Delivery by elective cesarean section. Encounter for cesarean delivery without indication
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Spinal anesthesia Do not use anti-anxiety and hypnotic drugs and painkillers No underlying disease (neuromuscular disorders, hypertension, kidney disease, heart disease) BMI between 18/5 to 29/5 Term baby Uncomplicated pregnancy such as absence of eclampsia and preeclampsia Do not have any coagulation disorders or use anticoagulants Pfannenstiel incision on the skin and kerr incision on the uterus
Exclusion criteria
Exclusion criteria: Intolerance of the abdominal binder by the patient Reluctance to continue participating in the study Severe postoperative bleeding Damage to body tissues during cesarean section such as damage to the urinary tract and gastrointestinal tract
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: 6 hours after intervention, 12 hours after intervention, 18 hours after intervention and 24 hours after intervention. Method of measurement: Visual analog scale.;The amount of vaginal bleeding. Timepoint: Before intervention, 6 and 24 hours after intervention. Method of measurement: Measurement of hemoglobin and hematocrit using Complete Blood Count test.;Mobility. Timepoint: 12 and 24 hours after the intervention. Method of measurement: Six minute walk test. | — |
Secondary
| Measure | Time frame |
|---|---|
| Painkillers. Timepoint: 6, 12, 18 and 24 hours after the intervention. Method of measurement: Registration in the questionnaire based on patient records. | — |
Countries
Iran (Islamic Republic of)
Contacts
Esfahan University of Medical Sciences