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The Clinical Efficacy of Amantadine on Vegetative State Post-Traumatic Brain Injury

The Clinical Efficacy of Amantadine on Vegetative State Post-Traumatic Brain Injury

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400091956
Enrollment
Unknown
Registered
2024-11-06
Start date
2015-05-26
Completion date
Unknown
Last updated
2024-11-11

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

Conditions

Traumatic brain injury

Interventions

treatment group:the treatment group received amantadine combined with comprehensive rehabilitation treatment.
control group:the control group received comprehensive rehabilitation treatment.

Sponsors

The First Hospital of Jilin University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) Patients with vegetative state after brain injury for 4-16 weeks; (2) Age 18-65 years old, without penetrating brain injury and with stable vital signs; (3) CRS-R score = 8 points, DRS score = 20 points, Rancho Los Amigos I-III; (4) Sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Those whose vital signs have not stabilized or whose condition has worsened during the acute phase; (2) Individuals with poor control of seizures; (3) Complicated with severe kidney disease; (4) Individuals with severe hydrocephalus; (5) Those who take other psychotropic drugs for treatment; (6) Individuals who are allergic to amantadine.

Design outcomes

Primary

MeasureTime frame
Coma Recovery Scale-Revised score;

Secondary

MeasureTime frame
Disability Rating Scale score;Rancho Los Amigos Levels of Cognitive Functioning ;

Countries

China

Contacts

Public ContactZhenlan Li

The First Hospital of Jilin University

zhenlan@jlu.edu.cn+86 159 4305 3720

Outcome results

None listed

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