JPRN-UMIN000007794已完成3 期
A sham-controlled, double-blind, parallel-group, randomized trial of repetitive transcranial magnetic stimulation (rTMS) for major depressive disorder, followed by a semi-crossover open trial of rTMS. - A sham-controlled, double-blind, parallel-group, randomized trial of repetitive transcranial magnetic stimulation (rTMS) for major depressive disorder.
Kinkou Hospital, Kanagawa Psychiatric Center0 个研究点目标入组 90 人开始时间: 2012年4月23日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 90
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 75years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1. Absolute contraindications of rTMS (inplanted medical devices or intracranial ferromagnetic material) 2. Relative contraindications of rTMS, including a) pregnancy, b) seizure disorders or paroxysmal EEG abnormality, and c) medications known to lower seizure threshold 3. Other current Axis I disorders 4. Suicidality (Ham-D suicidality score more than 3) 5. Psychotic features during current episode 6. Instability of physical conditions 7. History of neurologic disorders 8. Previous treatments with rTMS and VNS, and treatment history of ECT within a year
研究者
相似试验
招募中
3 期
Study on the efficacy and safety of AT-04 for endometriosisdysmenorrhea heavy menstrual bleedingD004715endometriosisJPRN-jRCTs032230278Koga Kaori50
进行中（未招募）
1 期
A double blind, placebo-controlled, parallel group study to evaluate the efficacy and safety of acetylsalicylic acid combined with pseudoephedrine, compared with acetylsalicylic acid alone, and pseudoephedrine alone, on symptoms of pain and nasal congestion in patients with symptomatic upper respiratory tract infection.asal congestion and pain associated with viral upper respiratory tract infectionMedDRA version: 9.1 Level: LLT Classification code 10046308 Term: Upper respiratory tract infection viral NOSEUCTR2009-011355-46-GBBayer Consumer Care AG
尚未招募
不适用
Clinical investigation on effects of FSFW0121 on appetite and weight management in overweight/obese subjects.CTRI/2021/12/038615Akay Natural Ingredients Pvt Ltd
进行中（未招募）
不适用
A double blind, placebo controlled, parallel group study with an open label reference arm to assess the effects of intravenously administered AIN457 on ozone induced neutrophilia compared to placebo and oral corticosteroid in healthy volunteersHealthy volunteersEUCTR2008-002854-39-DEovartis Pharma Services AG24
进行中（未招募）
不适用
A double blind, placebo controlled, parallel group, multicenter study to assess the duration of action, safety and toleration of differing doses and combinations of immediate and modified release formulations of UK-369,003 and Cialis compared to placebo in adult male subjects with erectile dysfunction. - N/AMale Erectile DysfunctionEUCTR2004-001955-12-DEPfizer Pharma GmbH335