A trial to look for effect of supplemental High-Definition Transcranial Direct Current Stimulation in Treatment of Depressio
- Conditions
- Health Condition 1: F332- Major depressive disorder, recurrent severe without psychotic featuresHealth Condition 2: F331- Major depressive disorder, recurrent, moderateHealth Condition 3: F32- Major depressive disorder, singleepisode
- Registration Number
- CTRI/2024/02/062752
- Lead Sponsor
- Paramjeet Singh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1)Aged 18 to 50 years
2)Sex: male or female
3)Diagnosis of depression (F32, F33) as per ICD-10-DCR
4)Score of 14 or above on HAM-D
5)Provides written informed consent for participation in the study.
1)Presence of any other psychiatric disorder, organic mental disorder, or mental retardation.
2)Known substance dependence other than caffeine or nicotine.
3)Presence of suicide attempts, high risk for suicide, psychotic symptoms or catatonia in current episode
4)Presence of unstable medical condition requiring urgent priority management
5)Has received electro-convulsive therapy or any other neuro-stimulation in last three months
6)Patients with metal in cranium, pacemaker in-situ, history of significant traumatic brain injury, epilepsy or cerebrovascular accident
7)Pregnant or breast-feeding mothers
8)Presence of skin problems, such as dermatitis, psoriasis or eczema over the scalp
9)History of serious adverse event following transcranial electric or magnetic stimulation in the past.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method