Clinical Multi-center Study of Mitochondrial Brain Protective Agent Idebenone in the Prevention of Post-stroke Epilepsy

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
SUMMARY

According to the random number table, all patients were divided into short-term treatment group, long-term treatment group and non-intervention stroke control group according to the proportion of (1:1:1) epilepsy disease modifier idebenone. Patients in the short-term treatment group will take idebenone for a total course of 14 days (acute period) after stroke, and patients in the long-term treatment group will take idebenone for a total course of 3 months after stroke.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Patients admitted to hospital within 24 hours of stroke symptoms and diagnosed with stroke (including cerebral infarction, cerebral hemorrhage, subarachnoid hemorrhage, intracranial venous sinus thrombosis, etc.) after relevant examinations;

• Able to cooperate with the inspection;

• Sign the informed consent form.

Locations
Other Locations
China
Xiangya Hospital, Central South University
RECRUITING
Changsha
Contact Information
Primary
Li Feng, PhD
fenglihx@163.com
86-13873123853
Time Frame
Start Date: 2023-07-05
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 2700
Treatments
Experimental: Group A: Idebenone short-term treatment group
The patient received oral idebenone 30 mg three times a day after stroke for a total course of 14 days (acute phase).
Experimental: Group B: Idebenone long-term treatment group
The patient will be treated with oral idebenone 30 mg three times a day after stroke for a total course of 3 months.
Related Therapeutic Areas
Sponsors
Leads: Xiangya Hospital of Central South University

This content was sourced from clinicaltrials.gov