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The investigators aim at comparing the efficacy of a 2 weeks supplementation by L-citrulline or beetroot juice to L-citrulline placebo or denitrated beetroot juice respectively on Raynaud's phenomenon severity. Raynaud's phenomenon severity will be assessed through the Raynaud Condition Score, daily frequency of attacks or cumulative attack duration (expressed as min) daily collected by patients in a diary. Each Volunteer will choose his own main outcome among these 3 criteria.
Full description
Raynaud's phenomenon (RP) is a clinical condition that follows an exaggerated vasoconstriction of extremities in response to a cold or emotional stress. Microvascular dysfunction and alteration of the endothelial NO-dependent vasodilatation pathway through NO synthases (NOS) represents one of the main mechanisms.
A pharmacological treatment in RP is proposed to patients when conservative measures are not efficient enough to control the symptoms: calcium channel blockers remains the first line, phosphodiesterase type 5 inhibitors as a second line treatment, while intravenous iloprost remains restricted to patients with digital ischaemia. Vasodilator therapies are commonly associated with side effects due to the non-specific systemic vasodilation that often result in permanent discontinuation. Many patients prefer complementary and alternative therapies, but none has proven its efficacy. Therefore, there is still room for improvement in the treatment of RP, and research is needed in this area.
Enrollment
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Inclusion criteria
BMI > 18
Active Raynaud's Phenomenon characterized by a clinical history of Raynaud's
Stable disease over the previous two months (i.e. recent diagnosis of SSc will be excluded)
Patients insured by a social security scheme or beneficiaries of such a scheme
Patients who have dated and signed the informed consent form
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
30 participants in 4 patient groups, including a placebo group
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Central trial contact
Adeline Paris; Charles Khouri
Data sourced from clinicaltrials.gov
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