Electrocorticographic Monitoring In Head Injuries

Intraoperative Electrocorticographic Monitoring for predicting Posttraumatic Seizures and Prognosticating Head Injury Patients - A Prospective Observational Study

Status

Recruiting

Phases

Phase 3

Study type

Observational

Source

CTRI

Registry ID

CTRI/2019/05/019425

Enrollment

110

Registered

2019-05-29

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

Health Condition 1: S063- Focal traumatic brain injury

Interventions

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of moderate and severe head injury who are going to be operated for evacuation of hematoma or decompression surgery. 2. Patients of all age groups

Exclusion criteria

Exclusion criteria: 1. Patients with infected wound. 2. Patients with metabolic abnormality, cardiac abnormality, renal failure and respiratory disease. 3. Patients with associated trauma of other body regions. 4. Patients or their relatives denying taking part in the study.

Design outcomes

Primary

Measure	Time frame
To evaluate the development of posttraumatic seizures in severe head injury in patients with normal (Group A) and abnormal (Group B) intraoperative electrocorticography.Timepoint: Baseline, 7 days, 30 days, 6 months	—

Secondary

Measure	Time frame
To evaluate the extended Glasgow outcome scale, modified Rankin scale, and quality of life in severe head injury in patients with normal (Group A) and abnormal (Group B) intraoperative electrocorticography.Timepoint: 7 days, 30 days, 6 months	—

Countries

India

Contacts

Public ContactJitin Bajaj

NSCB Govt. Medical College, Jabalpur, MP, India

bajaj.jitin@gmail.com8696982911

Outcome results