Patients will be randomized into 2 groups: * Group 1:Patients undergoing PENS T6, who also received Probiotics, during 10 weeks. * Group 2: Patients undergoing PENS T6 during 10 weeks. They will not received Probiotics Weight loss after 10 weeks of treatmente will be assessed.
Patients will be randomized into 2 groups: * Group 1:Patients undergoing percutaneous electrical stimulation of dermatome T6 (PENS T6), who also received Probiotics (Adomelle 1 caps/12h), during 10 weeks. * Group 2: Patients undergoing PENS T6 during 10 weeks. They will not received Probiotics Weight loss after 10 weeks of treatmente will be assessed.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
20
The patients will receive Adomelle 1caps/12h during 10 weeks
The patients will undergo percutaneous electrical neurostimulation of dermatome T6 weekle, during 10 weeks
Weight loss
Weight loss after treatment will be assessed
Time frame: 10 weeks
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