Tranexamic Acid for Prevention of Hemorrhage in Cesarean Delivery (TXA)
Primary Purpose
Post Partum Hemorrhage, Fibrinolysis; Hemorrhage, Blood Loss
Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Tranexamic Acid
Placebo
Sponsored by
About this trial
This is an interventional prevention trial for Post Partum Hemorrhage focused on measuring Tranexamic acid, TXA, Anti-fibrinolytics, Postpartum hemorrhage, Obstetric hemorrhage, Fibrinolysis
Eligibility Criteria
Inclusion Criteria:
- Intrauterine pregnancy
- Age ≥ 18
- Gestation age ≥ 37 weeks 0 days
- Scheduled cesarean delivery
- Second or third cesarean delivery
- Singleton pregnancy
Exclusion Criteria:
- First cesarean delivery
- Four or more cesarean deliveries
- Intrauterine fetal death
- Fetal anomalies
- Documented coagulopathy (Elevated Prothrombin Time (PT), Elevated Partial Thromboplastin Time (PTT), Elevated International Normalized Ratio (INR))
- Thrombocytopenia (Platelet count < 100k)
- Internal bleeding, external bleeding, easy bruising
- History of thrombotic event
- Hypertension
- Diagnosis of renal insufficiency (Creatinine> 1 mg/dL)
- Insulin-treated diabetes
- Suspected morbidly adherent placenta
- Placenta previa
- Multiple Gestations
- BMI ≥ 50
- Hematocrit ≤ 25
- Blood transfusion within 24 hours prior to cesarean delivery
- History of abnormal bleeding or blood disorder
- Planned general anesthesia
Sites / Locations
- Parkland Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Tranexamic acid
Placebo
Arm Description
Tranexamic Acid for intravenous administration.
Normal saline for intravenous administration.
Outcomes
Primary Outcome Measures
Blood Volume Loss
Total blood volume loss will be calculated in milliliters.
Secondary Outcome Measures
D-Dimer (µg/mL)
Measured from blood sample collection.
Fibrinogen (mg/dL)
Measured from blood sample collection.
Tissue Plasminogen Activator Antigen (ng/mL)
Measured from blood sample collection.
Plasminogen Activator Inhibitor-Type-1 (Units/mL)
Measured from blood sample collection.
Rotational Thromboelastometry INTEM and EXTEM Clotting Time
Rotational thromboelastometry is a whole blood viscoelastic test that analyzes deficits in clotting factors, clot strength, and clot breakdown. EXTEM, INTEM, and FIBTEM tests measure the extrinsic pathway, intrinsic pathway, and fibrinogen levels, respectively. Compared to non-pregnant patients, FIBTEM/EXTEM/INTEM amplitudes and the FIBTEM maximum clot firmness are higher in pregnant women. The EXTEM and INTEM clotting time are shorter, indicating the relative hypercoagulability of pregnancy. Reference ranges for INTEM Clotting Time (100-240 seconds), INTEM Maximum Clot Firmness (50-72 millimeter), EXTEM Clotting Time (38-79 seconds), EXTEM Maximum Clot Firmness (50-72 millimeter), FIBTEM Maximum Clot Firmness (9-25 millimeter).
Rotational Thromboelastometry INTEM, EXTEM, FIBTEM Maximum Clot Firmness
Rotational thromboelastometry is a whole blood viscoelastic test that analyzes deficits in clotting factors, clot strength, and clot breakdown. EXTEM, INTEM, and FIBTEM tests measure the extrinsic pathway, intrinsic pathway, and fibrinogen levels, respectively. Compared to non-pregnant patients, FIBTEM/EXTEM/INTEM amplitudes and the FIBTEM maximum clot firmness are higher in pregnant women. The EXTEM and INTEM clotting time are shorter, indicating the relative hypercoagulability of pregnancy. Reference ranges for INTEM Clotting Time (100-240 seconds), INTEM Maximum Clot Firmness (50-72 millimeter), EXTEM Clotting Time (38-79 seconds), EXTEM Maximum Clot Firmness (50-72 millimeter), FIBTEM Maximum Clot Firmness (9-25 millimeter).
Full Information
NCT ID
NCT03856164
First Posted
February 21, 2019
Last Updated
January 12, 2021
Sponsor
University of Texas Southwestern Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT03856164
Brief Title
Tranexamic Acid for Prevention of Hemorrhage in Cesarean Delivery
Acronym
TXA
Official Title
Use of Tranexamic Acid for Prevention of Hemorrhage in Cesarean Delivery
Study Type
Interventional
2. Study Status
Record Verification Date
January 2021
Overall Recruitment Status
Completed
Study Start Date
June 17, 2019 (Actual)
Primary Completion Date
January 10, 2020 (Actual)
Study Completion Date
August 31, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Texas Southwestern Medical Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The investigators prepared a novel study of tranexamic acid (TXA) designed to estimate the quantity of blood loss in women undergoing elective repeat cesarean deliveries. This is the first trial to utilize a prophylactic dose of TXA prior to incision followed by a subsequent prophylactic dose at placental delivery in obstetric patients undergoing scheduled cesareans. The purpose of this study is to quantify blood loss during uncomplicated repeat cesarean deliveries with and without TXA. The central hypothesis is that TXA administration reduces blood loss and fibrinolysis in women undergoing repeat cesarean sections.
Detailed Description
Obstetric hemorrhage has been identified as a contributory cause for the United States' suboptimal and inequitable outcomes among pregnant women. As such, obstetric hemorrhage has become a formal focus point in a national agenda to improve maternal outcomes. Strategies to identify maternal hypovolemia and treating obstetric hemorrhage are undergoing organized scrutiny in many states including Texas. Tranexamic acid (TXA) treatment is receiving increased emphasis in obstetric care because TXA inhibits fibrinolysis. Increased clot stability offers the possibility of preventing blood loss (prophylaxis) as well as mitigating ongoing hemorrhage. TXA therapy has been principally studied in nonpregnant populations; results of studies in pregnant women have been lacking.
Tranexamic acid is an antifibrinolytic agent that acts as a competitive inhibitor at the lysine binding sites of plasminogen and inhibits the ability of protease plasmin to cleave the fibrin clot. In large randomized controlled trials, it has been reported to be effective in decreasing perioperative blood loss in a variety of circumstances primarily involving trauma patients. Shakur and co-authors in a trial of 20,000 non-pregnant trauma patients reported a significant reduction in all-cause mortality after TXA administration. In another large study (WOMAN Trial), 20,000 pregnant women with hemorrhage were randomized to TXA or placebo. TXA was associated with a significant decrease in death due to bleeding.
Tranexamic acid's role in treating hemorrhage have been widely studied in non-pregnant populations. Studies of TXA in obstetrics are limited. The American College of Obstetricians and Gynecologists believes the data is insufficient to recommend tranexamic acid for prophylaxis.
The investigators designed a randomized placebo-controlled trial comparing TXA dosing prior to incision for cesarean delivery with a repeat dose given at placental delivery. The purpose is to quantify blood loss during uncomplicated repeat cesarean deliveries with and without TXA. The investigators elected to study scheduled elective cesareans because such procedures are at low risk for profound hemorrhage. It is the intent to have a study cohort where the two treatment groups (TXA or placebo) are as comparable as possible, so the efficacy of TXA is not tested in women with highly variable volumes of obstetric hemorrhage.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Post Partum Hemorrhage, Fibrinolysis; Hemorrhage, Blood Loss
Keywords
Tranexamic acid, TXA, Anti-fibrinolytics, Postpartum hemorrhage, Obstetric hemorrhage, Fibrinolysis
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
110 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Tranexamic acid
Arm Type
Active Comparator
Arm Description
Tranexamic Acid for intravenous administration.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Normal saline for intravenous administration.
Intervention Type
Drug
Intervention Name(s)
Tranexamic Acid
Other Intervention Name(s)
Cyklokapron
Intervention Description
Two doses of Tranexamic Acid (1 gram), diluted in 100 cc of normal saline. Administered intravenously at least 10 minutes prior to skin incision and repeated immediately after placental delivery.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Normal Saline
Intervention Description
100 mL of normal saline. Administered intravenously at least 10 minutes prior to skin incision and repeated immediately after placental delivery.
Primary Outcome Measure Information:
Title
Blood Volume Loss
Description
Total blood volume loss will be calculated in milliliters.
Time Frame
24 hours postpartum.
Secondary Outcome Measure Information:
Title
D-Dimer (µg/mL)
Description
Measured from blood sample collection.
Time Frame
Collection prior to first drug infusion, immediately before second infusion and 24 hours postpartum.
Title
Fibrinogen (mg/dL)
Description
Measured from blood sample collection.
Time Frame
Collection prior to first drug infusion, immediately before second infusion and 24 hours postpartum.
Title
Tissue Plasminogen Activator Antigen (ng/mL)
Description
Measured from blood sample collection.
Time Frame
Collection prior to first drug infusion, immediately before second infusion and 24 hours postpartum.
Title
Plasminogen Activator Inhibitor-Type-1 (Units/mL)
Description
Measured from blood sample collection.
Time Frame
Collection prior to first drug infusion, immediately before second infusion and 24 hours postpartum.
Title
Rotational Thromboelastometry INTEM and EXTEM Clotting Time
Description
Rotational thromboelastometry is a whole blood viscoelastic test that analyzes deficits in clotting factors, clot strength, and clot breakdown. EXTEM, INTEM, and FIBTEM tests measure the extrinsic pathway, intrinsic pathway, and fibrinogen levels, respectively. Compared to non-pregnant patients, FIBTEM/EXTEM/INTEM amplitudes and the FIBTEM maximum clot firmness are higher in pregnant women. The EXTEM and INTEM clotting time are shorter, indicating the relative hypercoagulability of pregnancy. Reference ranges for INTEM Clotting Time (100-240 seconds), INTEM Maximum Clot Firmness (50-72 millimeter), EXTEM Clotting Time (38-79 seconds), EXTEM Maximum Clot Firmness (50-72 millimeter), FIBTEM Maximum Clot Firmness (9-25 millimeter).
Time Frame
Collection prior to first drug infusion, immediately before second infusion and 24 hours postpartum.
Title
Rotational Thromboelastometry INTEM, EXTEM, FIBTEM Maximum Clot Firmness
Description
Rotational thromboelastometry is a whole blood viscoelastic test that analyzes deficits in clotting factors, clot strength, and clot breakdown. EXTEM, INTEM, and FIBTEM tests measure the extrinsic pathway, intrinsic pathway, and fibrinogen levels, respectively. Compared to non-pregnant patients, FIBTEM/EXTEM/INTEM amplitudes and the FIBTEM maximum clot firmness are higher in pregnant women. The EXTEM and INTEM clotting time are shorter, indicating the relative hypercoagulability of pregnancy. Reference ranges for INTEM Clotting Time (100-240 seconds), INTEM Maximum Clot Firmness (50-72 millimeter), EXTEM Clotting Time (38-79 seconds), EXTEM Maximum Clot Firmness (50-72 millimeter), FIBTEM Maximum Clot Firmness (9-25 millimeter).
Time Frame
Collection prior to first drug infusion, immediately before second infusion and 24 hours postpartum.
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Intrauterine pregnancy
Age ≥ 18
Gestation age ≥ 37 weeks 0 days
Scheduled cesarean delivery
Second or third cesarean delivery
Singleton pregnancy
Exclusion Criteria:
First cesarean delivery
Four or more cesarean deliveries
Intrauterine fetal death
Fetal anomalies
Documented coagulopathy (Elevated Prothrombin Time (PT), Elevated Partial Thromboplastin Time (PTT), Elevated International Normalized Ratio (INR))
Thrombocytopenia (Platelet count < 100k)
Internal bleeding, external bleeding, easy bruising
History of thrombotic event
Hypertension
Diagnosis of renal insufficiency (Creatinine> 1 mg/dL)
Insulin-treated diabetes
Suspected morbidly adherent placenta
Placenta previa
Multiple Gestations
BMI ≥ 50
Hematocrit ≤ 25
Blood transfusion within 24 hours prior to cesarean delivery
History of abnormal bleeding or blood disorder
Planned general anesthesia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Olutoyosi Ogunkua, M.D.
Organizational Affiliation
UT Southwestern
Official's Role
Principal Investigator
Facility Information:
Facility Name
Parkland Hospital
City
Dallas
State/Province
Texas
ZIP/Postal Code
75235
Country
United States
12. IPD Sharing Statement
Plan to Share IPD
No
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Tranexamic Acid for Prevention of Hemorrhage in Cesarean Delivery
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