Skip to content

The study on the efficacy and safety of adjunctive treatment with clobazam in patients with refractory epilepsy and comorbid anxiety

The study on the efficacy and safety of adjunctive treatment with clobazam in patients with refractory epilepsy and comorbid anxiety

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400095079
Enrollment
Unknown
Registered
2024-12-31
Start date
2025-01-01
Completion date
Unknown
Last updated
2025-01-06

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

Conditions

Resistant epilepsy comorbid with anxiety

Interventions

Only one group, for their own before and after the control:Clobazam

Sponsors

Department of Neurology, Affiliated Hospital of Zunyi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Age at enrollment between 16-65 years old (inclusive of boundary values); weight over 50kg;male or female; 2.Patients diagnosed with drug-resistant epilepsy according to the "Chinese Expert Consensus on Drug-resistant Epilepsy" published by the Epilepsy Committee of the Neurology Branch of the Chinese Medical Association in 2015, who visited the Epilepsy Clinic at the Affiliated Hospital of Zunyi Medical University between September 2024 and December 2025; 3.Clinically presenting with anxiety symptoms and meeting the diagnostic criteria for anxiety based on scale scores; 4. A score of 24 or higher on the Mini-Mental State Examination (MMSE); 5. No epileptic status in the 3 months prior to enrollment; 6.Signed informed consent and willing to cooperate with the experiment; 7. Not undergoing treatment for depression or anxiety; 8.Normal blood routine, liver and kidney function, electrolytes, and electrocardiogram (ECG) prior to enrollment

Exclusion criteria

Exclusion criteria: 1.Combined with severe organic diseases, such as cardiovascular and cerebrovascular diseases, etc.; 2.Those with mental disorders; 3. Alcohol dependent or drug abusers; 4.Pregnant or lactating women; 5.Those allergic to the study drugs; 6.Those with severe self-harm, suicidal behavior, and attempts; 7.Patients with abnormal liver and kidney function.

Design outcomes

Primary

MeasureTime frame
Frequency of seizures;Degree of improvement in anxiety.;

Countries

China

Contacts

Public ContactZucai Xu

The Affiliated Hospital of Zunyi Medical University

docxzc@126.com+86 133 6866 3217

Outcome results

None listed

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