Comparative study between the effectiveness of Transcutaneous Electric Nerve Stimulation (TENS) and Low Power Laser devices in the scar incision in post-cesarean pai
Not Applicable
- Conditions
- Cesarean scarA10.165.450.300E04.520.252.500
- Registration Number
- RBR-3dv5t8
- Lead Sponsor
- Centro Universitário de Patos de Minas
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Female
- Target Recruitment
- Not specified
Inclusion Criteria
Postpartum women residing in Patos de Minas - MG, who are in the immediate puerperium (3 to 10 days postpartum), with pain at the incision site, with spinal anesthesia before the surgical procedure, absence of pathology will be included in the study genitourinary.
Exclusion Criteria
Patients with changes in sensitivity, demyelinating diseases, spinal cord trauma, hemorrhage, infection, fever, anesthetic complications, arterial hypertension will be excluded from the study.
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method