- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT00183352
Reproductive Function and Mood in Women With Bipolar Disorder
Reproductive Endocrine Function and Mood Over the Menstrual Cycle of Women Treated for Bipolar Disorder
Descripción general del estudio
Estado
Condiciones
Descripción detallada
Bipolar disorder is a serious condition that can have devastating effects on social and psychological functioning. Evidence suggests that medications for bipolar disorder may influence reproduction function among women. This study will determine reproductive function and mood changes in women who are currently on medication for bipolar disorder.
This study will comprise women with bipolar disorder and age- and body mass index (BMI)-matched healthy controls. Participants will have their reproductive function and mood changes assessed for 3 consecutive menstrual cycles. Daily, participants will report about their mood, sleep patterns, life events, and any psychiatric medications; this information will be entered into a computerized system named ChronoRecord. In addition, participants will measure their basal body temperature and collect their urine every morning to assess for ovulation. Blood collection will occur at study entry and between Days 3 and 6 of every menstrual cycle to determine levels of reproductive hormones. Participants will be asked to fast for 12 hours prior to every blood collection. During the first month of the study, an extra study visit will occur. Participants will undergo a physical exam for determination of excessive hair growth (hirsutism) and BMI. Additionally, insulin resistance will be measured, and participants will be asked to complete a questionnaire that will be used to determine their past and current menstrual function, as well as the reproductive and psychiatric history of their families.
Tipo de estudio
Inscripción (Anticipado)
Contactos y Ubicaciones
Ubicaciones de estudio
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California
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Stanford, California, Estados Unidos, 94305
- Stanford 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
Método de muestreo
Población de estudio
Descripción
Inclusion Criteria for All Participants:
- Have been menstruating for at least 4 years prior to study entry
- Participants must be willing to travel to Stanford University at own expense for study visits
Inclusion Criteria for Bipolar Disorder Participants:
- Participants should have a diagnosis of Bipolar I, Bipolar II, or Bipolar not otherwise specified (NOS), and be under the treatment of a physician who can be contacted in case of an emergency
- Current treatment with any mood-stabilizing agent for a period of at least 3 months (e.g., divalproex sodium, lithium, other mood stabilizer, or atypical antipsychotic)
Inclusion Criteria for Healthy Controls:
- No past or present diagnosis of mental illness
Exclusion Criteria for All Participants:
- Current alcohol or substance abuse or dependence within 6 months prior to study entry
- Meets criteria for another DSM-IV Axis I disorder
- Contraceptive steroid use within 3 months prior to study entry
- Current use of medication that may affect steroid metabolism
- Menopausal
- Endocrine disease such as diabetes or hypothyroidism
- Uncontrolled medical illness
- History of long-term corticosteroid use
- Organic mood disorder
- Pregnancy or breastfeeding within 3 months prior to study entry
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Modelos observacionales: Ecológico o Comunitario
- Perspectivas temporales: Futuro
Cohortes e Intervenciones
Grupo / Cohorte |
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1
Women with bipolar disorder
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2
Women who are healthy controls
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Investigador principal: Natalie L. Rasgon, MD, PhD, Department of Psychiatry and Behavioral Sciences, Stanford University
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
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- R01MH066033 (Subvención/contrato del NIH de EE. UU.)
- SPO# 28571
- DAHBR 96-BHC (Otro número de subvención/financiamiento: National Institute of Mental Health (NIMH))
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .
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