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An observational study undertaken to study effect of change in blood pressure, blood CO2, blood glucose, body temperature, heart rate during operative procedures in traumatic brain injury patients undergoing surgeries for extracranial injury and its correlation with post operative outcome.

Evaluation of the incidence intraoperative secondary brain insults in extra-cranial surgeries in traumatic brain injury and their correlation with post-operative neurological outcome—A prospective observational study. - NIL

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/06/069549
Enrollment
55
Registered
2024-06-26
Start date
Unknown
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

Health Condition 1: S099- Unspecified injury of face and head

Interventions

Intervention1: NIL: NIL

Sponsors

Lokmanya Tilak Municipal Medical College and General Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients having traumatic brain injury,as confirmed on CT Brain, undergoing extracranial surgery within 72 hours of admission. 2. Age more than 18 years of age. 3. Patients with Systolic blood pressure more than or equal to 90 mmHg with or without ionotropic supports 4.Patient with Glasgow coma score more than or equal to 13 i.e, moderate to severe traumatic brain injuries. 5.Patients with any other comorbidities like chronic obstructive pulmonary disease, ischaemic heart disease, chronic kidney disease, etc.

Exclusion criteria

Exclusion criteria: 1.Patients less than 18yrs. 2.Patients/Relatives not willing to give consent. 3.Patients undergoing craniotomy before extracranial surgery. 4.TBI patients undergoing extracranial surgery beyond 72 hours.

Design outcomes

Primary

MeasureTime frame
Changes in CT Brain of patient post operatively.Timepoint: 24 hours—

Secondary

MeasureTime frame
Increase in ventilatory settings as compared to preoperative settingsTimepoint: 24 hours;Requirement of ionotropic supportTimepoint: 24 hours—

Countries

India

Contacts

Public ContactDr Shalaka Nellore

Lokmanya Tilak Municpal Medical College and General Hospital,Sion Mumbai

shalakagandhi@gmail.com9820625058

Outcome results

None listed

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