Severe Depression

2

Review clinical trials related to Severe Depression. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Nebulized Ketamine for the Treatment of Major Depressive Disorder

This is a double-blind active placebo controlled clinical trial for individuals with moderate to severe depression. The purpose of this study is to assess if nebulized ketamine can reduce depressive symptoms.

Participants needed: 40
Trial details
Phase: Phase 3Age: 18-88Biological sex: AllType: InterventionalSponsor: Theresa Jacob, PhD, MPHUpdated: Apr 24, 2026Locations: 1
Eligibility criteria

All individuals 18 years and older with a Montgomery-Asberg Depression Rating Sc... [+2]

Adult patients with an allergy to Ketamine [+14]

Status: Recruiting

At-Home tDCS as Maintenance Therapy

The primary purpuse of this pilot study is to find out whether a home-based transcranial direct current stimulation (tDCS) program is feasible and well tolerated as maintenance therapy and whether there are early signs that it helps maintain the clinical clinical benefits achieved during successful acute inpatient treatment. Participant population: Adults (18+) with depressive disorder who had already improved/stabilized after acute treatment at our clinic (esketamine, repetitive transcranial magnetic stimulation , or electroconvulsive therapy). Main questions: Feasibility: Do participants reliably complete the home program and stay in the study? Preliminary effectiveness: Do improvements of depressive symptoms hold up over the 4-week treatment and 2-week follow-up (based on self-report and clinician-rated scales)? Participants receive standardized instruction from trained staff and a portable tDCS device (with cap and small sponge electrodes) and complete 20 home sessions over 4 weeks (5 per week), each 30 minutes at a very low current (2 mA); the device gently ramps current up/down for comfort. During treatment, participants use a smartphone app with step-by-step guidance and reminders; sessions are automatically logged. They will also fill out short weekly self-rating questionnaires and join brief phone check-ins every 2 weeks. Where: Department and Outpatient Clinic of Psychiatry and Psychotherapy, Klinikum rechts der Isar, Technical University of Munich Safety \& data privacy: The device monitors electrode contact and pauses automatically if contact is poor. Typical sensations can include mild tingling or redness. The app stores anonymized session data so the care team can track progress; no personal data are exchanged between the app and the stimulator, and access is via a secure clinical portal.

Participants needed: 30
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Technical University of MunichUpdated: Dec 8, 2025Locations: 2
Eligibility criteria

Adults (≥18 years). [+3]

Currently in the acute treatment phase of an affective disorder and non-response... [+4]