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

Primary Purpose

Myomectomy

Status
Completed
Phase
Phase 4
Locations
Egypt
Study Type
Interventional
Intervention
Tranexamic Acid
oxytocin
placebo
Sponsored by
Cairo University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Myomectomy

Eligibility Criteria

18 Years - 50 Years (Adult)FemaleDoes not accept healthy volunteers

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

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

tranexamic acid

oxytocin

placebo

Arm Description

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

Outcomes

Primary Outcome Measures

Intraoperative Blood loss
The total volume of intraoperative blood loss was estimated by measuring the amount of blood accumulated in the aspiration equipment and the amount of blood on the surgical gauze using an alkaline hematin technique

Secondary Outcome Measures

Operation time
Operation time from skin incision to skin closure in minutes.
Myomectomy time
Myomectomy time from first uterine incision to closure of last uterine incision in minutes

Full Information

First Posted
March 26, 2019
Last Updated
April 26, 2020
Sponsor
Cairo University
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1. Study Identification

Unique Protocol Identification Number
NCT03892668
Brief Title
Intravenous Oxytocin Versus Tranexamic Acid in Reducing Blood Loss During Abdominal Myomectomy.
Official Title
Safety and Efficacy of Intravenous Oxytocin Versus Tranexamic Acid in Reducing Blood Loss During Abdominal Myomectomy; A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
April 30, 2019 (Actual)
Primary Completion Date
February 1, 2020 (Actual)
Study Completion Date
March 15, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cairo University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Uterine leiomyomas (fibroids) are the most common benign tumors among women. Fibroids are found in approximately 20% of women over 35 years of age. In 20-50% of patients, fibroids may cause problems such as heavy menstrual bleeding, anemia, pelvic pain, pressure symptoms from extrinsic compression of the colorectal and urinary tract. Surgery is indicated for symptomatic uterine leiomyomas; hysterectomy for women who have completed childbearing (women > 40 years old), and myomectomy for women <40 years old who wish to preserve uterus and fertility.
Detailed Description
Interventions: Preoperative Full history, where demographic characteristics will be reported and examination to detect the size and mobility of uterus. Informed consent will be taken from patients. Trans-vaginal U/S to assess number, size, and types of myomas. Preoperative full labs (Hemoglobin, hematocrit, INR, liver enzymes and kidney functions) Intra Operative Preoperative antibiotics will be given before the beginning of the operation. The operations will be performed as standard through a midline or Pfannenstiel incision by the same consultant gynecologist to ensure consistency of study procedures. All patients will receive general anesthesia. After the skin incision, the subcutaneous fat and abdominal fascia will be opened crosswise, and the rectus muscle will be opened on the midline. The parietal peritoneum will be opened longitudinally to reach the pelvic cavity. Subsequently, a self-retaining retractor will be inserted, and intestine will be packed. The uterus will be inspected for the number, location, and shape of myomas. Other pelvic organs will be inspected for any associated pathology. When possible, uterine incisions will be performed on the anterior wall or fundus in order to reduce postoperative adhesions. The incision will be performed using monopolar diathermy. Intracapsular enucleation of myomas will be performed by gently dissecting between the myoma and the pseudo-capsule. The myoma will be gently enucleated out. Meticulous hemostasis will be secured by low-voltage coagulation of feeding vessels. Myoma bed will be closed by 1 or 2 layers of interrupted vicryl sutures (Vicryl 1-0 polyglactin 910; Egycryl, Taisier CO, Egypt). No mechanical tourniquet or local vasoocclusive drugs (e.g., vasopressin) will be used intraoperatively. The study will include patients scheduled for open abdominal myomectomy and will be divided into three equal groups. All the three groups will take a standard dose of 400 microgram of misoprostol rectally one hour before the operation. Postoperative Estimation of Hemoglobin 6 hrs postoperatively and next day morning. Monitor Vital Signs and need for blood transfusion. Send myomas for pathology.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Myomectomy

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
150 (Actual)

8. Arms, Groups, and Interventions

Arm Title
tranexamic acid
Arm Type
Experimental
Arm Description
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.
Arm Title
oxytocin
Arm Type
Active Comparator
Arm Description
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.
Arm Title
placebo
Arm Type
Placebo Comparator
Arm Description
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
Intervention Type
Drug
Intervention Name(s)
Tranexamic Acid
Intervention Description
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.
Intervention Type
Drug
Intervention Name(s)
oxytocin
Intervention Description
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.
Intervention Type
Drug
Intervention Name(s)
placebo
Intervention Description
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
Primary Outcome Measure Information:
Title
Intraoperative Blood loss
Description
The total volume of intraoperative blood loss was estimated by measuring the amount of blood accumulated in the aspiration equipment and the amount of blood on the surgical gauze using an alkaline hematin technique
Time Frame
during the operation
Secondary Outcome Measure Information:
Title
Operation time
Description
Operation time from skin incision to skin closure in minutes.
Time Frame
1 hour
Title
Myomectomy time
Description
Myomectomy time from first uterine incision to closure of last uterine incision in minutes
Time Frame
30 minutes

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
50 Years
Accepts Healthy Volunteers
No
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)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
AHMED SAMY, MD
Organizational Affiliation
Cairo University
Official's Role
Principal Investigator
Facility Information:
Facility Name
faculty of medicine Cairo university
City
Giza
ZIP/Postal Code
11231
Country
Egypt

12. IPD Sharing Statement

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

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