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Comparison of anaesthetic agents on intravascular layer in patients undergoing surgery for traumatic brain injury

Comparison of sevoflurane and propofol on vascular endothelial glycocalyx in patients undergoing surgery for traumatic brain injury - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/10/075202
Enrollment
50
Registered
2024-10-14
Start date
Unknown
Completion date
Unknown
Last updated
2026-03-30

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

Conditions

Health Condition 1: G939- Disorder of brain, unspecified

Interventions

Intervention1: Sevoflurane: Sevoflurane group: anaesthesia will be maintained with fentanyl 1 µg/kg/h, rocuronium 0.1 mg /kg/h, and sevoflurane (0.8-1 MAC) titrated to a BIS between 40 and 60. Contro

Sponsors

AIIMS NEW DELHI
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients aged between 18 and 60, of either gender, belonging to ASA physical status Iâ??II undergoing emergency decompressive craniotomy for traumatic brain injury requiring general anaesthesia.

Exclusion criteria

Exclusion criteria: Patients with mild moderate head injury Patients with SBP less then 90 mmHg Previous history of heart disease or surgery. Hemodynamic instability requiring medical or mechanical attention Severe hepatic and renal insufficiency, and Severe chronic obstructive pulmonary disease

Design outcomes

Primary

MeasureTime frame
To compare the syndecan-1 and Heparan sulfate (HS) levels between sevoflurane and propofol-based anesthesia in moderateâ??toâ??severe Traumatic brain injury (TBI) patients undergoing decompressive craniectomyTimepoint: Starting point-prior to induction of anaesthesia as baseline values, intraoperatively at every 10 min interval till the end of surgery End Point-12 h after completion of surgery.

Secondary

MeasureTime frame
To compare the effect of the degree of endotheliopathy on the Intensive care unit (ICU) and hospital stay among patients with TBI between sevoflurane and propofol-based anesthesiaTimepoint: Starting point-prior to induction of anaesthesia as baseline values, intraoperatively at every 10 min interval till the end of surgery End Point-12 h after completion of surgery

Countries

India

Contacts

Public ContactDr Niraj Kumar

All India Institute of Medical Sciences, New Delhi

drnirajaiims@gmail.com09013770806

Outcome results

None listed

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