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To compare two different types of fluid in terms of their effect on the difference between the carbon dioxide level in central venous and arterial blood in patients undergoing neurosurgery

Evaluation of crystalloid vs colloid on CO2 gap in neurosurgical patients - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/12/060550
Enrollment
44
Registered
2023-12-20
Start date
Unknown
Completion date
Unknown
Last updated
2025-02-03

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Plasmalyte-crystalloid: Informed /written consent to participate in the study will be taken from the patient/relative.The patient will be fasting 6hrs for solids and 2 hrs for clear flu

Sponsors

Pt BD Sharma University of health sciences,PGIMS,Rohtak
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: belonging to ASA grade I-II undergoing neurosurgical procedure under general anaesthesia with arterial and central line placement.

Exclusion criteria

Exclusion criteria: any history of- Cardiac illness, Chronic renal disease, Known allergy to any fluid used in the study, Diabetes mellitus, Coagulation disorder, Deranged liver function test, Pregnant female, Refusal to consent

Design outcomes

Primary

MeasureTime frame
To assess the variation on CO2 gap with colloids and crystalloids in neurosurgical patientsTimepoint: At the time of incision,2hrs after incisional the time of closure, after 30 mins in PACU/ICU

Secondary

MeasureTime frame
To observe the effect of fluid therapy on-variation in haemodynamic parameters( Heart rate,mean arterial pressure, diastolic pressure,Systolic blood pressure,Oxygen Saturation,urine output )Timepoint: baseline,1st hour,2nd hour,3rd hour,4th hour,5th hour,6th hour,7th hour,PACU/ICU;To assess correlation between CO2 gap and other tissue hypo perfusion markers- lactate and central venous oxygen saturationTimepoint: At the time of incision, 2hrs after incision, at the time of closure, after 30 mins in PACU/ICU

Countries

India

Contacts

Public ContactDr Smita Chettri

Pt B D Sharma post graduate institute of medical sciences

smita631@gmail.com8509535058

Outcome results

None listed

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