Cesarean. Delivery by elective caesarean section
Conditions
Interventions
Intervention 1: Intervention group:
After cesarean delivery, in addition to routine medical cares, the patient's abdomen will be fastened by Paksaman Abdominal Binder produced by Iran For intervention
Treatment - Other
Intervention group:
After cesarean delivery, in addition to routine medical cares, the patient's abdomen will be fastened by Paksaman Abdominal Binder produced by Iran For intervention group. For app
The control group will receive routine medical cares and medicine.
Sponsors
Vice chancellor for research, Tabriz University of Medical Sciences
Eligibility
Sex/Gender
Female
Age
18 Years to 35 Years
Inclusion criteria
Inclusion criteria: Inclusion Criteria: First or second parity; elective cesarean section; 18 to 35 years old; having literacy; term pregnancy, singleton and without complicated pregnancy; fannenstiel incision on the skin and Kerr Incision on the uterine; hemoglobin more than 11 g/dl during Pregnancy; no history of substance abuse and smoking; no presence of placenta previa or placenta accreta, Incerta, Percreta at ultrasound; no rupture of membrane more than 6 Hours; permission of gynecologist. Exclusion criteria: Intolerance of abdominal binder by participant; no tendency to continue the study; presence of essential disease based on mother`s report; increasing the duration of surgery more than one hour; simultaneous surgery such as hysterectomy, myomectomy and tubectomy; preeclampsia or eclampsia; presence of severe bleeding or bleeding leading to hysterectomy; presence of hemorrhagic disorders or use of anticoagulant drugs such as heparin or warfarin; tissues damage during cesarean delivery.
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Pain. Timepoint: Baseline, 6, 12, 18, 24, 48 hours and fifth day after intervention. Method of measurement: Visual Analogous Scale (VAS).;Distress. Timepoint: Baseline, 24 and 24 hours after intervention. Method of measurement: Symptom Distress Scale.;Hemoglobin and hematocrit levels. Timepoint: Baseline and 36 hours after intervention. Method of measurement: hemoglobin and hematocrit. | — |
Secondary
| Measure | Time frame |
|---|---|
| Healing of scar. Timepoint: Fifth day after cesarean section. Method of measurement: REEDA scale.;Consumed painkiller. Timepoint: 48 hours after cesarean section. Method of measurement: Calculation of number of consumed painkiller.;Satisfaction of participants. Timepoint: Fifth day after Cesarean. Method of measurement: Questionnaire. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactSevil Hakimi
Tabriz University of Medical Sciences
Outcome results
None listed