3 month, and 6 month
|
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Directed Fluency; Cowa (Controlled Oral Word Association Test)
Periodo de tiempo: Change in baseline, 3 month, and 6 month
|
Compare quality of life of patient satisfaction between the surgery and or the medication in stroke patients with AF (atrial fibrillation).
The participant is asked to name as many words as possible beginning with a letter, excluding proper nouns, for one minute and this procedure is repeated three times.
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Change in baseline, 3 month, and 6 month
|
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Hopkins Verbal Learning Test Version A
Periodo de tiempo: Change in baseline, 3 month, and 6 month
|
Compare quality of life of patient satisfaction between the surgery and or the medication in stroke patients with AF (atrial fibrillation).
This test measures word recognition.
12 words are read to the subject and they have to repeat as many as they can recall.
There are 4 trials, each with 12 total possible words.
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Change in baseline, 3 month, and 6 month
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Stroop Color Test
Periodo de tiempo: Change in baseline, 3 month, and 6 month
|
Compare quality of life of patient satisfaction between the surgery and or the medication in stroke patients with AF (atrial fibrillation). Only 9 patients in the minimally invasive surgery arm completed the stroop color test, and only 6 patients in the medical therapy group completed the stroop color test. In this test, subjects are asked to read a list of color words. 100 is the maximum amount of correct responses per trial. |
Change in baseline, 3 month, and 6 month
|
|
Wtar (Wechsler Test of Adult Reading) Word List
Periodo de tiempo: Baseline
|
Compare quality of life of patient satisfaction between the surgery and or the medication in stroke patients with AF (atrial fibrillation). The WTAR is composed of 50 irregularly spelled words and takes approximately 10 minutes to complete. The examiner begins by presenting the first word card and prompting the patient for a single pronunciation of the word. This procedure continues through all 50 word cards and is discontinued if the patient provides 12 consecutive incorrect pronunciations. Each correct pronunciation is given a score of 1, with 50 as the maximum raw score. |
Baseline
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Stroop Word Test
Periodo de tiempo: Change in Baseline, 3 month, and 6 month
|
Compare quality of life of patient satisfaction between the surgery and or the medication in stroke patients with AF (atrial fibrillation). Only 9 patients in the minimally invasive surgery arm completed the stroop word test, and only 6 patients in the medical therapy group completed the stroop word test. In this test, subjects are asked to read a list of words. 100 is the maximum amount of correct responses per trial. |
Change in Baseline, 3 month, and 6 month
|
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Directed Fluency, Animals
Periodo de tiempo: Change in Baseline, 3 month, and 6 month
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Compare quality of life of patient satisfaction between the surgery and or the medication in stroke patients with AF (atrial fibrillation).
The participant is asked to name as many animals as possible beginning with a letter, for one minute.
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Change in Baseline, 3 month, and 6 month
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Thomas Beaver, MD, University of Florida
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 433-2009
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