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se of monitor to transfuse blood in patients undergoing spine surgeries. A comparison with laboratory tests.

Phase 3
Conditions
Health Condition 1: G988- Other disorders of nervous system
Registration Number
CTRI/2019/05/019084
Lead Sponsor
AIIMS New Delhi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

undergoing spine instrumentation surgery under general anesthesia.

Exclusion Criteria

patients with a history of previous intracranial surgery, any history of peripheral vascular disease, hemoglobinopathy, sickle cell disease or non-consenting patients and PI <1.4

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.We aimed to compare invasive hemoglobin (Hb) values versus non-invasive Hb values at the trigger point for blood transfusion [9 gm%]. <br/ ><br> <br/ ><br>Timepoint: The non-invasive hemoglobin monitoring [SpHb®] probe will be applied to the patient immediately after the induction of anesthesia, but before the start of surgery and approximately every 30 minutes thereafter till end of surgery. <br/ ><br>Intraoperatively at any time point if the non-invasive Hb value reaches the trigger point for blood transfusion i.e 9 gm%, arterial blood sample will be collected for Hb estimation using arterial blood gas (ABG) machine (aHb). <br/ ><br> <br/ ><br>
Secondary Outcome Measures
NameTimeMethod
2.We will also assess the cerebral oxygenation at the above time point using near infrared spectroscopy [NIRS]Timepoint: Intraoperatively at any time point if the non-invasive Hb value reaches the trigger point for blood transfusion i.e 9 gm%, arterial blood sample will be collected for Hb estimation using arterial blood gas (ABG) machine (aHb). Simultaneously, the cerebral oxygenation value will be recorded at same time point.
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