None listed
Conditions
Brief summary
This is a randomized, active-controlled, assessor- and statistician-blinded clinical study, with the purpose to assess the effectiveness and safety of oral administration of a mixture of diosmin, coumarin and arbutin (Linfadren®) in addition to conventional treatment, in the management of patients with post-trauma/surgery persistent hand edema. We hypothesize that managing patients with persistent hand edema following surgery/trauma is more effective by adding Linfadren supplementation to conventional treatment respect to conventional treatment alone
Interventions
Once eligible for the trial, participants will be recruited and randomised into one of the following 6-week interventions: 1) conventional rehabilitation treatment (control group) 2) conventional rehabilitation treatment plus Linfadren® (study group) a) conventional rehabilitation treatment consisting of elevation, cryotherapy, low-compression garments, retrograde massage, and gentle hand movement. These treatments were performed once a day for five days a week for six weeks, Patients will receive sessions with retrograde massage and gentle hand movement on a one-to-one basis with an experienced physiotherapist who also monitored the patients' adherence to the other treatments b) Linfadren® is a marketed supplement formulation which contains 200 mg of diosmin, 30.6 mg of coumarin, and 3.7 mg of arbutin. Coumarin (alpha-benzopyrones), stimulating macrophage activation and proteolysis, favors the reduction of excess stagnant proteins from tissues, with a decrease of edema and chronic inflammation. Diosmin (gamma-benzopyrones) is mainly a vascular-protecting agent, improving venous tone, protecting capillary bed microcirculation, reducing capillary permeability, but being potent inhibitors of inflammatory mediators as prostaglandin E2 (PGE2) and thromboxane A2 (TxA2), also exhibits anti-inflammatory properties. Arbutin is a natural product found in different plants including bearberry (Arctostaphylos uva-ursi) and has diuretic properties that help to reduce water tissue retention. Patients were instructed to consume Linfadren® on an empty stomach twice a day (6-hourly: 11a.m. and 5 p.m.) for two weeks, and once a day for four weeks. To improve adherence as far as medication assumption we asked patients to self-compile a daily diary.
Sponsors
Study design
Eligibility
Inclusion criteria
Inclusion criteria was: persistent hand edema with a difference of greater than or equal to 20mm between the affected hand and the unaffected hand in figure-of-eight measurement
Exclusion criteria
Exclusion criteria were: bilateral hand edema, pulmonary edema, congestive heart failure, coagulation defects, history of inflammatory, metabolic, or neuropathic arthropathies, treatment with anticoagulant drugs, any contraindications limiting clinical evaluation and therapy of the patient.