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Study on the effect and mechanism of gut microbiota with drug-resistance epilepsy

Study on the effect and mechanism of gut microbiota with drug-resistance epilepsy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400094968
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

Drug-resistant epilepsy

Interventions

Microbiome therapy group:Probiotic intestinal flora transplantation
Control group:Oral treatment with antiepileptic drugs

Sponsors

The First Hospital of Hebei Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Age 12-60 years old, Han nationality; 2. Alone or in combination with 2 first-line antiepileptic drugs to reach the therapeutic dose, still have 2 (or more) seizures per month; 3. The type of seizure is not limited; 4. History of epilepsy greater than 1 year; 5. There was no change in the daily antiepileptic medication taken by the patient during the 3 weeks prior to the baseline period, and the participant agreed to keep the antiepileptic medication unchanged throughout the study; 6. Sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Use of antibiotics, probiotics or prebiotics within 4 weeks; 2. Bowel examination within 4 weeks; 3. Patients who have received physical treatment (electrical, magnetic, sound, light, etc.) for epilepsy within 4 weeks; 4. Have undergone intestinal surgery in the past; 5. Progressive brain disease or serious systemic disease other than epilepsy; 6. Severe depression, anxiety, obsessive-compulsive or other psychiatric diseases or drug or poison abuse; 7. Lactation or pregnancy; 8. Those who have sufficient experience and make a comprehensive judgment that the patient is not suitable for treatment after considering the patient's relevant condition.

Design outcomes

Secondary

MeasureTime frame
Changes in the number of abnormal discharge activities such as spikes and spikes at baseline and at the end of treatment.;

Primary

MeasureTime frame
From the end of treatment to the end of follow-up, the frequency of seizures decreased by 100 points from baseline;

Countries

China

Contacts

Public ContactZhongxin Li

The First Hospital of Hebei Medical University

1040566195@qq.com+86 186 3388 9720

Outcome results

None listed

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