Current partner codePEPTIDESDE
NCT05083910·Not applicable·INTERVENTIONAL

Randomization of Oxytocin, Oxytocin+Intrauterine Misoprostol and Carbetocin During C-section

Status

Completed

Phase

Not applicable

Enrollment

156

Locations

2

Results

Not posted

Publications

3

Study summary

What the protocol is testing.

Postpartum haemorrhage (PPH) remains an important cause of maternal morbidity and mortality and it accounts for approximately 25% of all deaths worldwide. Drugs such as oxytocin, carbetocin, misoprostol, prostaglandin F2a and methylergonovine have been tested for bleeding control during and after cesarean section. Oxytocin is the most widely used agent for the prevention of postpartum hemorrhage.The primary aim of this study is to reduce the mean blood loss during cesarean section.In this study, the investigators planned to compare peroperative and postoperative blood loss levels by giving oxytocin alone to the 1st group, oxytocin and intrauterine misoprostol to the 2nd group, and carbetocin to the 3rd group of patients who were randomly divided into 3 groups.In this study, we aimed to compare the efficacy of oxytocin, misoprostol and carbetocin in preventing uterine blood loss during cesarean section.

Full detailed description

Our prospective, randomized controlled study was conducted at the Department of Obstetrics and Gynecology of Bezmialem University Hospital between July and November 2021. The study protocol was approved by the Ethical Committee of the Medical Faculty of Bezmialem University. Written informed consent was obtained from all patients. We included a total of 156 women between 18 and 40 years of age who underwent a primary cesarean section or old 1 cesarean section under spinal anesthesia at term single pregnancy with an American Society of Anesthesiology physical status of I or II. This trial was designed and reported according to the Consolidated Standards of Reporting Trials (CONSORT) guidelines. The patients included in this study were randomly divided into three groups by random allocation using a computer-generated random number. Group I: Oxytocin(Synpitan forte®; Deva Pharma, Istanbul, Turkey) (n = 52 )( the oxytocin infusion consisting of 20 IU dissolved in 500 mL of normal 0.9 % sodium chloride solution and infused at a rate of 125 mL/h was administered immediately after clamping the umbilical cord). Group II: (n =52) oxytocin plus intrauterine misoprostol (Synpitan forte®; Deva Pharma, Istanbul, Turkey) (the oxytocin infusion was administered immediately after clamping the umbilical cord and misoprostol tablet (400 mg) was placed into uterine cavity at the fundus after delivery of the placenta and swabbing the cavity. Group III: (n =52) 100-mg carbetocin (Synpitan forte®; Deva Pharma, Istanbul, Turkey) was intravenously administered immediately after birth of the baby. All surgeries were performed by the same team of two surgeons.. The collected data were age, prepregnancy body mass index (BMI), gravida, parity, indication of cesarean section, gestational age at birth, Apgar scores at 1 and 5 min, birth weight, neonatal intensive care unit (NICU) admission, the preoperative hemoglobin and hematocrit concentrations, the change in the hemoglobin and hematocrit concentrations (difference between preoperative and postoperative levels), operating time, intraoperative blood loss. In this study, the investigators aimed to compare the efficacy of oxytocin, misoprostol and carbetocin in preventing uterine blood loss during cesarean section.

Interventions

Treatment arms and agents.

DRUG

I.V Oxytocin administration

Group I: Oxytocin( the oxytocin infusion consisting of 20 IU dissolved in 500 mL of normal 0.9 % sodium chloride solution and infused at a rate of 125 mL/h was administered immediately after clamping the umbilical cord). Group II:oxytocin plus intrauterine misoprostol (the oxytocin infusion was administered immediately after clamping the umbilical cord and misoprostol tablet (400 mg) was placed into uterine cavity at the fundus after delivery of the placenta and swabbing the cavity. Group III:100-mg carbetocin was intravenously administered immediately after birth of the baby.

Timeline

From registration to results.

  1. First posted

    Oct 19, 2021

  2. Study start

    Jul 1, 2021

  3. Primary completion

    Jan 22, 2022

  4. Study completion

    Jan 22, 2022

  5. Results posted

    Not reported

  6. Registry updated

    Jan 25, 2022

Outcomes

What the study measures.

Primary outcomes

Hemogram status

Time frame · Postoperative 8th hour

Postoperative hemogram status

Secondary outcomes

Blood Transfusion

Time frame · Postoperative 24th hour

Number of patients needing Blood Transfusion

Eligibility

Who can take part.

Minimum age
18 Years
Maximum age
40 Years
Sex
FEMALE
Healthy volunteers
Yes

Inclusion Criteria: * Single pregnancy greater than 37 weeks * Pregnant women between the ages of 18-40 Volunteer Exclusion Criteria: * Clinical diagnosis of Gestational diabetes * Clinical diagnosis of Gestational hypertension * Clinical diagnosis of preeclampsia * Clinical diagnosis of Placenta previa, * Clinical diagnosis of abruptio placenta * Conditions that cause excessive distention of the uterus (multiple pregnancies, severe polyhydramnios, fetal macrosomia, large fibroids displacing the cavity) Thrombophilia disorders, anticoagulation therapy History of major abdominal surgery

Study locations

2 registered sites.

Turkey (Türkiye). Showing up to 24 locations stored in the fast local snapshot.

Bezmialem Vakif University

Istanbul, Istanbulk, Turkey (Türkiye)

Bezmialem Vakif University

Istanbul, Turkey (Türkiye)

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Related PeptideStat pages

Put the record in context.

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