Comparison of short-term outcomes of two vertical incision in the abdomen and Millard in pregnant women with a previous two time cesarean surgery.
Phase 2
- Conditions
- Vertical incision and Millard in Pregnant women.
- Registration Number
- IRCT2012102211205N1
- Lead Sponsor
- Vice chancellor for research,Tabriz University of Medical Scienes
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 84
Inclusion Criteria
Term pregnancy;. history of cesarean section in term pregnancy for more than 2 times; not having an underlying disease such as diabetes or lupus;. not having severe preeclampsia;.no prolonged rupture of membranes (PROM)>= 12 hours, having no oprative bleeding;. Morbid obesity.
Exclusion craitria:Midwifery bleeding during surgery ;. including the atonic uterus and placenta acreta ;. placenta percreta ;. need to hysterectomy or ovariectomy ;. need for further explorationduring surgery an underlying disease leading tofutherbleeding ;. such as coagulative disease .Emergency case of midwifery.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Bleeding. Timepoint: At the end of the abdominal incision. Method of measurement: Using the site of action of counting gases.
- Secondary Outcome Measures
Name Time Method Time to move the patient lying down, sitting or walking. Timepoint: Every day until discharge. Method of measurement: Tolerable and intolerable pain and need medication and onset of breastfeeding to infants.;Pain scor. Timepoint: Every 4 hours after surgery until discharge. Method of measurement: Using visual analog scale.