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Clinical Trials/NCT05239286
NCT05239286
Completed
Not Applicable

Comparison Between Conventional Fluid Management and Plethysmographic Variability Index Based Goal Directed Fluid Management in Patients Undergoing Spine Surgeries in Prone Position; A Randomized Control Trial.

Cairo University1 site in 1 country66 target enrollmentJanuary 24, 2022

Overview

Phase
Not Applicable
Intervention
General anaesthesia
Conditions
Fluid Management During Elective Spine Surgeries
Sponsor
Cairo University
Enrollment
66
Locations
1
Primary Endpoint
The total intraoperative crystalloid consumption
Status
Completed
Last Updated
3 years ago

Overview

Brief Summary

Plethysmographic variability index is a dynamic method for evaluation of volume status which depends on estimation of respiratory variations in pulse oximeter waveform amplitude. The PVI has been studied in various patient populations and clinical settings, and has been shown to reliably predict fluid responsiveness and guide fluid resuscitation.

conventional fluid management. Fluid replacement is managed according to clinical assessment, heart rate, arterial blood pressure and central venous pressure monitoring. However, clinical studies indicate that changes in ABP cannot be used for the monitoring of stroke volume and cardiac output. Another method is the goal-directed fluid management and it is based on individualized fluid management using static and dynamic parameters.

Detailed Description

This study aims to compare the conventional fluid managment and Plethysmographic Variability index based during elective spine surgeries in prone position. the study hypothesize is: plethysmographic variability index (PVI) based fluid management is more accurate than conventional method in preventing hypovolemia ana hypotension associated with prone position. The patients will be randomly assigned into two equal groups using computer-generated random numbers with closed envelop, each of which will include 33 patients. Group conventional: (n=33) patients are in the conventional fluid management group. Group PVI: (n=33) patients are in the PVI-based goal-directed fluid management group.

Registry
clinicaltrials.gov
Start Date
January 24, 2022
End Date
September 30, 2022
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Bassant M. Abdelhamid

Assisstant Professor

Cairo University

Eligibility Criteria

Inclusion Criteria

  • • Adult patients (18-65 years)
  • Patients scheduled for elective lumbar spine surgeries (e.g.: Lumbar fixation and simple discectomy) under general anaesthesia in prone position.

Exclusion Criteria

  • • Operations which will last for less than 15 minutes. (e.g.: plate and screw adjustment or incomplete terminated surgery)
  • Patients with cardiac morbidities e.g. history of unstable angina, impaired contractility with ejection fraction \< 40%, wall motional abnormalities or tight valvular lesions detected by echocardiography, previous cardiac operations or cardiac catherization with stent.
  • Patients with heart block and arrhythmia (atrial fibrillation and frequent ventricular or supraventricular premature beat).
  • Patient with decompensated respiratory disease (poor functional capacity, generalized wheezes, peripheral O2 saturation \< 90% on room air).
  • Patients with peripheral vascular disease or long-standing DM affecting PVI readings.
  • Complicated surgeries (huge spine tumors, intraoperative vascular or neurological complications and prolonged durations more than 5 hours) or surgeries with massive blood loss (4 units of packed RBCs in 1 hour or replacement of 50% of total blood volume within 3 hours )
  • Pregnancy.

Arms & Interventions

Group conventional

Intervention: General anaesthesia

Group conventional

Intervention: Conventional fluid managment

Group PVI

Intervention: General anaesthesia

Group PVI

Intervention: PVI dependant goal directed fluid therapy

Outcomes

Primary Outcomes

The total intraoperative crystalloid consumption

Time Frame: 3 hours

the total volume of infused crystalloids intraoperatively.

Secondary Outcomes

  • mean arterial blood pressure(3 hours)
  • Blood lactate level(3 hours)
  • Plethysmographic variability index(3 hours)
  • perfusion index(3 hours)
  • Heart rate(3 hours)
  • Total amount of intraoperative urine output(3 hours)
  • The need and the amount of intraoperative blood transfusion(3 hours)

Study Sites (1)

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