Clinical trial

Analyzing the Neuroprotective Effect of Dexmedetomidine in Terms of Preserving Brain Functional Connectivity in Elderly Patients After Major Surgery

Name
200618004
Description
Older patients are more prone to adverse cognitive outcomes such as postoperative delirium (POD) and postoperative cognitive dysfunction (POCD). Both conditions are associated with an increased risk of death, functional decline, and health care costs. The presence of pro-inflammatory cytokines in the central nervous system has detrimental effects on the regulation of neurotransmitter signaling in different areas of the brain, especially the hippocampus, ultimately resulting in neuronal dysfunction and cognitive decline. Neuroimaging studies have provided important information on the structural and functional networks involved in the pathogenesis of POD and POCD. Strong evidence has shown a decrease in the integrity of the default mode network (DMN), along a continuum from normal aging to mild cognitive impairment and Alzheimer's disease. Dexmedetomidine is a highly selective alpha-2 adrenergic agonist with sedative and analgesic properties but minimal respiratory effects. Several studies have shown that dexmedetomidine reduces serum pro-inflammatory cytokines and POCD. The expected results are to analyze the change in the integrity of the DMN from the preoperative period to the first weeks after discharge given by the two anesthetic strategies (SEVO vs SEVODEX). In addition, it seeks to evaluate (1) Changes in the integrity of the DMN at 3 months. (2) Modulation of structural changes in white matter integrity as measured by DTI. (3) Patient performance in specific cognitive function tests and serum inflammation biomarkers between the pre- and postoperative period. For the analysis, the Generalized Linear Model (GLM) will be used, in which the integrity of the DMN is the dependent variable. As predictors will use the anesthetic groups (SEVO and SEVODEX) and the measurement time (preoperative, 1 to 3 weeks after discharge and 3 months later as levels). With this work we aim to provide a mechanistic explanation of the observed neuroprotective effects of dexmedetomidine in anesthesia protocols for elderly patients. Furthermore, this work will possibly promote functional connectivity as a possible clinical biomarker of cognitive impairment in this vulnerable population.
Trial arms
Trial start
2021-11-16
Estimated PCD
2024-06-15
Trial end
2024-09-01
Status
Recruiting
Treatment
Dexmedetomidine
These participants will receive intraoperative dexmedetomidine.
Arms:
SEVODEX Group
Other names:
Sevoflorane
Placebo
These participants will not receive intraoperative dexmedetomidine.
Arms:
SEVO Group
Size
50
Primary endpoint
Reduction of the alteration of the NDM due to the effect of dexmedetomidine associated with sevoflouran in elderly patients under general anesthesia
f-MRI before surgery (t0), f-MRI two to four weeks post discharge (t1), Three months post discharge (t2)
Eligibility criteria
Inclusion Criteria: * ASA I, II or III. * Body mass index (BMI) \<35 kg/m2. * Scheduled at least 6 days prior to surgery to allow adequate time for the baseline assessment. * Planned admission to the hospital for at least 2 days. Exclusion Criteria: * Active delirium diagnosed with the Confusion Assessment Method (CAM). * Mild cognitive impairment or dementia diagnosed with the Spanish-language version of the Montreal Cognitive Assessment MoCA-S1-2 score (score \<20 points). * In case the patient cannot answer the MoCA test, the instrument AD8-Ch will be applied. * Hospitalization within 3 months prior to enrollment to minimize risk of recent delirium history. * Severely frail condition defined with the Clinical Frailty Scale (CFS ≥7). * Inability to perform cognitive tests due to legal blindness or severe deafness * History of schizophrenia or psychosis. * Harmful alcohol use or alcohol dependence (AUDIT score ≥16 considering the standard drink equivalent determined by MINSAL). * History of benzodiazepines or marihuana consumption (more than 3 days per week). * Unable to pass assessment for capacity to provide informed consent. * Claustrophobia.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['NA'], 'designInfo': {'allocation': 'RANDOMIZED', 'interventionModel': 'PARALLEL', 'interventionModelDescription': 'Participants will be randomly assigned to any of the groups: Control Group and DEX Group', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'DOUBLE', 'maskingDescription': 'Each participant will be assigned an identifier that the research team will use from enrollment to follow-up.', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER']}}, 'enrollmentInfo': {'count': 50, 'type': 'ESTIMATED'}}
Updated at
2024-03-28

1 organization

1 product

1 drug

3 indications

Indication
Anesthesia
Indication
Dexmedetomidine
Indication
Aging