L-Citrulline in Patients With Post-Polio Syndrome (NCT02801071) | Clinical Trial Compass
CompletedPhase 3
L-Citrulline in Patients With Post-Polio Syndrome
Switzerland30 participantsStarted 2016-06-14
Plain-language summary
The purpose of the study is to show that the intake of L-citrulline improves muscle function in patients with Post-Polio Syndrome (PPS).
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:
* Prior paralytic poliomyelitis with evidence of motor neuron loss
* A period of partial or complete functional recovery after acute paralytic Poliomyelitis
* Slowly progressive and persistent new muscle weakness or decreased endurance, with or without generalized fatigue, muscle atrophy, or muscle and joint pain. Symptoms that persist for at least a year
* Exclusion of other neuromuscular, medical and skeletal abnormalities as causes of symptoms
* Patients older than 18 years at time of Screening
* ambulant
* ability to walk 150m in the 6 min. Walking distance (6MWD)
* females of childbearing potential willing to use contraceptive during the study
Exclusion Criteria:
* Previous (3 months or less) or concomitant participation in any other therapeutic trial
* Use of L-citrulline or L-arginine within the last 3 months
* Known individual hypersensitivity to L-citrulline
* Known or suspected malignancy
* Other chronic disease or clinical relevant limitation of renal, liver, heart function according to discretion of investigator
* Pregnant or breast-feeding women
* Severe renal failure (calculated glomerular filtration rate (GFR) \< 30 ml/min)
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.