Effect of Micronized Creatine Monohydrate on Muscle Mass, Strength and Performance in Older Adults Submitted to Total Knee Arthroplasty
Launched by CONSORCI SANITARI DEL MARESME · Apr 11, 2025
Trial Information
Current as of June 26, 2025
Not yet recruiting
Keywords
ClinConnect Summary
This clinical trial is studying the effects of a supplement called micronized creatine monohydrate on older adults who have had total knee replacement surgery. The goal is to see if taking creatine can help improve muscle mass, strength, and overall physical performance during recovery. Participants in the study will take creatine daily for 12 weeks, starting with a higher dose for the first week and then a lower dose for the rest of the trial.
To be eligible, participants must be at least 65 years old, have recently undergone their first knee replacement surgery, and be involved in a standard rehabilitation program. However, those with certain health conditions, such as severe kidney or liver issues, specific neuromuscular diseases, or significant cognitive impairment, will not be included. Throughout the trial, researchers will measure changes in muscle strength and function at the beginning, and again at 3 and 6 months after starting the supplement. This study aims to provide valuable information about how creatine can support recovery in older adults after knee surgery.
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • Persons 65 years of age or older who have been operated on for the first time for total knee arthroplasty,
- • who are undergoing an outpatient rehabilitation program according to standard clinical practice,
- • who sign the informed consent form.
- Exclusion Criteria:
- • Chronic renal disease at stage G3b or higher or glomerular filtration rate \<30 ml/min/1.73m2.
- • Hepatic insufficiency, cirrhosis.
- • Neuromuscular and neurodegenerative diseases (amyotrophic lateral sclerosis, multiple sclerosis, muscular dystrophy, myasthenia gravis, Parkinson's disease, etc.).
- • Severe or very severe chronic obstructive pulmonary disease (COPD) (GOLD III-IV).
- • Moderate or severe chronic heart failure (NYHA 3-4).
- • Central sensitivity syndrome (fibromyalgia and chronic fatigue syndrome).
- • Moderate or severe cognitive impairment (GDS≥4).
- • Moderate-severe dependence for basic activities of daily living (preintervention Barthel index \<60 points).
- • Hemiparesis, amputation or malformation of any limb.
- • Consumption of creatine monohydrate supplements in the last 6 months.
About Consorci Sanitari Del Maresme
Consorci Sanitari del Maresme is a prominent healthcare consortium located in the Maresme region of Catalonia, Spain, dedicated to providing high-quality medical services and advancing clinical research. Comprising a network of hospitals, primary care centers, and specialized facilities, the consortium aims to enhance patient care through innovative treatments and evidence-based practices. With a strong commitment to collaboration and excellence, Consorci Sanitari del Maresme actively sponsors clinical trials that contribute to medical knowledge and improve health outcomes for diverse populations. Their focus on research and development underscores their role as a key player in the healthcare landscape, fostering advancements in medical science and patient care.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Patients applied
Trial Officials
Jéssica Martínez Rodríguez
Principal Investigator
Consorci Sanitari del Maresme
Mateu Serra-Prat, PhD
Study Director
Consorci Sanitari del Maresme
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported