CClinicalTrials.gg
Status unknownNCT02319707Updated Sep 9, 2015

Management of the Third Stage of Labor

A Phase 3 interventional study of Oxytocin and Oxytocin in 100 ml NaCl 0.9% in Postpartum Hemorrhage, sponsored by Yariv yogev. Status unknown. Open to female participants aged 18 Years to 45 Years. Per ClinicalTrials.gov, last updated 2015-09-09.

Sponsored by Yariv yogev · Phase 3, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Sep 2015), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Phase 3
Study type
Interventional
Enrollment
500
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
Female
01

Study summary

To compare the efficacy of three different protocols of third stage management in preventing PPH.

Read the detailed description

The third stage of labor refers to the period following the completed delivery of the newborn until the completed delivery of the placenta. The length of the third stage and its complications are affected by the uterine contractility and the duration of placental separation. The normal duration of third stage in nulliparous as well as in multiparous women is less than 30 minutes. There is strong evidence supporting the routine administration of uterotonic agents for the prevention of post-partum hemorrhage (PPH), in order to enhance natural uterine contraction in the third stage of labor, thus reducing the occurrence of PPH by 40%.

There is a joint policy statement between the International Confederation of Midwives (ICM), the International Federation of Gynecology and Obstetrics (FIGO) and the World Health Organization (WHO), all of which recommend active management of the third stage of labor in order to prevent PPH. active management led to a reduction in PPH incidence, maternal Hemoglobin\<9g/dL and need for blood transfusion. (4-7).

Active management of the third stage of labor involves prophylactic uterotonic treatment, early cord clamping and controlled cord traction to deliver the placenta. (2) Oxytocin is the first agent of choice for PPH prophylaxis because of its high efficacy and a low incidence of associated side effects. (6-9). Cotter et al found that the use of Oxytocin for PPH prophylaxis in the third stage of labor decreased the rate of maternal blood loss greater than 500 ml by approximately 50%. (10).

Oxytocin route of administration is either intravenously (IV) or intramuscularly (IM), with no significant difference in PPH incidence (9). This is based on a pharmacokinetic research from 1972 which found no difference between the absorption rates in both routes of administration. Since then no further research targeting this question was preformed. (11-12). recent guidelines from WHO, FIGO and ICM all recommended the use of 10 IU Oxytocin IM. (4, 7,13).

Previous studies have investigated the effect of intra-umbilical vein Oxytocin injection in reducing blood loss during the third stage of labor. This route of administration directs treatment to the placental bed and uterine wall, resulting in earlier uterine contraction and placental separation. However, limited published literature is available evaluating the effect of umbilical vein oxytocin injection in routine practices for active management of the third stage of labor. A prospective, randomized controlled trial of 412 women found that intra-umbilical injection of oxytocin alongside active management of the third stage of labor significantly reduced postpartum blood loss and the duration of the third stage (14).

Other uterotonic agents including Syntometrine (IM), Ergometrine (IM or IV) and Misoprostol (IM), can be used in active management of the third stage of labor. However, high quality evidence regarding their efficacy compared to Oxytocin is scarce. (9-10)

02

Conditions studied

  • Postpartum Hemorrhage
03

In context

Postpartum Hemorrhage

446 studies on the registry are indexed under Postpartum Hemorrhage; 75 are open to participants now.

This study's planned enrollment of 500 is above the median of 146 across 341 interventional studies indexed under Postpartum Hemorrhage.

Browse Postpartum Hemorrhage studies →

Lead sponsor

Yariv yogev is the lead sponsor of 5 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Singleton pregnancy.
  • 34-41 weeks of gestation.
  • Maternal age between 18 and 45.

Exclusion criteria

Exclusion Criteria:

  • Women who enter delivery room during the active phase of labor (cervical dilatation greater than 5 cm)
  • Coagulation defects
  • VAS score>3 (pain score)
  • Women with early PPH
  • Suspected placental abruption
05

Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
500 participants (estimated)

Study arms

  • Experimental
    Intramuscular treatment:IV

    pregnant women, 34-41 weeks of gestation, which were treated with 10 IU of IM Oxytocin during the third stage of labor.

    Drug: Oxytocin

  • Experimental
    Combined treatment:IV+IM

    pregnant women, 34-41 weeks of gestation, which were treated with 10 IU of IM Oxytocin together with 10 IU of IV Oxytocin in 100 ml NaCl 0.9% during the third stage of labor.

    Drug: Oxytocin

  • Active comparator
    The control group

    pregnant women, 34-41 weeks of gestation, which were treated with 10 IU of IV Oxytocin in 100 ml NaCl 0.9% during the third stage of labor. (this is the routine practice in our department).

    Drug: Oxytocin in 100 ml NaCl 0.9%

Interventions

  • DrugOxytocin

    The study group: divided into two groups: • Intramuscular treatment: pregnant women, 34-41 weeks of gestation, which were treated with 10 IU of IM Oxytocin during the third stage of labor. • Combined treatment: pregnant women, 34-41 weeks of gestation, which were treated with 10 IU of IM Oxytocin together with 10 IU of IV Oxytocin in 100 ml NaCl 0.9% during the third stage of labor.

    Also known as: Pitocin

  • DrugOxytocin in 100 ml NaCl 0.9%

    The control group: pregnant women, 34-41 weeks of gestation, which were treated with 10 IU of IV Oxytocin in 100 ml NaCl 0.9% during the third stage of labor. (this is the routine practice in our department).

06

What researchers measure

Primary outcomes

  1. Change in Hemoglobin concentration during labor

    Time frame: first and second day after delivery

Secondary outcomes

  1. Blood count (CBC) on the first and second day after delivery

    Time frame: first and second day after delivery

07

Study locations

No study locations are listed for this record.

08

References and documents

Publications

  • Oladapo OT, Okusanya BO, Abalos E, Gallos ID, Papadopoulou A. Intravenous versus intramuscular prophylactic oxytocin for the third stage of labour. Cochrane Database Syst Rev. 2020 Nov 9;11(11):CD009332. doi: 10.1002/14651858.CD009332.pub4. PubMed 33169839 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 9, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02319707
Lead sponsor
Yariv yogev
Responsible party
Yariv yogev (Prof. Yariv Yogev Director, Division of obstetrics and delivery, Rabin Medical Center) — Sponsor-investigator
First posted
Dec 18, 2014
Start date
Sep 2015
Primary completion
Jan 2017 (estimated)
Completion
Jan 2017 (estimated)
Last update
Sep 9, 2015

Study contacts

Yariv Yogev, professor
Contact
yarivy@clalit.org.il
9723-9377490
Yariv Yogev, professor
principal investigator · Director, Division of obstetrics and delivery

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Sep 2015. You cannot join it, but the record below documents what was studied.

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