Evaluation of the effect of using abdominal binder on the amount of vaginal bleeding, pain intensity and mobility after cesarean sectio

Not Applicable

Recruiting

Conditions: Delivery by elective cesarean section.
Encounter for cesarean delivery without indication

Registration Number: IRCT20211024052856N1

Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Recruiting

Sex: Female

Target Recruitment: 184

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

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

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
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 Outcome Measures

Name	Time	Method
Painkillers. Timepoint: 6, 12, 18 and 24 hours after the intervention. Method of measurement: Registration in the questionnaire based on patient records.