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Anti-epilepsy drugs prophylaxis in cranioplasty for patients with skull defection: A prospective randomized controlled study

Anti-epilepsy drugs prophylaxis in cranioplasty for patients with skull defection: A prospective randomized controlled study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003743
Enrollment
Unknown
Registered
2013-10-12
Start date
2014-02-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Epilepsy

Interventions

Two groups:levetiracetam prophylaxis vs without levetiracetam prophylaxis

Sponsors

The First Affiliated Hospital of PLA General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Subjects with 16-60 years old; 2. Subjects without seizure history before cranioplasty; 3. Subjects had no neurosurgical operation but the decompressive cranioectomy before cranioplasty; 4. Subjects whose score of Kamofsky Scale >=70; 5. Subjects with single skull defection; 6. Subjects who underwent cranioplasty with titanium meshes; 7. Subjects who are able to follow the investigational study procedures and who/whose family members are willing to give written consent for the study.

Exclusion criteria

Exclusion criteria: 1. Subjects with hydrocephalus who underwent vertriculperitoneal shunt at the same time with cranioplasty; 2. Subjects present intracranial hematoma or infection after cranioplasty; 3. Subjects with family epilepsy history.

Countries

China

Contacts

Public ContactShuli Liang

The First Affiliated Hospital of PLA General Hospital

liangsl_304@sina.com+86 13439390206

Outcome results

None listed

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