The effect of using abdominal binder on clinical outcomes of cesarean sectio
- Conditions
- Cesarean.Delivery by elective caesarean section
- Registration Number
- IRCT2015042521917N2
- Lead Sponsor
- Vice chancellor for research, Tabriz University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 178
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.
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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 Outcome Measures
Name Time Method 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.