The overall goal of this study is to evaluate the feasibility of perioperative oral creatine supplementation and to explore its effects on cognitive function and physiological responses to surgery in older adults. Creatine is commonly used to enhance athletic performance, but it can also have positive effects on the brain. Since surgery can alter thinking, memory, and attention patterns in some patients, we will assess whether creatine affects these changes in older adults undergoing surgery.
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, are among the most common surgical complications in aging populations. Beyond their considerable economic burden, estimated to exceed $30 billion annually, PND imposes 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 been demonstrated to be neuroprotective in high-stress conditions. However, the potential effects of creatine during perioperative cognitive vulnerability have not been previously investigated. This study will evaluate the feasibility of creatine supplementation in the perioperative period and explore its effects on cognitive function and physiological responses to surgery in older adults.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Enrollment
120
Participants will receive creatine supplementation before surgery
Participants in the placebo group will receive an identical placebo before surgery
Preoperative cognitive function assessed with the Montreal Cognitive Assessment (MoCA)
The MoCA is a validated tool to assess cognitive function. Scores range from 0-30, with higher scores representing better cognitive function
Time frame: Within three weeks before surgery
Postoperative cognitive function assessed with the Montreal Cognitive Assessment (MoCA)
The MoCA is a validated tool to assess cognitive function. Scores range from 0-30, with higher scores representing better cognitive function
Time frame: Within one month after surgery
Postoperative cognitive function assessed with the Montreal Cognitive Assessment (MoCA)
The MoCA is a validated tool to assess cognitive function. Scores range from 0-30, with higher scores representing better cognitive function
Time frame: Within three months after surgery
Postoperative delirium assessed with the Confusion Assessment Method (CAM)
The CAM is a validated tool to detect postoperative delirium
Time frame: Up to 7 days after surgery
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