Skip to content

Study on the Efficacy and EEG Characteristics of Dexmedetomidine Combined with Esketamine in the Treatment of Adolescent Major Depressive Disorder

Study on the Efficacy and EEG Characteristics of Dexmedetomidine Combined with Esketamine in the Treatment of Adolescent Major Depressive Disorder

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128844
Enrollment
Unknown
Registered
2026-07-27
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Major Depressive Disorder in Adolescents

Interventions

Therapy Group:Intranasal Dexmedetomidine combined with Intravenous Esketamine

Sponsors

Guabgzhou First People‘s Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 18 Years

Inclusion criteria

Inclusion criteria: 1. Aged 12-18 years (inclusive), any sex; 2. Meet DSM-5 criteria for Major Depressive Disorder (MDD), as assessed by a psychiatrist; 3. Current episode duration >= 2 weeks; 4. If suicidal ideation is present, the risk must be classified as non-imminent on the Columbia-Suicide Severity Rating Scale (C-SSRS) (i.e., no immediate high-risk plan or means); 5. Prior antidepressant use is permitted, provided the dosage has been stable for >= 14 days.

Exclusion criteria

Exclusion criteria: 1. Comorbid bipolar disorder, schizophrenia, or other psychiatric disorders; 2. Severe hypertension, bradycardia, conduction block, or recent serious heart disease; 3. Craniocerebral injury or epilepsy; 4. Moderate to severe hepatic/renal impairment; 5. Allergy to anesthetic drugs; 6. Patients currently taking three or more psychotropic medications.

Design outcomes

Primary

MeasureTime frame
Hamilton Depression Rating Scale (HAMD-24) Score;

Secondary

MeasureTime frame
Hamilton Anxiety Rating Scale (HAMA) Score;Columbia-Suicide Severity Rating Scale (C-SSRS) Suicidal Ideation Score;Behavior Rating Inventory of Executive Function (BRIEF) Score;Resting-state and task-state EEG alpha power and alpha/theta ratio;Pittsburgh Sleep Quality Index (PSQI);Vineland Adaptive Behavior Scales (VABS) Score;Adverse Event (AE) Incidence;

Countries

China

Contacts

Public ContactYanlu Ying

Guabgzhou First People‘s Hospital

eyyingyanlu@scut.edu.cn+86 15018467251

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026