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Research on the Efficacy and Mechanism of Magnetic Seizure Therapy in Treatment-Resistant Schizophrenia

Research on the Efficacy and Mechanism of Magnetic Seizure Therapy in Treatment-Resistant Schizophrenia

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400092331
Enrollment
Unknown
Registered
2024-11-14
Start date
2024-11-15
Completion date
Unknown
Last updated
2024-12-02

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

Conditions

Treatment-Resistant Schizophrenia

Interventions

MST group:Combining drug therapy with magnetic seizure therapy.
Drug Treatment group:Antipsychotic Drugs

Sponsors

Nanjing Brain Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1.Diagnosis of schizophrenia according to DSM-5 diagnostic criteria; 2.According to the Treatment Response and Resistance in Psychosis ( TRRIP ): assessment using standardized scales such as PANSS; the severity of the symptoms was at least moderately severe; duration >= 12 weeks; an effective scale was used to assess functional impairment above moderate. Treatment dose >= 600 mg / d chlorpromazine equivalent, treatment time under treatment dose >= 6 weeks, sufficient and sufficient course of treatment with >= 2 different antipsychotics; 3.Age over 16 years old, under 50 years old, gender unlimited; 4.Right-handed; 5.Be able to sign a written informed consent;

Exclusion criteria

Exclusion criteria: 1.Patients with other mental disorders after evaluation by psychiatrists; 2.Patients with severe physical diseases such as brain organic diseases, cardiovascular diseases, tumors and so on; 3.Abnormal laboratory tests affect the efficacy of the study or affect the safety of the subjects; 4.Intracranial metal foreign matters, patients with cardiac pacemakers, cochlear implants, etc; 5.Pregnant, lactating women or those planning to become pregnant during the trial; 6.Patients who had received ECT treatment within 3-6 months, or who had previously received ECT treatment were ineffective; 7.Other situations that the researchers believe are not suitable for participating in the clinical trial;

Design outcomes

Primary

MeasureTime frame
MATRIC Consensus Cognitive Battery, MCCB;Autobiographical Memory Test, AMT;Positive and Negative Syndrome Scale score, PANSS;

Secondary

MeasureTime frame
Treatment Emergent Symptom Scale, TESS;estradiol;luteinizing hormone;progesterone;prolactin;testosterone;follicle stimulating hormone;Changes of brain structure and functional imaging;Richmond Agitation-Sedation Scale, RASS;The Confusion Assessment Method, CAM-ICU;IL-1ß, IL-2, IL-4, IL-5, IL-6, IL-8, IL-10, IL-12p70, IL-17, IFN-?, TNF-a, IFN-a;S-100 protein;blood cells analysis;

Countries

China

Contacts

Public ContactYuxiu Sui

Nanjing Brain Hospital

suiyuxiu@aliyun.com+86 13815895546

Outcome results

None listed

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