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Ultrasonographic assessment to maintain optimal cerebral perfusion and titrate norepinephrine in patients with septic shock

Use of trans cranial doppler to titrate norepinephrine for optimal cerebral perfusion in septic shock - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/076762
Enrollment
80
Registered
2024-11-13
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: B998- Other infectious disease

Interventions

Intervention1: Norepinephrine: Titration of Norepinephrine dose based on pulsatility index on Transcranial Doppler Control Intervention1: Pulsatility index on Transcranial Doppler: Titration of Norepi

Sponsors

Dayanand Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patient admitted to Intensive Care Units with early septic shock defined as within 6 hours of start of norepinephrine infusion

Exclusion criteria

Exclusion criteria: Age less than eighteen years Negative consent for participation in study Known cerebrovascular lesions and events like ischemic or hemorrhagic stroke History of head injury or other causes of increased ICP Known cerebral infection Known severe Carotid artery stenosis Other causes leading to encephalopathy

Design outcomes

Primary

MeasureTime frame
To titrate norepinephrine infusion using Trans cranial Doppler variable, pulsatility index ,to maintain optimal cerebral perfusion in septic shock and to assess the neurological outcome when TCD is used to titrate the norepinephrine infusion.Timepoint: Day 0, Day 1, Day 3 and after inotropes are stopped

Secondary

MeasureTime frame
? Assessment of change in neurological status in patients with septic shock when PI is used to titrate norepinephrine dose. ? To assess the impact of TCD derived titration of nor epinephrine on length of ICU stay, ventilator free days, & outcome. Timepoint: Day 0, Day 1, Day 3 & when inotropes are stopped

Countries

India

Contacts

Public ContactJASMINE KAUR KOCHHAR

Dayanand Medical College and Hospital, Ludhiana

parshotamg@yahoo.com9814176565

Outcome results

None listed

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