Cesarean Section
Conditions
Interventions
This is a randomized controlled clinical trial with placebo, with blind appraiser, with pre and post-application evaluations (immediately after the procedure and 30 minutes) of combined therapy in pos
Other
E02.565.280.945
E02.331
Sponsors
Universidade Federal Do Paraná
Maternidade Victor Ferreira do Amaral do Complexo do Hospital de Clínicas
Eligibility
Sex/Gender
Female
Age
15 Years to 45 Years
Inclusion criteria
Inclusion criteria: Women over 15 years of age;underwent cesarean during labor for at least 8 hours and a maximum of 24 hours after the procedure; post-cesarean pain
Exclusion criteria
Exclusion criteria: illiterate or non-oriented; presence of puerperal intercurrences such as: local bleeding requiring intervention, signs suggestive of infection, fever, anesthetic complications and breast intercurrences; diagnosis of epilepsy, demyelinating disease, spindle trauma, tumors, diabetes mellitus and hypertension; puerperal women who use pacemakers or implanted electronic devices; presence of local drainage system and; irritation or intolerance to the application of Combination Therapy (history of allergy or intolerance to the application of electrical current or therapeutic ultrasound)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The post-cesarean political situation during the immediate puerperium, controlled by the McGill questionnaire, from the observation of a variation of at least 5% in the pre and post-intervention measurements;A post-cesarean functional limitation during the immediate puerperium, selected by the Functional Capacity Check, based on the observation of a variation of at least 5% in the pre and post-intervention measurements | — |
Secondary
| Measure | Time frame |
|---|---|
| The painful condition during the immediate puerperium, verified by the McGill questionnaire, from the observation of a variation of at least 5% in the pre and post-intervention measurements in the period of 7 days;The functional limitation after cesarean section during the immediate puerperium, verified by the Functional Capacity Verification questionnaire, from the observation of a variation of at least 5% in the pre and post-intervention measurements in the period of 7 days | — |
Countries
Brazil
Contacts
Public ContactRaciele Guarda Korelo
Universidade Federal Do Paraná
Outcome results
None listed