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Comparison of Effects of Sublingual Misoprostol and Infusion Oxytocin in Reduction of Bleeding at Cesarea

Phase 2
Conditions
Child birth and priperium.
O60-O75
O00-O99
Registration Number
IRCT201109104025N4
Lead Sponsor
Vice chancellor for research of Kermanshah University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
180
Inclusion Criteria

Inclusion criteria:Elective or Emergency Cesarean Deliveries with Incision in Lower Segment of uterus, Gestational Age more than 37 Weeks
Exclusion criteria:Anemia;Multiple pregnancy;Polyhydraminus;Prolonged labor;Premature rupture of membrane, History of diabetes mellitus,Hypertension,Cardiovascular disease,coagulopathy disorders, Placenta Previa & Placenta Abruption, Vaginal Bleeding.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Intraoperative bleeding. Timepoint: At the time of surgery. Method of measurement: Measured with the blood suctioned in cc by the graded container.
Secondary Outcome Measures
NameTimeMethod
Fever. Timepoint: During 48 hrs after surgery, measured every 3 hours. Method of measurement: Persist fever more than 38 ° c, with thermometer.;Change in basal pulse rate. Timepoint: Before surgery & intraoperative & 6 hrs after surgery. Method of measurement: Pulse rate in one minute.;Changing of blood pressure. Timepoint: Before surgery & intraoperative & 6 hrs after surgery. Method of measurement: Measuring with Sphygmomanometer.;Diarrhea. Timepoint: Before & 6 hrs after surgery. Method of measurement: question about change in frequency of defecation or its consistency (watery stool).;Vomiting. Timepoint: Before & 6 hrs after surgery. Method of measurement: Question about forceful expulsion of stomach contents.
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