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Not yet recruiting Not applicable NCT07310043

Creatine and Perioperative Brain Health

No applicable phase (e.g. observational)
Conditions: Neurocognitive Disorders Postoperative Delirium

Sponsor: Massachusetts General Hospital

trial.available_in: БГ
Overview
The goal of this study is to understand the effects of oral creatine supplementation in the perioperative period. Creatine is commonly used to enhance athletic performance, but it can also have positive effects on the brain. Since surgery can lead to alterations in thinking, memory, and attention patterns in some patients, we will assess whether creatine can be protective against these changes in older adults undergoing surgery.
Description
Surgical interventions, while often necessary, are associated with substantial postoperative morbidity, particularly among older adults. Perioperative neurocognitive disorders (PND), characterized by changes in memory patterns in the perioperative period and are among the most common surgical complications in aging populations. Beyond their considerable economic burden, estimated to exceed $30 billion annually, PND impose profound immediate consequences for patients and caregivers and is associated with long-term adverse outcomes, including an increased risk of dementia. Despite their high prevalence and clinical impact, effective, scalable, and easily implementable preventive strategies for PND remain limited. Creatine plays a critical role in supporting the brain's high metabolic demands, and its homeostasis may be disrupted during periods of physiological stress such as anesthesia and surgery. Creatine supplementation has demonstrated neuroprotective effects in other high-stress conditions. However, its potential to mitigate perioperative cognitive vulnerability has not been previously investigated. This study will evaluate creatine supplementation as a novel protective strategy to reduce the risk of PND in older adults undergoing surgery.
Who can participate
Inclusion Criteria: * Patients scheduled for elective surgery under general anesthesia Exclusion Criteria: * History of creatine deficiency disorders * Severe neurologic or psychiatric diseases * History of stroke or head trauma * Obesity (BMI ≥ 30 kg.m-²), kidney or liver disease
Interventions
Creatine monohydrate
DIETARY_SUPPLEMENT
Locations

Location information is not available.

Technical details
Status
Not yet recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
60 Years
Maximum age
75 Years
Healthy volunteers
No
Start date
01.07.2026
Completion date
30.06.2028
Registry ID
NCT07310043
Source
clinicaltrials.gov
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