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Fluid responsiveness in patients undergoing surgery for traumatic brain surgery using intraoperative ECHO placed through esophagus and cardiac output monitoring

Fluid responsiveness in traumatic brain injury patients during surgery estimated using transesophageal echocardiography and FloTrac cardiac output monitoring: A Prospective Observational Study.

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2022/02/039919
Enrollment
30
Registered
2022-02-01
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

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

Conditions

Health Condition 1: S069- Unspecified intracranial injury

Interventions

None listed

Sponsors

NATIONAL INSTITUITE OF MENTAL HEALTH AND NEUROSCIENCES
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: • Patients aged between 18 to 60 years. • Isolated moderate to severe TBI patients undergoing surgery. • Patients operated in the supine position

Exclusion criteria

Exclusion criteria: Previous history suggestive of upper gastrointestinal surgery,esophageal varices,strictures , gastric ulcer Previous history suggestive of cardiac arrythmias , heart disease Patients with faciomaxillary surgeries,oropharyngeal bleed, cervical spine injury Pregnant patients Refusal by patients relatives

Design outcomes

Primary

MeasureTime frame
To estimate fluid responsiveness in isolated TBI patients during surgery using SVCCI and SVV compared to fluid challenge with CI.Timepoint: 1.After induction of anesthesia. 2. After 5ml/kg bolus of crystalloid over 10 minutes. 3. After craniotomy. 4. At the end of surgery.—

Secondary

MeasureTime frame
1.To determine the correlation between dynamic parameters derived from TEE and FloTrac monitor. 2.To determine the neurological outcome of patients between fluid responders and non-responders. Timepoint: 1.After induction of anesthesia. 2.After 5ml/kg bolus of crystalloid over 10 minutes. 3.After craniotomy. 4.At the end of surgery. GOS at discharge and at 3 months over telephone—

Countries

India

Contacts

Public ContactAMRUTA NIRALE

NATIONAL INSTITUTE OF MENTAL HEALTH AND NEUROSCIENCES, BENGALURU

gops868@gmail.com9916469626

Outcome results

None listed

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