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 range18 Years
SexALL
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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)