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Clinical efficacy and neuromechanism of drug combination with rTMS in schizophrenia and depression

Clinical efficacy and neuromechanism of drug combination with rTMS in schizophrenia and depression

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100041876
Enrollment
Unknown
Registered
2021-01-09
Start date
2021-01-20
Completion date
Unknown
Last updated
2021-03-30

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

Conditions

Schizophrenia

Interventions

Intervention group-Schizophrenia:Drug therapy combined with rTMS intervention
Control group-Schizophrenia:Drug therapy
Intervention group-Depression:Drug therapy combined with rTMS intervention
Control group-Depression:Drug therapy

Sponsors

The First Affiliated Hospital of Air Force Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: (1) Diagnosed by a clinical psychiatrist and meeting the DSM-V diagnostic criteria for schizophrenia and depression; (2) In the positive and negative symptoms scale (PANSS) for schizophrenic patients, there were at least 1 > 3 points and P3 hallucination > 3 points in the 4 items (degree of paranoia) of P1 delusion, P5 exaggeration, P6 paranoia/murder and G9 abnormal thinking, which were classified as positive symptoms group;Negative symptom score >18 points, classified as negative symptom group; (3) Hamilton depression scale (hamd-17) total score > 18 for patients with depression; (4) According to the patient's condition, amesulfapidyl tablets and Venlafaxine hydrochloride sustained-release capsules should be selected during the treatment of schizophrenia and depression; (5) Aged 18-50 years, Han nationality, right-handed; (6) Volunteer to participate in the experiment and cooperate, and give informed consent by myself or family members;(7) Education above junior high school level; (8) Onset or course of disease less than 3 years; (9) Antipsychotic drugs were not used in at least 5 half-lives of the drugs before enrollment, and the drug treatment dose was stable at a certain level; (10) At least 4 weeks in the stable period of disease.

Exclusion criteria

Exclusion criteria: (1) Those with brain organic diseases and serious physical diseases such as endocrine system; (2) Intestinal organic lesions were confirmed by relevant auxiliary examinations; (3) women during pregnancy and breastfeeding; (4) A history of alcohol and drug dependence; (5) A history of manic or hypomanic episodes; (6) Depressive episodes accompanied by psychotic symptoms; (7) Electroconvulsive therapy; (8) Persons with impulsive tendencies such as severe suicide, self-injury or wounding; (9) Did not take drugs such as swelling agent, antidiarrid, antibiotic, spasmodic, probiotics and so on within one month; (10) BMI greater than or equal to 32.

Design outcomes

Primary

MeasureTime frame
PNASS;HAMD;MCCB;

Countries

China

Contacts

Public ContactWang Huaning

The First Affiliated Hospital of Air Force Medical University

wanghuan88@163.com+86 13609161341

Outcome results

None listed

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