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Pre surgical volume status determination in patients of subarachnoid haemorrhage determination

To determine the incidence of hypovolemia in preoperative period and its correlation with incidence hypotension in patients with aneurysmal subarachnoid haemorrhage

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2018/07/015135
Enrollment
100
Registered
2018-07-31
Start date
Unknown
Completion date
Unknown
Last updated
2023-05-29

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

Conditions

Health Condition 1: null- Patients with Subarachnoid haemorrhage posted for craniotomy and clipping will be enrolled in the study

Interventions

None listed

Sponsors

PGIMER
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients with Subarachnoid haemorrhage posted for craniotomy and clipping will be enrolled in the study

Exclusion criteria

Exclusion criteria: Extremes of ages 65 years End organ failure/severe end organ damage Pregnancy Stunned myocardium Patients with known cardiac illness, severe arrhythmias and preoperative moderate/severe left ventricular dysfunction will not be assessed for induction hypotension

Design outcomes

Primary

MeasureTime frame
â??The primary objective of the study is to assess the incidence of hypovolemia in patients with Subarachnoid Haemorrahge using Inferior Vena Cava collapsibility index and Echocardiographic parameters.Timepoint: Before half an hour of surgery

Secondary

MeasureTime frame
Association of pre-operative Hypovolemia with induction hypotension.Timepoint: Within 10 minutes of induction;Incidence of Hypotension after induction with propofol.Timepoint: Within first 10minutes of induction

Countries

India

Contacts

Public ContactDasari Gurucharan

Junior resident, department of Anaesthesia and intensive care

dasaribunny@yahoo.com

Outcome results

None listed

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