Tranexamic Acid Infusion in Low Dose Versus in High Dose for Reducing Blood Loss in Radical Cystectomy Operations
Bleeding

About this trial
This is an interventional prevention trial for Bleeding
Eligibility Criteria
Inclusion Criteria:
- Age: 18 - 70 years old
- Gender: Males and females
- ASA grade I - II
- Patients undergoing radical cystectomy for bladder cancer regardless of tumor stage and histology.
- Patients who have undergone previous surgery, radiation, or chemotherapy may be included.
- All forms of urinary diversion are allowed
Exclusion Criteria:
- Patient refusal.
- Patient with allergy to tranexamic acid.
- Patients have thromboembolic disease (active or diagnosed within 1 year), such as deep vein thrombosis (DVT), pulmonary embolism (PE), cerebral thrombosis or MI.
- Pregnancy.
- Patients with hematuria.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Experimental
Active Comparator
Placebo Comparator
first group
second group
Third group
1st group (A) will include 30 patients: each one will receive 15mg/kg of I.V tranexemic acid as a bolus over 10 minutes (loading dose) then 10mg/kg/hour of I.V tranexemic acid as infusion all through the operation.
2nd group (B) will include 30 patients: : each one will receive 5mg/kg of I.V tranexemic acid as a bolus over 10 minutes (loading dose) then 1mg/kg/hour of I.V tranexemic acid as infusion all through the operation.
3rd group (C){controlled group} will include 30 patients: each one will receive saline (placebo) injection and infusion all through the operation.