- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT03069911
Trial of OnabotulinumtoxinA for Depression in Parkinson Disease
Randomized Controlled Trial of OnabotulinumtoxinA for Depression in Parkinson Disease
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Depression is a common, but treatable, comorbid condition often seen in persons with Idiopathic Parkinson Disease (iPD). Depression in Parkinson Disease may be hard to treat as patients with iPD may be sensitive to side effect of medication. As a result, other treatments which have better side effects profiles than antidepressants may be equivalent (or better) options.
OnabotulinumtoxinA is a purified formulation of botulinum toxin serotype A which is widely utilized for neurological (and cosmetic) purposes in medicine. OnabotulinumtoxinA has preliminary studies showing it may be beneficial for the treatment of Major Depressive Disorder when given in isolated injections to facial muscles (corrugator and procerus). When given in low doses, onabotulinumtoxinA is thought to have minimal side effects.
The investigators propose that a single treatment onabotulinumtoxinA may improve symptoms of depression in persons with Parkinson Disease over three months compared to placebo. The investigators plan to use both subjective and objective evaluations of depression symptoms and regular physical exams to ensure physical (motor) symptoms of Parkinson Disease do not worsen.
Tipo de estudio
Inscripción (Actual)
Fase
- Fase 1
Contactos y Ubicaciones
Ubicaciones de estudio
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Maryland
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Baltimore, Maryland, Estados Unidos, 21287
- Johns Hopkins University School Of Medicine
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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:
- Written informed consent is obtained in the English language;
- They are a 18 to 95 years old;
- They meet United Kingdom Brain Bank Criteria for probable idiopathic Parkinson disease;
- They meet Diagnostic and Statistical Manual (DSM)-IV criteria for major depressive disorder (MDD) as diagnosed by the M.I.N.I. at screening;
- They are judged by the investigator to have the capacity to understand the nature of the study;
- They are willing to comply with all the requirements of the study;
- They are considered by the investigator to be likely to adhere to the protocol.
Exclusion Criteria:
- They have been treated with onabotulinumtoxinA injected into the facial muscles for any reason in the 3 months prior to screening;
- They have Bipolar Disorder, Post-Traumatic Stress Disorder, a Psychotic Disorder or any other non-unipolar depressive disorder as a principal diagnosis in the 6 months prior to screening;
- They endorse active suicidal ideation at enrollment or during any study visit, or have attempted suicide in the six months prior to screening;
- They have a history of substance abuse or dependence in the 2 months prior to screening;
- They test positive for illicit drugs on urine screen, and this has not been adequately explained to the satisfaction of the investigator
- They are considered to be at significant risk of committing homicide;
- They have an unstable medical condition;
- Women of childbearing potential who are pregnant or are considering becoming pregnant during the length of the study;
- There has been a change in their PD medication or psychotherapy treatment regimen in the 30 days preceding screening;
- They are regarded, for any reason, by the principal investigator as being an unsuitable candidate for the protocol.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Cuadruplicar
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Intervention
One injection of onabotulinumtoxinA (29 units for women and 40 units for men) will be injected into two facial muscles - the corrugator and procerus.
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OnabotulinumtoxinA (29 units for women; 40 units for men) diluted with 0.9% sodium chloride (saline) solution to 40 units per milliliter (mL) (0.725 mL for women, 1 mL for men)
Otros nombres:
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Comparador de placebos: Control
One injection of saline solution will be injected into two facial muscles - the corrugator and procerus.
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0.9% sodium chloride solution (saline) solution injections (0.725mL for women, 1mL for men)
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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Hamilton Rating Scale for Depression (HDRS)
Periodo de tiempo: Baseline and two visits over three months (weeks 6 and 12)
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Improvement on a clinician-rated objective scale for depression as assessed over two weeks (6 weeks and 12 weeks after treatment)
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Baseline and two visits over three months (weeks 6 and 12)
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Clinical Global Impression - Improvement (CGI-I)
Periodo de tiempo: Baseline and two visits over three months (weeks 6 and 12)
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Improvement on a measure of global change from screening to study discontinuation
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Baseline and two visits over three months (weeks 6 and 12)
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Clinical Global Impression - Severity (CGI-S)
Periodo de tiempo: Baseline and two visits over three months (weeks 6 and 12)
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Improvement on measure of global illness severity from screening to study discontinuation
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Baseline and two visits over three months (weeks 6 and 12)
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Beck Depression Inventory II
Periodo de tiempo: Baseline and two visits over three months (weeks 6 and 12)
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Improvement on a participant-rated subjective scale for depression as assessed over two visits
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Baseline and two visits over three months (weeks 6 and 12)
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Clinical Severity Score for Glabellar Frown Lines
Periodo de tiempo: Baseline and two visits over three months (weeks 6 and 12)
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Assessment of change in participant frowning before and after onabotulinumtoxinA injections and relationship with depressive symptoms
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Baseline and two visits over three months (weeks 6 and 12)
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Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
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 (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Síntomas de comportamiento
- Desordenes mentales
- Enfermedades Cerebrales
- Enfermedades del Sistema Nervioso Central
- Enfermedades del Sistema Nervioso
- Trastornos del estado de ánimo
- Trastornos Parkinsonianos
- Enfermedades de los ganglios basales
- Trastornos del movimiento
- Sinucleinopatías
- Enfermedades neurodegenerativas
- Depresión
- Desorden depresivo
- Enfermedad de Parkinson
- Efectos fisiológicos de las drogas
- Agentes neurotransmisores
- Mecanismos moleculares de acción farmacológica
- Agentes del sistema nervioso periférico
- Agentes colinérgicos
- Moduladores de transporte de membrana
- Inhibidores de la liberación de acetilcolina
- Agentes neuromusculares
- Toxinas botulínicas
- Toxinas botulínicas, tipo A
- abobotulinumtoxinA
Otros números de identificación del estudio
- IRB00082708
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Descripción del plan IPD
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
producto fabricado y exportado desde los EE. UU.
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