Vitamin C with its antioxidant role has many indications. The objective of this study is to demonstrate that taking vitamin C as a preventive significantly reduces the occurrence of complex regional pain syndrome (CRPS) type 1 in the aftermath of a scheduled surgery of the upper limb.
The preventive role of vitamin C on the development of CRPS type 1 was already demonstrated in traumatology and foot surgery. The management of CRPS type 1 is long and expensive. A preventive care seems beneficial. Some studies already performed suggest a similar role in scheduled surgery of the upper limb, major provider of CRPS type 1.The aim of the study is to demonstrate a significant reduction of CRPS 1 when taking vitamin C during the perioperative period in upper limb surgery. It is a prospective, randomized, double-blind, with placebo use, in two parallel group, multicenter and national. Patients are followed by their surgeon, under the terms of monitoring their disease. Two visits are required: one at 6 months and at 12 months. The patients will be reviewed at least in the two consultations looking for CRPS type 1 according to the criteria of the International Association for the Study of Pain (IASP)
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
1,000
CHU Amiens
Amiens, France
RECRUITINGCHU Rouen
Rouen, France
NOT_YET_RECRUITINGCH Saint-Quentin
Saint-Quentin, France
NOT_YET_RECRUITINGAppearance of a complex regional pain syndrome (CRPS) 6 months after surgery
Comparison of the occurrence of participants with CRPS type 1, between the two arms
Time frame: 6 months after surgery
Appearance of a complex regional pain syndrome 12 months after surgery
Comparison of the occurrence of participants with CRPS type 1, between the two arms
Time frame: 12 months after surgery
Tolerance
Evaluation of tolerance of vitamin C in pre- and post-operative period by adverse events registration
Time frame: 6 months after surgery
Observance to treatment
The observance to the treatment is estimated based on an adherence form completed by the patient
Time frame: 6 months after surgery
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