General Anesthesia Clinical Trial
Official title:
Evaluation of BNP Values in Major Vascular Surgery
Background and rationale of the study:
Patients undergoing non-cardiac major surgery show a perioperative cardiac risk and
postoperative complications, that can be stratified based on parameters linked to patient's
conditions and to surgery types.
An accurate identification of this risk could offer numerous advantages for these patients,
who's 30-day mortality is around 2%. The identification of the correct risk could lead to a
better pre- and postoperative management, that could guarantee a better surgery outcome and a
faster postoperative recovery.
To this day there is no perfect method to correctly estimate this risk. Various studies show
that high BNP levels are linked to cardiac events at 30 and 180 days. Further investigations
identify different groups, at low, intermediate and high risk, based on BNP levels.
BNP is released by ventricular myocytes in response to a wall distress, due to an increased
volume, pressure or myocardial ischemia.
So BNP plasma levels could be used as a prognostic and diagnostic marker, improving the
cardiac risk stratification in patients undergoing surgery and a much more precise
management.
This study is determined to do an evaluation of the correlations between pre- and
postoperative BNP levels and the incidence of cardiac events in patients undergoing major
vascular surgery.
Patient's informed consent signature for adhesion at the study will be initially requested.
With their acceptance, parameters will be recorded anonymously in the Case Report Form,
identified by their initials and a numeric code, until hospital discharge.
The parameters analyzed will be related to:
- preoperative evaluation: anamnesis, health general conditions, METs, preoperative
monitoring, in particularly BNP basal levels;
- intraoperative evaluation: intraoperative monitoring;
- postoperative evaluation: BNP and cTnI levels at 24 and 48 hours, and about pulmonary,
cardiovascular, neurological and surgical postoperative complications, based on the
medical record.
The data will be transferred on Excel worksheet, utilized for descriptive analysis related at
every variable.
;
| Status | Clinical Trial | Phase | |
|---|---|---|---|
| Completed |
NCT04577430 -
Effects of Dexmedetomidine on Cardiac Electrophysiology in Patients Under General Anesthesia During Perioperative Period
|
N/A | |
| Completed |
NCT03708692 -
Menstrual Cycle Phases on Recovery and Cognitive Function
|
||
| Recruiting |
NCT03422315 -
Population Pharmacokinetics and Clinical Individual Dosage Regimen of Propofoll Injection
|
N/A | |
| Completed |
NCT02771067 -
The Utility of Pulse Pressure Variation to Predict the Fluid Responsiveness During Pneumoperitoneum and Reverse-Trendelenburg Position
|
N/A | |
| Completed |
NCT05063461 -
Evaluation of the Analgesia Nociception Index With Varying Remifentanil Concentrations Under Sevoflurane
|
N/A | |
| Completed |
NCT03294226 -
Comparison of AuraGain With I-gel for Pediatric Patients
|
N/A | |
| Not yet recruiting |
NCT03643029 -
The Accuracy of the Performance and Placement Test for Predicting Supraglottic Airway Device (SAD) Position in the Hypopharynx as Confirmed With Video Laryngoscopy
|
N/A | |
| Completed |
NCT01945411 -
Assessment of Facial Measurements, the Length of Mouth Corner-mandible Angle and Incisors-mandible Angle, for Determining the Proper Sizes of Oropharyngeal Airway
|
N/A | |
| Completed |
NCT01705743 -
Minimum Alveolar Concentration of Sevoflurane With Nitrous Oxide Inducing Isoelectric EEG
|
Phase 4 | |
| Not yet recruiting |
NCT01678066 -
A Prospective Study to Bilaterally Compare a Non-Invasive Cardiac Output Monitor
|
N/A | |
| Completed |
NCT00972491 -
The Optimal Time to Put Laryngeal Mask Airway in the Mouth Under General Anesthesia
|
N/A | |
| Completed |
NCT01096212 -
Efficacy and Safety of Sevofran in Patients Scheduled for Elective Surgery Under General Anesthesia
|
Phase 4 | |
| Completed |
NCT00741507 -
Unhealthy Alcohol Drinking and Anesthetic Requirement in Women
|
N/A | |
| Completed |
NCT00599066 -
Intraoperative M-Entropy Measurements
|
N/A | |
| Completed |
NCT00532402 -
Continuous and Discontinuous Determination of Propofol Concentration in Breathing Gas
|
N/A | |
| Completed |
NCT00468494 -
Can Blood Glucose Levels During the Perioperative Period Identify a Population at Risk for Hyperglycemia?
|
N/A | |
| Recruiting |
NCT00492453 -
Spinal Versus General Anesthesia for Laparoscopic Cholecystectomy
|
N/A | |
| Recruiting |
NCT03745079 -
Correlation Between Core Temperature and Skin Temperature Measured by 3M SpotOn
|
||
| Completed |
NCT04094376 -
Comparison of Morning Operation and Evening Operation on Postoperative Sleep Quality and Pain Under General Anesthesia
|
N/A | |
| Enrolling by invitation |
NCT03672734 -
Volume and pH of Gastric Contents in Patients Undergoing Gynecologic Laparoscopic Surgery During Emergence From General Anesthesia
|