🔎 Trials Near Me

Inicio › Trastorno depresivo mayor › Connecticut

Ensayos clínicos de Trastorno depresivo mayor en Connecticut

15 estudios sobre Trastorno depresivo mayor buscan participantes en Connecticut.

Ciudades en Connecticut

Texto oficial del estudio (inglés)

A Study of a Deuterated Psilocin Analog (CYB003) in Humans With Major Depressive Disorder

  • Yale School of Medicine - Yale Program for Psychedelic Science, New Haven
ReclutandoFase 3
Edades de 18 a 85 · Todos los sexos · Actualizado el 13 nov 2026 · NCT06793397

A Study to Evaluate the Efficacy and Safety of SPT-300 (GlyphAllo) in Participants With Major Depressive Disorder, With or Without Anxious Distress (BUOY-1 Study)

  • Seaport Investigator Site, Cromwell
ReclutandoFase 2
Edades de 18 a 65 · Todos los sexos · Actualizado el 10 nov 2026 · NCT07065240

A Study of Brenipatide in Adult Participants With Major Depressive Disorder

  • Yale University School of Medicine, New Haven
ReclutandoFase 3
Edades de 18 a 75 · Todos los sexos · Actualizado el 4 nov 2026 · NCT07412756

Phase 3 Study of Adjunctive Treatment With Seltorexant in Adult and Elderly Participants With Major Depressive Disorder and Insomnia Symptoms

  • UConn Health Center, Farmington
ReclutandoFase 3
Edades de 18 a 74 · Todos los sexos · Actualizado el 3 nov 2026 · NCT06559306

A Study to Evaluate the Efficacy and Safety of Esketamine for Reduction of Symptoms of Major Depressive Disorder

  • Yale Child Study Center, New Haven
ReclutandoFase 3
Edades de 12 a 17 · Todos los sexos · Actualizado el 3 nov 2026 · NCT07227454

Study of Lumateperone as Adjunctive Therapy in the Treatment of Patients With Major Depressive Disorder

  • University of Connecticut Health Center, Farmington
ReclutandoFase 3
Edades de 18 a 65 · Todos los sexos · Actualizado el 3 nov 2026 · NCT05850689

Long-Term Study to Assess the Safety and Tolerability of NBI-1065845 as an Adjunctive Treatment in Participants With Major Depressive Disorder (MDD)

  • Neurocrine Clinical Site, Cromwell
  • Neurocrine Clinical Site, Farmington
ReclutandoFase 3
Edades de 18 en adelante · Todos los sexos · Actualizado el 2 nov 2026 · NCT06966401

Double-blind, Placebo-controlled Study in Adults With Major Depressive Disorder

  • CT Clinical Research, Cromwell
ReclutandoFase 2
Edades de 18 a 70 · Todos los sexos · Actualizado el 28 oct 2026 · NCT07226661

A Study to Evaluate the Maintenance Effect of Osavampator as an Adjunctive Treatment in Participants With Major Depressive Disorder (MDD)

  • Neurocrine Clinical Site, New Haven
ReclutandoFase 3
Edades de 18 en adelante · Todos los sexos · Actualizado el 22 oct 2026 · NCT07196501

Zelquistinel or Placebo for the Reduction of Symptoms of Major Depressive Disorder

  • University of Connecticut School of Medicine Psychiatry Department, Farmington
ReclutandoFase 2
Edades de 18 a 64 · Todos los sexos · Actualizado el 3 ago 2026 · NCT06547489

The Impact of AMPA Receptor Blockade on Ketamine's Anti-Suicidal Effects

  • VA Connecticut Healthcare System, West Haven
ReclutandoFase 2
Edades de 21 a 65 · Todos los sexos · Actualizado el 6 may 2026 · NCT05786066

Alpha-Amino-3-Hydroxy-5-Methyl-4- Isoxazole Propionic Acid Receptor Components of the Anti-Depressant Ketamine Response

  • Yale University, New Haven
ReclutandoFase 1
Edades de 18 a 60 · Todos los sexos · Actualizado el 6 may 2026 · NCT05915013

Imaging Depression in Parkinson's Disease

  • Yale University, New Haven
ReclutandoFase 2Se aceptan voluntarios sanos
Edades de 40 a 80 · Todos los sexos · Actualizado el 10 mar 2026 · NCT06402955

Biomarkers/Biotypes, Course of Early Psychosis and Specialty Services

  • Hartford Hospital, Hartford
ReclutandoEstudio observacional
Edades de 18 a 40 · Todos los sexos · Actualizado el 10 mar 2026 · NCT06740383

Study of ABX-002 for the Adjunctive Treatment of Major Depressive Disorder (AMPLIFY)

  • Autobahn Site #122, Cromwell
ReclutandoFase 2
Edades de 18 a 65 · Todos los sexos · Actualizado el 20 ene 2026 · NCT06633016

De ClinicalTrials.gov, datos obtenidos el 15 nov 2026. Cada estudio establece sus propios criterios de elegibilidad; el equipo del estudio decide quién puede participar.