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Role Of Different Prophylactic Doses Of Intravenous Tranexamic Acid In Reducing Blood Loss At Caesarean Section

Primary Purpose

Hemorrhage of Cesarean Section and/or Perineal Wound, Postpartum Hemorrhage

Status
Completed
Phase
Phase 4
Locations
Egypt
Study Type
Interventional
Intervention
Normal Saline containing a prophylactic Antibiotic 1 g
Tranexamic Acid
Sponsored by
Talkha Central Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hemorrhage of Cesarean Section and/or Perineal Wound focused on measuring Caesarean Section, Tranexamic Acid, Postpartum Hemorrhage, Ecbolics

Eligibility Criteria

20 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Maternal average age of 20-40 years.
  • Singleton pregnancy at term between 38±5 days and 40 weeks.
  • Elective planned or emergency secondary lower segment caesarean sections (LSCS).

Exclusion Criteria:

  • Women with severe medical and surgical complications as any of the following will be excluded :

    • Heart, liver, kidney, or brain diseases, and blood disorders.
    • Abruptio placenta, and placental abnormalities or accrete syndromes.
    • Polyhydramnios, macrosomia, preeclampsia, or allergy to tranexamic acid.
    • History of thromboembolic disorders, or severe anemia.

Sites / Locations

  • Al-Azhar University, Faculty of Medicine for Boys ( Cairo ), Al-Hussein University Hospital

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Placebo Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

Placebo

T1

T2

T3

Arm Description

Will receive a placebo (10 ml of distilled water) in Z solution [500 ml of normal saline containing a prophylactic Antibiotic 1 g] (At 20 minutes preoperatively).

Will receive Tranexamic acid 15 mg/kg in Z solution [500 ml of normal saline containing a prophylactic Antibiotic 1 g] (At 20 minutes preoperatively).

Will receive Tranexamic acid 20 mg/kg in Z solution [500 ml of normal saline containing a prophylactic Antibiotic 1 g] (At 20 minutes preoperatively).

Will receive Tranexamic acid 25 mg/kg in Z solution [500 ml of normal saline containing a prophylactic Antibiotic 1 g] (At 20 minutes preoperatively).

Outcomes

Primary Outcome Measures

Total Blood Loss Volume
Estimating Total Blood Loss Volume (ml) during and after Caesarean Section, up to 6 hours post-operative.

Secondary Outcome Measures

Duration of surgery
Duration of Caesarean Section estimating (min)
Hemoglobin level (Hb)
6 hours post-operative hemoglobin level (mg/dL) estimating.
Maternal weight (W)
2 hours post-operative maternal weight (kg) estimating
Hematocrit value (Hct)
6 hours post-operative hematocrit value (%) estimating.
Need for blood or blood products transfusion
Need for other medical measures to arrest and manage bleeding (transfusion of blood or blood products)
Need for additional ecbolics
Need for other medical measures to arrest and manage bleeding if there is a uterine atony (more than five units of intravenous Syntocinon®)
Need for hysterectomy
Need for other surgical measures to arrest and manage bleeding (Hysterectomy)
Need for uterine artery ligation
Need for other surgical measures to arrest and manage bleeding (Uterine artery ligation)
Need for B-lynch
Need for other surgical measures to arrest and manage bleeding if there is a uterine atony (B-lynch)
APGAR Score
APGAR Score as index for any neonatal side effects of medications given
Any sign for developing a thromboembolic disorder (Maternal)
As index for any maternal side effects of medications given
Blood pressure
Measuring maternal blood pressure (mmHg) immediately postoperative and after 2 hours postoperative.
Pulse rate
Measuring maternal blood puse rate (/minute) immediately postoperative and after 2 hours postoperative.

Full Information

First Posted
April 4, 2016
Last Updated
June 14, 2016
Sponsor
Talkha Central Hospital
Collaborators
Al-Azhar University
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1. Study Identification

Unique Protocol Identification Number
NCT02739815
Brief Title
Role Of Different Prophylactic Doses Of Intravenous Tranexamic Acid In Reducing Blood Loss At Caesarean Section
Official Title
Comparative Study For Role Of Different Prophylactic Doses Of Intravenous Tranexamic Acid In Reducing Blood Loss At Caesarean Section: A Randomised Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
June 2016
Overall Recruitment Status
Completed
Study Start Date
April 2016 (undefined)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
June 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Talkha Central Hospital
Collaborators
Al-Azhar University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
This study aims to define a safe prophylactic intravenous TXA dose with an advantage over others in reducing total blood loss volume at secondary uncomplicated LSCS.
Detailed Description
Bleeding during vaginal or operative delivery is always of prime concern. Despite significant progress in obstetric care 125,000 women die from obstetric hemorrhage annually in the world. The incidence of CS is increasing, and the average blood loss during CS (1000 mL) is double the amount lost during vaginal delivery (500 mL). CS rate as high as 25-30% in many areas of the world. In Egypt the CS rate is 27.6 %, in United States of America, from 1970-2009 the CS rate rose from 4.5-32.9%, and declined to 32.8% of all deliveries at 2010. In spite of the various measures to prevent blood loss during and after CS, post-partum hemorrhage (PPH) continues to be the most common complication seen in almost 20% of the cases, and causes approximately 25% of maternal deaths worldwide, leading to increased maternal morbidity and mortality. Women who undergo a CS are much more likely to be delivered by a repeat operation in subsequent pregnancies. For women undergoing subsequent CS, the maternal risks are even greater like massive obstetric hemorrhage, hysterectomy, admission to an intensive care unit, or maternal death. Medications, such as oxytocin, misoprostol and prostaglandin F2α, have been used to control bleeding postoperatively. TXA is a synthetic analog of the amino acid lysine,10 as an antifibrinolytic agent it has roughly eight times the antifibrinolytic activity of an older analogue; ε-aminocaproic acid. It competitively inhibits the activation of plasminogen to plasmin, by binding to specific sites of both plasminogen and plasmin, a molecule responsible for the degradation of fibrin, a protein that forms the framework of blood clots. Its intravenous administration has been routinely used for many years to reduce or prevent excessive hemorrhage in various medical conditions or disorders (helping hemostasis), also during and after surgical procedures like benign hysterectomy, open heart surgeries, scoliosis surgery, oral surgery, liver surgeries, total hip or knee arthroplasty, and urology. It has been shown to be very useful and efficient in reducing blood loss and incidence of blood transfusion in these surgeries, and decreases the risk of death in bleeding trauma patients. It was also included in the World Health Organization (WHO) Model List of Essential Medicines. About its role in CS, some recent studies showed that TXA has advantage and useful effect safely in reducing blood loss and requirement of additional ecbolics. Its doses used intravenously to reduce blood loss at CS were a bolus of 1gm, 10 mg/kg, or 15 mg/kg which had an advantage over 10 mg/kg in anemic parturients. No defined safe prophylactic intravenous TXA dose being found in searching literature having an advantage over other doses in reducing total blood loss especially at secondary uncomplicated LSCS.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hemorrhage of Cesarean Section and/or Perineal Wound, Postpartum Hemorrhage
Keywords
Caesarean Section, Tranexamic Acid, Postpartum Hemorrhage, Ecbolics

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Will receive a placebo (10 ml of distilled water) in Z solution [500 ml of normal saline containing a prophylactic Antibiotic 1 g] (At 20 minutes preoperatively).
Arm Title
T1
Arm Type
Active Comparator
Arm Description
Will receive Tranexamic acid 15 mg/kg in Z solution [500 ml of normal saline containing a prophylactic Antibiotic 1 g] (At 20 minutes preoperatively).
Arm Title
T2
Arm Type
Active Comparator
Arm Description
Will receive Tranexamic acid 20 mg/kg in Z solution [500 ml of normal saline containing a prophylactic Antibiotic 1 g] (At 20 minutes preoperatively).
Arm Title
T3
Arm Type
Active Comparator
Arm Description
Will receive Tranexamic acid 25 mg/kg in Z solution [500 ml of normal saline containing a prophylactic Antibiotic 1 g] (At 20 minutes preoperatively).
Intervention Type
Drug
Intervention Name(s)
Normal Saline containing a prophylactic Antibiotic 1 g
Other Intervention Name(s)
Solution of Sodium Chloride 0.9 %
Intervention Description
500 ml of normal saline containing a prophylactic Antibiotic 1 g.
Intervention Type
Drug
Intervention Name(s)
Tranexamic Acid
Other Intervention Name(s)
TXA
Intervention Description
Tranexamic acid
Primary Outcome Measure Information:
Title
Total Blood Loss Volume
Description
Estimating Total Blood Loss Volume (ml) during and after Caesarean Section, up to 6 hours post-operative.
Time Frame
Up to 7 hours
Secondary Outcome Measure Information:
Title
Duration of surgery
Description
Duration of Caesarean Section estimating (min)
Time Frame
Up to One hour
Title
Hemoglobin level (Hb)
Description
6 hours post-operative hemoglobin level (mg/dL) estimating.
Time Frame
6 hours
Title
Maternal weight (W)
Description
2 hours post-operative maternal weight (kg) estimating
Time Frame
2 hours
Title
Hematocrit value (Hct)
Description
6 hours post-operative hematocrit value (%) estimating.
Time Frame
6 hours
Title
Need for blood or blood products transfusion
Description
Need for other medical measures to arrest and manage bleeding (transfusion of blood or blood products)
Time Frame
Up to 6 hours
Title
Need for additional ecbolics
Description
Need for other medical measures to arrest and manage bleeding if there is a uterine atony (more than five units of intravenous Syntocinon®)
Time Frame
Up to 6 hours
Title
Need for hysterectomy
Description
Need for other surgical measures to arrest and manage bleeding (Hysterectomy)
Time Frame
Up to 6 hours
Title
Need for uterine artery ligation
Description
Need for other surgical measures to arrest and manage bleeding (Uterine artery ligation)
Time Frame
Up to 6 hours
Title
Need for B-lynch
Description
Need for other surgical measures to arrest and manage bleeding if there is a uterine atony (B-lynch)
Time Frame
Up to 6 hours
Title
APGAR Score
Description
APGAR Score as index for any neonatal side effects of medications given
Time Frame
Up to 30 minutes
Title
Any sign for developing a thromboembolic disorder (Maternal)
Description
As index for any maternal side effects of medications given
Time Frame
One week
Title
Blood pressure
Description
Measuring maternal blood pressure (mmHg) immediately postoperative and after 2 hours postoperative.
Time Frame
Up to 2 hours
Title
Pulse rate
Description
Measuring maternal blood puse rate (/minute) immediately postoperative and after 2 hours postoperative.
Time Frame
Up to 2 hours

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Maternal average age of 20-40 years. Singleton pregnancy at term between 38±5 days and 40 weeks. Elective planned or emergency secondary lower segment caesarean sections (LSCS). Exclusion Criteria: Women with severe medical and surgical complications as any of the following will be excluded : Heart, liver, kidney, or brain diseases, and blood disorders. Abruptio placenta, and placental abnormalities or accrete syndromes. Polyhydramnios, macrosomia, preeclampsia, or allergy to tranexamic acid. History of thromboembolic disorders, or severe anemia.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Amro M. Hetta, MS Student
Organizational Affiliation
Al-Azhar University, Faculty of Medicine for boys (Cairo), Departments of OBS/GYN
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mahmoud E. Mohammed, Professor
Organizational Affiliation
Al-Azhar University, Faculty of Medicine for boys (Cairo), Departments of OBS/GYN
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Yehia A. Wafa, Chairman
Organizational Affiliation
Al-Azhar University, Faculty of Medicine for boys (Cairo), Departments of OBS/GYN
Official's Role
Study Chair
Facility Information:
Facility Name
Al-Azhar University, Faculty of Medicine for Boys ( Cairo ), Al-Hussein University Hospital
City
Cairo
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
Undecided
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Role Of Different Prophylactic Doses Of Intravenous Tranexamic Acid In Reducing Blood Loss At Caesarean Section

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