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A study done to evaluate the usefulness of changes in a non- invasive parameter called End Tidal Carbon Dioxide after giving fluid infusion to neurosurgery patients to predict whether they will respond with an increase in cardiac output

Not Applicable
Conditions
Health Condition 1: G968- Other specified disorders of central nervous system
Registration Number
CTRI/2024/01/061105
Lead Sponsor
Dr. Anjali R Hegde
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

1.ASA I & II patients

2.Patients aged above 18years

3.Patients undergoing neurosurgery in supine position under general anaesthesia

Exclusion Criteria

1. Patients with cardiac arrhythmias, valvular heart diseases or left or right heart failure

2. Patients with chronic obstructive pulmonary disease with a MMRC Dyspnea Scale 3 or more

3. Patients with intrathoracic lesions

4. Pregnant women

5. Patients on vasoactive drugs

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in End tidal carbon dioxide after volume expansion to predict fluid responsiveness defined as fall in Pleth Variability Index to less than 14 percent and increase in SBP by 10 mm Hg or moreTimepoint: Baseline, 1 min, 3 min, 5 mins and 10 mins after completion of infusion.
Secondary Outcome Measures
NameTimeMethod
Pleth Variability Index and Pulse Pressure VariationTimepoint: Baseline, 1 min, 3 min, 5 mins and 10 mins after completion of infusion.
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