Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
2000 participants
OBSERVATIONAL
2018-04-24
2027-12-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Ultrabrief Pulsewidth Electroconvulsive Therapy (ECT)
NCT00870805
Brain Changes in Severely Depressed Patients Before and After Treatment With Electroconvulsive Therapy
NCT02715986
Electroconvulsive Therapy (ECT) for Elderly Patients With Major Depression
NCT01559324
Cognitive Effects Associated With Hippocampal Neurogenesis Induced by ECT in the Treatment of Depression
NCT06661616
Study of Transcranial Direct Current Stimulation (tDCS) as add-on Treatment for Resistant Major Depression
NCT01428804
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Centre Hospitalier Henri Laborit
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
CHU d'Angers : Site Larrey
Angers, , France
Clinique Mirambeau
Anglet, , France
CHS de Montfavet
Avignon, , France
CH Cote Basque
Bayonne, , France
Fondation bon sauveur
Bégard, , France
Centre de crise Esquirol
Caen, , France
CHU Gabriel Montpied
Clermont-Ferrand, , France
CH La Chartreuse
Dijon, , France
Clinique du domaine de Vontes
Esvres-sur-Indre, , France
Clinique de Pen-An-Dalar
Guipavas, , France
CUMP Océan Indien
La Réunion, , France
CH Marius Lacroix
La Rochelle, , France
Césame
Les Ponts-de-Cé, , France
CH de Mayenne
Mayenne, , France
CHR Metz-Thionville
Metz, , France
CH psy de la drôme Vivarais
Monteléger, , France
CHS la Colombiere
Montpellier, , France
CH Saint Roch
Nice, , France
CH Sainte Anne
Paris, , France
CH Henri Laborit
Poitiers, , France
CHI Redon-Carentoir
Redon, , France
CH Guillaume Regnier
Rennes, , France
CH du Rouvray
Rouen, , France
Epsm du Morbihan
Saint-Avé, , France
Clinique Villa du Parc
Saujon, , France
CH Civil 1
Strasbourg, , France
CH Nord Deux Sèvres
Thouars, , France
CHITS CH Sainte Musse
Toulon, , France
CH Purpan
Toulouse, , France
CPU de Tours
Tours, , France
Countries
Review the countries where the study has at least one active or historical site.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Marine ROZET, MD
Role: primary
Christophe DAUDET, MD
Role: primary
Hosni EL OUAHCHI, MD
Role: primary
Antoine OLIVEIRA, MD
Role: primary
Claire BERNARD, MD
Role: primary
Pierrick LEBAIN, MD
Role: primary
Role: backup
Clémence MOREAU, MD
Role: primary
Role: backup
Jean-Claude GIROD, MD
Role: primary
Isabelle RAMAGE, MD
Role: primary
Erwan LUVEN, MD
Role: primary
Erick GOKALSING, MD
Role: primary
Anne-Isabelle BOUYER, MD
Role: primary
Mathilde SIX, MD
Role: primary
Pascal LE VAOU, MD
Role: primary
Pierre COURVOISIER, MD
Role: primary
Jérome ATTAL, MD
Role: primary
Laurent GUGENHEIM, MD
Role: primary
Marion PLAZE, MD
Role: primary
Sidi-Mohammed BENSENANE, MD
Role: primary
Dominique DRAPIER, MD
Role: primary
Maud ROTHARMEL, MD
Role: primary
François-Alexis RICHARD, MD
Role: primary
Olivier DUBOIS, MD
Role: primary
Atifa KORICHE, MD
Role: primary
Role: backup
Salima BRAIK, MD
Role: primary
Jean-Luc BARTOLI, MD
Role: primary
Antoine YRONDI, MD
Role: primary
Maxime BONNIN, MD
Role: primary
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2035305v1
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.