Intradialytic Exercise Combined With Creatine Monohydrate in Patients With Chronic Kidney Disease… (NCT07666815) | Clinical Trial Compass
RecruitingPhase 1/2
Intradialytic Exercise Combined With Creatine Monohydrate in Patients With Chronic Kidney Disease Undergoing Hemodialysis.
Mexico48 participantsStarted 2026-03-02
Plain-language summary
This study aims to evaluate the effects of creatine monohydrate supplementation and an intradialytic exercise program on body composition, biochemical parameters, and functional capacity in patients with chronic kidney disease (CKD) undergoing maintenance hemodialysis. The study will compare the independent and combined effects of these interventions over an 8-week period to determine their potential benefits in this patient population.
Who can participate
Age range
18 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* atients who are treated at the State Haemodialysis Centre.
* Patients who receive haemodialysis three times a week.
* Signature of informed consent.
* Patients over 18 years of age, both men and women.
* Patients who have been on haemodialysis for no more than two years.
Exclusion Criteria:
Patients who have had a limb amputated.
* Patients who are in a state of anuria.
* Inability to perform muscular resistance or aerobic resistance exercises.
* Patients unable to perform physical exercise.
* HIV-positive patients. Elimination.
* Patients who voluntarily withdraw from the project.
* Inability to perform physical exercise.
* Death.
* Adverse events related to creatine consumption.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
What they're measuring
1
Grasping muscle strength
Timeframe: From baseline assessments through the end of the 8-week intervention
Trial details
NCT IDNCT07666815
SponsorPedro Julian Flores Moreno
Sponsor typeOTHER
Study typeINTERVENTIONAL
Primary completion2026-07-22
Contact for this trial
Israel Pérez Palafox PALAFOX Master of Medical Sciences