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NCT Number: NCT02780245

Role of Tranexamic Acid Versus Uterine Cooling at Caesarean Section

This study aims to compare role of a prophylactic predefined intravenous Tranexamic Acid dose versus intraoperative Uterine Cooling in reducing blood loss and incidence of postpartum hemorrhage at secondary CS.

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Key information

About this study

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, as an antifibrinolytic agent. 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.

A recent study by Mitchell et al. concluded that Uterine cooling during cesarean delivery was efficient enough to decrease blood loss and the incidence of postpartum hemorrhage.

This study aims to compare role of a prophylactic predefined intravenous Tranexamic Acid dose versus intraoperative Uterine Cooling in reducing blood loss and incidence of postpartum hemorrhage at secondary CS.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Women who attended Talkha Central Hospital for planned or emergency secondary CS.
  • Singleton pregnancy at term with gestational age (G.A) between 38±5 and 40 weeks.

Exclusion criteria

  • Preoperative exclusion criteria were women who had any disorders of heart, liver, kidney, brain or blood, Abruptio placenta, placental abnormalities or accrete syndromes, Polyhydramnios, macrosomia, preeclampsia, allergy to TXA, history of thromboembolic disorders, or severe anemia.
  • Intraoperative exclusion criteria was inability to exteriorize the uterus during CS for group (Y).

Treatment and study plan

Tranexamic Acid

Drug

At 20 minutes preoperatively, TXA of 20 mg/kg was administered in Z Solution (500•0 ml normal saline containing a prophylactic antibiotic 1•0 g).

Other names: TXA

Intraoperative Uterine Cooling

Procedure

Intraoperatively immediately following delivery of the fetus the uterus was been externalized in the usual fashion, and the body of the uterus cephalad to the hysterotomy incision was been wrapped in sterile surgical towels saturated in sterile and iced normal saline. These towels came from a sterile cooling pot set to 30 degrees Fahrenheit. Iced saline-soaked towels was been kept in place for a minimum of 5 minutes and replaced at the discretion of the attending obstetrician until the hysterotomy is closed and the uterus is replaced into the patient's abdomen.

Primary outcomes

  1. Total blood loss volume

    Time frame: Up to 3 hours

    Estimation of Total Blood Loss Volume (ml) during CS and in the PACU.

Secondary outcomes

  1. Hematocrit value (Hct)

    Time frame: 6 hours postoperative period

    Estimating change in Pre- versus Post-operative hematocrit values (%) at 6 hours postoperatively.

  2. Overall blood loss volume greater than 1000 cc

    Time frame: Up to 9 hours

    Estimation of overall blood loss volume during CS and up to 6 hours postoperatively

  3. Need for Additional Ecbolics

    Time frame: Intraoperative

    Need for additional ecbolics to arrest and manage bleeding if there is a uterine atony

  4. Need for other surgical measures to stop bleeding

    Time frame: Intraoperative

    Need for other surgical measures to stop bleeding (B-lynch denoting uterine atony, uterine artery ligation, hysterectomy)

  5. Transfusion of Blood or Blood Products

    Time frame: Up to 3 hours

    Need for transfusion of blood or blood products during CS and in the PACU

Other outcomes

  1. Blood Pressure

    Time frame: Up to 3 hours

    Measuring maternal blood pressure (mmHg) immediately postoperative and after 3 hours postoperative.

  2. Maternal Side effects of intervention administered

    Time frame: Up to 9 hours

    Recording any Maternal side effects of interventions administered

  3. APGAR Scores

    Time frame: up to 2 hours

    Recording of APGAR Score (/10) for all neonates immediately after delivery

  4. Pulse Rate

    Time frame: Up to 3 hours

    Measuring maternal pulse rate (/minute) immediately postoperative and after 3 hours postoperative.

Sponsors and collaborators

Lead sponsor

Talkha Central Hospital

Other Gov

Registry information

Official study title

Tranexamic Acid Versus Novel Uterine Cooling Technique in Reducing Blood Loss and Incidence of Postpartum Hemorrhage at Caesarean Section

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
May 23, 2016
Registry last updated
Sep 5, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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