Intravenous Oxytocin Versus Tranexamic Acid in Reducing Blood Loss During Abdominal Myomectomy.
Myomectomy

About this trial
This is an interventional prevention trial for Myomectomy
Eligibility Criteria
Inclusion Criteria:
• Age group (18-50) years old
- Intramural or interstitial myomas (more than 5 cm)
- Symptomatic myomas (heavy menstrual bleeding or pain during menstruation)
- Abdominal myomectomy
- No medical disorders
- No coagulation disorders
Exclusion Criteria:
• Age group (less than 18 yrs old)
- Age group (more than 50 yrs old)
- Subserous or submucous myomas
- Laparoscopic or hysteroscopic myomectomy
- Medical disorders (for example uncontrolled hypertension, diabetes mellitus, renal or hepatic disorders)
- Coagulation disorders
- Previous use of anticoagulant drugs
- Previous myomectomy
- Allergy to Tranexamic acid or oxytocin
- Malignant features by U/S or examination
- Pregnancy
- Previous hormonal therapy (GnRH analogues)
Sites / Locations
- faculty of medicine Cairo university
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
Placebo Comparator
tranexamic acid
oxytocin
placebo
Patients in the TXA group will be given 15 mg/kg of tranexamic acid (Cyklokapron@; Amoun Pharmaceutical Co., SAE) slowly intravenously 30 min before surgery followed by 10 mg/ kg/h infusion in 500 ml Ringer's by infusion pump till the end of the procedure.
An equal volume of normal saline syringe in a double blinded manner will be intravenously administered to the OXYtocin group 30 min before surgery and will be followed by one ampoule of oxytocin (10 U/mL/amp) (Syntocinon; Aventis Pharmaceutical Co.) will be added to 500 mL Ringer's solution running at a rate of 400 mU/min by infusion pump till the end of the procedure.
An equal volume of normal saline syringe in a double blinded manner will be intravenously administered to the oxytocin group 30 min before surgery and will be followed by 500 ml saline infusion during the operation