Postoperative Complications Clinical Trial
— NETTUNOOfficial title:
Hyperlactacidemia in Major Abdominal Surgery: Role of Variation in the Monocarboxylate Receptors
The goal of this clinical trial is to identify those situations in which the increase of lactate levels is not clinically relevant since it is associated with altered genetic polymorphism of the genes involved in the membrane proteins acting as carriers for lactate (mainly monocarboxylate transporters, MCTs) patients undergoing major abdominal surgery. The main questions it aims to answer are: 1. Is there a relationship between the lactate levels in the immediate post-operative period and the presence of some lactate receptor polymorphisms? 2. Can hyperlactacidemia related to lactate receptor polymorphisms affect length of stay in the recovery room and/or in intensive care unit, postoperative hospital stay, postoperative complications? - Which are the risk factors for hyperlactacidemia in the immediate post-operative period in addition to the presence of lactate receptors polymorphisms? Participants will undergo pre-operative genomic assay testing.
Status | Not yet recruiting |
Enrollment | 109 |
Est. completion date | October 2025 |
Est. primary completion date | August 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Age = 18 years - Indication for elective major abdominal surgery Exclusion Criteria: - Age <18 years - Liver cirrhosis - Liver surgery - Intraoperative chemotherapy - Previous gastric bypass surgery (thiamine deficiency) - Severe cardiovascular/respiratory impairment - Mitochondrial diseases - Pheochromocytoma - Chronic renal failure = stage III - Refusal to sign the informed consent |
Country | Name | City | State |
---|---|---|---|
Italy | UOC Anestesia delle Chirurgie Generali e dei Trapianti, Fondazione Policlinico Universitario A. Gemelli IRCCS | Rome | Italy/Lazio |
Lead Sponsor | Collaborator |
---|---|
Fondazione Policlinico Universitario Agostino Gemelli IRCCS |
Italy,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Lactate levels | Lactate levels (mmol/L) in the patients carrying the T allele versus the A allele for MCT1 gene. | 3 hours after the end of surgery | |
Secondary | Polymorphisms of lactate receptors (presence of MCT4 and GPR8) | Prevalence of the lactate receptors MCT4 and GPR8 polymorphisms throughout the genetic analysis of a blood sample. | Minutes and an average of 30 minutes before the start of surgery | |
Secondary | Lactate clearance | Evaluation of the association between lactate clearance (lactate levels at the end of surgery - lactate levels at 3 hours after the end of surgery)x100/lactate levels at the end of surgery and the presence of lactate receptor polymorphisms (MCT4 and GPR8). | 3 hours after the end of surgery | |
Secondary | Lactate clearance | Evaluation of the association between lactate clearance (lactate levels at the end of surgery - lactate levels at 24 hours after the end of surgery)x100/lactate levels at the end of surgery and the presence of lactate receptor polymorphisms (MCT4 and GPR8). | 24 hours after the end of surgery | |
Secondary | Postoperative recovery | Length of stay in recovery room (RR) or in intensive care (ICU) | Hours (RR) or days (ICU) and average of three hours for RR and one day in ICU | |
Secondary | In-hospital stay | Hospital stay duration | Days until discharge, an average of 7 day | |
Secondary | Hyperlactacidemia | Analysis of potential risk factors for hyperlactacidemia (lactate levels >2.2 mmol/L) as well as the presence of lactate receptor polymorphisms including age (years), comorbidities, American Society of Anesthesiologists (ASA) physical status classification system, Body Mass Index (kg/m2), type and duration of surgery (hours), surgical approach (open, laparoscopic, robotic), total of liquids administered (ml), total diuresis (ml), blood losses (ml), intraoperative blood components transfusions (units), blood gas analyses parameters, number of hypotensive episodes during surgery (MAP<65 mmHg) requiring the administration of norepinephrine or its dosage increase. | 3 hours after the end of surgery |
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