ISRCTN16299848已完成未知
An 8-week randomised controlled trial with 16-week follow-up of cupping therapy combined with SSRIs in patients with depression
Beijing Hospital of Traditional Chinese Medicine Affiliated to Capital Medical University0 个研究点目标入组 72 人开始时间: 2018年3月27日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 72
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
- 性别
- All
入选标准
- •1. Diagnosis of depression using the International Classification of Disease (10th version) (ICD-10)
- •2. Aged 18-65 years
- •3. Moderate or severe depression with a score of =17 on HAMD-17
- •4. Current treatment with SSRIs or no medication
- •5. No cupping therapy during the previous 2 weeks
- •6. Patients agree to participant in this trial and assign the informed consent.
排除标准
- •1. Difficulty in communication
- •2. Severe suicidal risk (HAMD-17 suicidal item score=4)
- •3. History of dementia
- •4. History of bipolar disorder, schizophrenia or have obvious psychotic symptoms.
- •5. History of alcohol or drug abuse within 12 months
- •6. Pregnancy or lactation
研究者
相似试验
尚未招募
2 期
Atorvastatin for treatment of acute inflammation in newly diagnosed children with Crohn’s diseaseCrohn's diseaseOral and Gastrointestinal - Crohn's diseaseACTRN12612000129886Royal Children's Hospital60
尚未招募
不适用
Effect of 8-week prebiotic supplementation on gut health in Prosthetic Joint Infection patientsProsthetic Joint InfectionGut DysbiosisInfection - Studies of infection and infectious agentsDiet and Nutrition - Other diet and nutrition disordersMusculoskeletal - Other muscular and skeletal disordersSurgery - Other surgeryInflammatory and Immune System - Other inflammatory or immune system disordersACTRN12623001273673Royal Adelaide Hospital50
进行中(未招募)
不适用
An 8 week extension to a randomized, double-blind, parallel group, active-controlled, multi-center, 14 week study to evaluate the effectiveness of a valsartan versus anamlodipine treatment strategy in achieving blood pressure control in patients with stage 1 or stage 2 hypertension or uncontrolled on present monotherapy - NDEssential hypertensionMedDRA version: 6.1Level: PTClassification code 10015488EUCTR2005-001258-26-ITOVARTIS FARMA1,244
招募中
不适用
An 8-week, randomized, double-blind, placebo-controlled clinical trial for the evaluation of the efficacy and safety of probiotics NVP-1704 on sleep improvementMental and behavioural disordersKCT0009096Seoul National University Bundang Hospital120
已完成
Unknown
Human study of Theracurmin for verification of anti-oxidant effectKCT0008731Seoul National University120
