2/2 Collaborative Study: Testosterone Augmentation in Women

2/2 合作研究：女性睾酮水平增强

基本信息

批准号：
8875769
负责人：
LINDA L CARPENTER
金额：
$ 21.11万
依托单位：
BUTLER HOSPITAL (PROVIDENCE, RI)
依托单位国家：
美国
项目类别：
财政年份：
2013
资助国家：
美国
起止时间：
2013-07-24 至 2016-11-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8875769
关键词：
Academic Medical Centers Address Adverse effects Affect Androgens Antidepressive Agents Area Arousal Collaborations Data Data Analyses Depressed mood Disease remission Dose Endocrinology Fatigue Female Future Glycols Health Hormones Hospitals Intervention Intervention Studies Joints Libido Major Depressive Disorder Mental Depression Multicenter Trials Patients Pharmaceutical Preparations Physiological Physiological Processes Placebos Population Postmenopause Psychiatrist Psychiatry Public Health Quality of life Randomized Controlled Trials Recording of previous events Recruitment Activity Research Research Domain Criteria Research Personnel Residual state Resistance Sample Size Sampling Selective Serotonin Reuptake Inhibitor Serotonin Uptake Inhibitors Severities Sex Functioning Sexual Dysfunction Site Study Subject Symptoms Testing Testosterone Therapeutic Validation Woman base career data management depressive symptoms double-blind placebo controlled trial drug candidate effective therapy efficacy testing experience hormone therapy improved interest multidisciplinary novel open label patient oriented research randomized placebo controlled trial response suicidal risk treatment-resistant depression

项目摘要

DESCRIPTION (provided by applicant): Major depressive disorder is a significant public health problem, disproportionately affecting women. Approximately 70% of patients do not respond or only partially respond to standard SSRI treatment despite adequate dosing. In our open-label pilot data, two-thirds of women with major depressive disorder who were resistant or partially resistant to antidepressants achieved a response to very low-dose, physiologic transdermal testosterone administration; one-third of women treated achieved remission after 8 weeks of therapy, with no hyperandrogenic side effects. We propose a collaborative, randomized, placebo-controlled trial to determine whether larger, multi-center trials are indicated to investigate whether low-dose testosterone is an efficacious and well-tolerated augmentation strategy in women with major depressive disorder and SSRI partial/nonresponse. We propose a collaborative, multidisciplinary study from two academic medical centers in order to increase sample size, accelerate recruitment and increase sample diversity.

描述（由申请人提供）：重度抑郁症是一个重大的公共卫生问题，对妇女的影响不成比例。大约70％的患者尽管有足够的给药，但仅对标准SSRI治疗反应反应或仅部分反应。在我们的开放标签试验数据中，三分之二的患有抗抑郁药具有抗性或部分抗性抗抑郁药的妇女对非常低剂量的生理透皮睾丸激素给药的反应得到了反应。三分之一接受治疗的妇女在治疗8周后获得了缓解，没有过度雄激素的副作用。我们提出了一项协作，随机的安慰剂对照试验，以确定是否指示了较大的多中心试验研究低剂量睾丸激素是否是具有重度抑郁症和SSRI部分/无反应女性的有效且耐受性的增强策略。我们提出了来自两个学术医疗中心的合作，多学科研究，以增加样本量，加速招聘并增加样本多样性。