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Postpartum Uterotonic Administration

The Effect of the Timing of Uterotonic Administration in the Third Stage of Labour on Postpartum Hemorrhage

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02495272
Enrollment
330
Registered
2015-07-13
Start date
2014-06-30
Completion date
2016-01-31
Last updated
2015-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Postpartum Bleeding

Keywords

Postpartum hemorrhage, Third stage of labour, Oxytocin, Uterotonics, Active management of third stage of labour

Brief summary

The investigators are planning to determine the effect of the timing of oxytocin administration on the amount of blood loss, necessity for additional medical or surgical interventions.

Detailed description

The investigators are studying the effects of the timing of intramuscular oxytocin administration in the third stage of labour. The investigators are measuring the postpartum blood loss: quantitatively in the postpartum 1st hour and indirectly by the decrease in the hemoglobin-haematocrit levels in the postpartum 24th hour. The investigators are monitoring the length of the third stage of labour, and the need for extra uterotonics and/or surgical interventions.

Interventions

DRUGOxytocin

Oxytocin 10IU Administered intramuscularly.

Sponsors

Kanuni Sultan Suleyman Training and Research Hospital
CollaboratorOTHER
Bagcilar Training and Research Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Cephalic presentation * Singleton pregnancy * Gestational age \>35 weeks, * In active labour. * Expected fetal birth weight 2500-4500 grams.

Exclusion criteria

* Acute Fetal Distress * Conversion to abdominal delivery * Persistent high blood pressure (\>140/90mmHg) * Placenta Previa * Ablatio placenta * Previous C-Section * Uterine scar * Postpartum hemorrhage in previous pregnancies. * Hydramnios * Maternal infection * Forceps/Vacuum Assisted deliveries * Abnormal placentation ( Placenta accreta, increta or percreta) * Coagulation Defects * Hemoglobin \< 8g/dl

Design outcomes

Primary

MeasureTime frameDescription
Postpartum blood loss >500ccParticipants will be followed for the duration of hospital stay, an expected average of 24 hourNumber of participants whose blood loss is higher than 500cc.
Postpartum blood lossParticipants will be followed for the duration of hospital stay, an expected average of 24 hourQuantitative collection of blood loss.

Secondary

MeasureTime frameDescription
Need for additional uterotonicsParticipants will be followed for the duration of hospital stay, an expected average of 24 hourAdditional uterotonics (Oxytocin 10IU; Cytotec tb Rectal and/or vaginal) were administered if postpartum blood loss \>500ml OR uterine atony was observed OR sudden excessive hemorrhage was encountered.
Duration of the third stage of labour.Participants will be followed for the duration of labor unit stay, an expected average of one hour
Manual removal of the placenta.At first hour after delivery of the fetus
Postpartum transfusionParticipants will be followed for the duration of hospital stay, an expected average of 24 hour.
Drop in the hemoglobin and hematocrit levelsAt the 24th hour,postpartum

Countries

Turkey (Türkiye)

Contacts

Primary ContactDogukan Yildirim, MD
dogukanyildirim@yahoo.com+905063284383
Backup ContactEser S Ozyurek, MD
eozyurek@yahoo.com+905309322345

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026