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Use of Tranexamic Acid After Vaginal Delivery with Episiotomy a RCT Placebo Control Trail

A

Assuta Ashdod Hospital

Status and phase

Completed
Phase 4

Conditions

Anemia
Episiotomy Wound
Hemoglobin
Early Postpartum Hemorrhage

Treatments

Drug: Tranexamic acid
Drug: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT05448456
0138-21-AA

Details and patient eligibility

About

The objective of this study is to assess the effect of TA treatment on decline in Hb levels following vaginal delivery with an episiotomy, compared to a control group not receiving TA.

Full description

Vaginal delivery is often characterized by excessive blood loss. Normal range of blood loss in uncomplicated vaginal delivery is up to 500 ml. Despite this, most women can adapt due to hemodynamic changes that occur during pregnancy Several factors during labor can promote major blood loss that may be defined as post-partum hemorrhage (PPH) Early PPH (E-PPH) is defined by the World Health Organization as "blood loss from the birth canal in excess of 500 ml during the first 24 hours after delivery E-PPH occurs in up to 6% of births and it is one of the main causes of maternal morbidity and mortality accounting for about 25% of maternal deaths worldwide Among morbidities, E-PPH can lead to post-partum anemia (PPA). PPA incidence is estimated between 50%-80% of women PPA is defined as level of hemoglobin (Hb) of 11 gr/dl one week after delivery Anemia is associated with fatigue, post-partum depression and is a significant health problem in women during the reproductive age .

One of the major causes of E-PPH is perineal trauma. Perineal trauma is present in up to 85% of births either due to an episiotomy or spontaneous tear or a combination of them both During the the second stage of labor, the midwife or the obstetrician may need to make a surgical incision (episiotomy) to increase the diameter of the vaginal outlet and facilitate the baby's birth This procedure is done with scissors or scalpel and requires repair by suturing (14). In the United States, episiotomy rate was 11.6% in 2012 In a study published by Alvarez et al in 2017, the average reduction in Hb was 1.46 ± 1.09 g/dl following vaginal delivery with a second degree tear but without an episiotomy and 2.07 ± 1.24 following vaginal delivery with an episiotomy and no perineal tear. The greatest reduction in Hb occurred among women with episiotomy and a third or fourth degree tear with a decrease of 3.1 ± 1.32 g/dl.

Different strategies have been described for preventing and treatment PPH, including active management of the third stage of labor, among them uterine massage and controlled cord traction in addition to oxytocin and the use of Tranexamic acid (TA) as PPH treatment Tranexamic acid (TA) is a lysine analog, which acts as an antifibrinolytic via competitive inhibition to the binding of plasmin and plasminogen to fibrin. TA reaches peak plasma concentration immediately after intravenous administration A meta-analysis evaluated the use of tranexamic acid after vaginal delivery for prevention of primary PPH. When used as prophylaxis within 10 min after vaginal delivery usually at the dose of 1 g IV, in addition to standard prophylaxis with oxytocin, tranexamic acid reduced the risk of primary PPH and the mean post-partum blood loss However there are no studies that evaluated the impact of TA on blood loss after vaginal deliveries with an episiotomy.

Enrollment

150 patients

Sex

Female

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. women aged 18-45
  2. 37-42 weeks gestation
  3. Singleton pregnancy
  4. Cephalic presentation

Exclusion criteria

  1. Any contra-indication for vaginal birth

  2. PPH risk factors

    1. Dysfunctional labor
    2. Over distended uterus (macrosomia ,Polyhydramnios,multiple gestation)
    3. Grand multiparity
    4. Chorioamnionitis
    5. Precipitous labor
    6. Operative delivery
    7. Prolonged second stage
  3. Previous pph

  4. Preeclampsia

  5. Placental abruption

  6. Previous cesarean delivery

  7. Thrombophilia or coagulopathy

  8. Allergy to TA

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

150 participants in 2 patient groups, including a placebo group

Hexakakapron group
Active Comparator group
Description:
women with an episiotomy after vaginal delivery
Treatment:
Drug: Tranexamic acid
control group
Placebo Comparator group
Description:
women with an episiotomy after vaginal delivery
Treatment:
Drug: Placebo

Trial contacts and locations

1

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Central trial contact

Atara De Porto Amrany, MD; Eran Barzilay, Md PhD

Data sourced from clinicaltrials.gov

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