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Efficacy and safety of ethosuximide in the treatment of depression: a randomized controlled trial

Efficacy and safety of ethosuximide in the treatment of depression: a randomized controlled trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022765
Enrollment
Unknown
Registered
2019-04-25
Start date
2019-01-01
Completion date
Unknown
Last updated
2019-04-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Major depressive disorder

Interventions

Group 1:Single 500mg ethosuximide treatment
Group 2:Single 1000mg ethosuximide treatment
Group 3:Single 1500mg ethosuximide treatment
Group 4:Single placebo treatment
Group 5:Repeated 1500mg ethosuximide treatment

Sponsors

Chaohu Hospital affiliated to Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Responding to the diagnosis of Major Depressive Disorder according to DSM IV; 2. Introducing a single depressive episode or recurrent unipolar; 3. Absence of treatment with antidepressant during the last 6 months; 4. Informed consent been signed.

Exclusion criteria

Exclusion criteria: 1. Lifetime history of psychotic features, diagnosis of schizophrenia or any other psychotic disorder, or diagnosis of bipolar disorder; 2. Patients judged clinically to be at serious and imminent suicidal or homicidal risk; 3. Women who are either pregnant or nursing; 4. Serious, unstable medical illnesses including hepatic, renal impairment, respiratory (including obstructive sleep apnea, or history of difficulty with airway management during previous anesthetics), cardiovascular (including ischemic heart disease and uncontrolled hypertension), endocrinologic, neurologic (including history of severe head injury), immunologic, or hematologic disease; 5. Clinically significant abnormal findings of laboratory parameters, physical examination, or ECG; 6. Patients who have a positive urine toxicology for illicit substances at screening and within 24 hours of the infusion; 7. Previous recreational use of ketamine.

Design outcomes

Primary

MeasureTime frame
HAMD;MADRS;

Secondary

MeasureTime frame
VAS;HAMA;

Countries

China

Contacts

Public ContactKai Zhang

Chaohu Hospital affiliated to Anhui Medical University

543918@163.com+86 18921104636

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026