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
- 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
1.ASA I & II patients
2.Patients aged above 18years
3.Patients undergoing neurosurgery in supine position under general anaesthesia
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
Name Time Method 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
Name Time Method Pleth Variability Index and Pulse Pressure VariationTimepoint: Baseline, 1 min, 3 min, 5 mins and 10 mins after completion of infusion.
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.