Tranexamic acid for treatment of postpartum hemorrhage
Not Applicable
- Conditions
- terine atony.Other uterine inertia
- Registration Number
- IRCT2013052613473N1
- Lead Sponsor
- Qazvin University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 90
Inclusion Criteria
inclusion criteria:all women who were diagnosed as uterine atony by obstetrician following delivery;
exclusion criteria:history of any heart disease;liverdisease;kidney disease;history of any hematologic or Thrombophlebitis disease; Thromboembolism disease ;and all women who resieved general anesthesia during delivery.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The need for surgical intervention. Timepoint: Immediately after the intervention until discharge. Method of measurement: need to hypogastric Artery ligation, uterine artery ligation and hysterectomy based on Surgeon's visual judgment.;Bleeding volume after Atony. Timepoint: Immediatly after Atony. Method of measurement: Per cc and counts gazes and long gazes,and the volume of blood in suction.;Hemoglobin's changes. Timepoint: 6 and 24 hours after bleeding. Method of measurement: gr/dl with Spectrophotometer calibrated.;The need for blood products. Timepoint: After intervention until discharge. Method of measurement: based on unit and signs in surgen's examination or Hemoglobin less than 7.;Hospitalization. Timepoint: after delivery until discharge. Method of measurement: day.
- Secondary Outcome Measures
Name Time Method ousa/vomiting/thromoamboli. Timepoint: after delivery until release. Method of measurement: examination.