DRUG
intravenous tranexamic acid
The tranexamic acid (TXA) group will receive a single bolus IV injection of 15 mg/kg of TXA 20 minutes before surgical incision
Status
Unknown
Phase
Phase 4
Enrollment
153
Locations
0
Results
Not posted
Publications
0
Study summary
the aim of the present study is to compare safety and efficacy of intravenous tranexamic acid versus IV carbetocin in reducing blood loss during abdominal myomectomy: a randomized controlled trial
Interventions
DRUG
The tranexamic acid (TXA) group will receive a single bolus IV injection of 15 mg/kg of TXA 20 minutes before surgical incision
DRUG
The carbetocin group will receive a single bolus IV injection of 100 mcg of carbetocin 20 minutes before surgical incision
DRUG
the placebo group will be given a normal saline IV bolus 20 minutes before surgical incision
Timeline
First posted
Apr 22, 2020
Study start
May 1, 2020
Primary completion
Oct 10, 2020
Study completion
Oct 20, 2020
Results posted
Not reported
Registry updated
Apr 22, 2020
Outcomes
intraoperative blood loss
Time frame · one hour
the intraoperative blood loss in ml will be estimated during the procedure
need for blood transfusion
Time frame · 24 hours
need for intraoperative or postoperative blood transfusion
Eligibility
Inclusion Criteria: * women with symptomatic fibroids candidate for abdominal myomectomy with staging of myoma from (3 to 6) according to FIGO staging Exclusion Criteria: * women with Myoma FIGO staging (1,2,7 and 8) candidate for laparoscopic or hysteroscopic myomectomy, women with allergy or contraindications to carbetocin or tranexamic acid
Study locations
No country data reported. Showing up to 24 locations stored in the fast local snapshot.
No study locations reported.
Publications
No PMID-linked publications were present in this registry snapshot.
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