"Liposomal Encapsulated Vitamin C in Complex Regional Pain Syndrome"

Inclusion Criteria: * Female, Age \> 18 years * The woman of childbearing age - if applicable - must have a negative urine pregnancy test result and must agree to use adequate contraception (hormonal or barrier contraception method, or abstinence) during the study and one month later) * Consenting patient * Agrees to maintain the current level of physical activity throughout the study. * Agrees to avoid vitamins and supplements for 30 days before enrolment and during the study. * Avoid nutritious yeasts, whey protein, energy drinks, pomegranate, pomegranate juice, grapefruit, grapefruit juice and alcohol 7 days before enrolment and during the study * Willingness and ability to comply with scheduled visits, cellular phone calls, treatment plans, laboratory tests and completion of other study procedures specified in the protocol. Exclusion Criteria: * Pregnant, breastfeeding or considering pregnancy during the trial * Diabetic women * No renal lithiasis * No deficiency Glucose-6-phosphate dehydrogenase * Unstable medical conditions * Immunocompromised persons such as subjects who have undergone organ transplantation * Subjects who planned surgery during the clinical study * History of blood disorders / bleeding * Alcohol abuse (\> 2 standard alcoholic beverages per day) or drug addiction in the last 6 months * Participation in a clinical research trial within 30 days of randomization * Allergy or sensitivity to the product during the clinical study. * Persons who have a cognitive impairment and/or are unable to give an informed opinion. * Any other condition that, in the opinion of the physician, could affect the subject and lead to the successful completion of the study, action or pose a significant risk to the subject.