To hear about similar clinical trials, please enter your email below
Trial Title:
Effects of Two Different Goals of Fluid Management in Patients Undergoing Supratentorial Tumour Resection
NCT ID:
NCT05561894
Condition:
Supratentorial Brain Tumor
Conditions: Official terms:
Brain Neoplasms
Study type:
Interventional
Study phase:
N/A
Overall status:
Unknown status
Study design:
Allocation:
Randomized
Intervention model:
Parallel Assignment
Primary purpose:
Supportive Care
Masking:
Double (Participant, Outcomes Assessor)
Intervention:
Intervention type:
Other
Intervention name:
pulse pressure variation index guided fluid therapy
Description:
maintainence intraoperative fluid therapy (ringer's acetate) will be given guided by
either two goals of pulse pressure variation index, either >12% or >16%
Arm group label:
A (control)
Arm group label:
B
Summary:
Neurosurgical operations are characterised by major fluid shift, frequent use of
diuretics, and prolonged operative time. The role of fluid therapy in these patients is
very critical; hypovolemia might decrease cerebral perfusion; while, fluid over-infusion
might swell the brain (1-3). Thus, fluid management in these procedures complex and
challenging. Evidence on the optimum protocol for intraoperative fluid management in
neurosurgical patients is still lacking. Adequate intracranial volume management is
considered a key factor that would overcome the tumour bulk and the surrounding vasogenic
oedema facilitating surgical access . Thus, a relaxed brain is one of the targets of
intraoperative fluid management during craniotomy. The slack brain would allow proper
surgical retraction and consequently, reduces brain retractor ischemia. Brain relaxation
scale (BRS) had shown a good correlation with intracranial pressure thus, an increasing
interest was paid to BRS as a simple surrogate for intracranial pressure (4-8).
Goal-directed hemodynamic therapy (GDT) in the operating room is a term used to describe
the use of defined hemodynamic targets to guide intravenous fluid and inotropic therapy.
Pulse pressure variation (PPV) is one of the robust dynamic indices of fluid
responsiveness which is based on heart-lung interactions (9-12). GDT had been frequently
investigated in the operating room in high-risk patients especially in major surgery.
However, the impact of GDT on patient outcomes, especially BRS, is not well evaluated in
brain surgery (12-15). In this study, we evaluated PPV-guided fluid management compared
to standard fluid management in patients undergoing supratentorial mass excision. We
hypothesised that in these procedures, GDT might restrict intraoperative fluid volume,
improve brain relaxation, and provide stable patient hemodynamics.
Detailed description:
Anesthetic management:
Peripheral i.v line will be inserted and 2-3 mg midazolam and 2 gm magnesium are given. A
pre-induction radial arterial line is inserted with the aid of infiltration of 2 ml
lidocaine 2%. Invasive arterial blood pressure monitoring is started and pulse oximetry,
5-leads ECG, and NIBP are attached to the patient and mindray ipm-12 monitor is used.
Anesthetic induction started with propofol 1-2 mg/kg, lidocaine 1 mg/kg, cis-atracurium
0.2 mg/kg and fentanyl 1-2 microgram/kg. Intubation is done with cuffed endotracheal tube
and tidal volume and respiratory rate are set to achieve end-tidal Co2 of 30-28 mmHg.
Esophageal temperature probe and urinary catheter are put in place. Patients then will
receive maintenance of anesthesia with isoflurane < 1 MAC, propofol 10-60
microgram/kg/min, dexmedetomidine loading 1 microgram/kg bolus in 10 minutes followed by
0.2-1 microgram/kg/hour and cis-atracurium 2-3 microgram/kg/minute. Patients will receive
mannitol 20% 0.5-1 gm/kg and dexamethasone 8mg and paracetamol 1gm near the end of
surgery. Patients will receive their fasting requirements of normal saline in the first 3
hours of surgery. Maintenance fluid used will be ringer acetate and will be given
according to pulse pressure variation index (PPVI) that is derived from pulse contour
analysis of invasive arterial blood pressure waveform. Patients are then divided into two
groups of two different targets of PPVI. Group A will be given ringer acetate when PPVI
is > 12% and group B will be given ringer acetate when PPVI is > 16%.
If hypotension occurred without change in PPVI targets, it will be treated with 10 mg
ephedrine. Arterial blood gas samples will be collected at induction and at the end of
surgery. After removal of cranial fixation pins, anesthesia is discontinued and reversal
of muscle relaxant is done with atropine 0.5 mg and neostigmine 0.05 mg/kg then
extubation is done and patient is transferred to the ICU.
Criteria for eligibility:
Criteria:
Inclusion Criteria:
ASA 1,2 patients undergoing supratentorial tumour resection Age > 18 years Supine
position
Exclusion Criteria:
- ASA 3,4 patients and patients with GCS < 13
- Any other position rather than supine position
- AF or any significant arrhythmia
- Severe bradycardia that leads to low HR/RR ratio
- Severe tricuspid regurgitation or severe right ventricular dysfunction
- Patients with severe restrictive lung pathology and needing low tidal volumes
Gender:
All
Minimum age:
18 Years
Maximum age:
N/A
Healthy volunteers:
No
Locations:
Facility:
Name:
Faculty of medicine, Assiut university
Address:
City:
Assiut
Zip:
71111
Country:
Egypt
Contact:
Last name:
Ibraheem Abdelmageed
Phone:
+201142429670
Email:
dr.ibraheemembaby@gmail.com
Start date:
December 15, 2022
Completion date:
October 20, 2023
Lead sponsor:
Agency:
Assiut University
Agency class:
Other
Source:
Assiut University
Record processing date:
ClinicalTrials.gov processed this data on November 12, 2024
Source: ClinicalTrials.gov page:
https://clinicaltrials.gov/ct2/show/NCT05561894