Actively Recruiting

Phase Not Applicable
Age: 18Years - 35Years
FEMALE
Healthy Volunteers
NCT07279545

The Effect of Placental Cord Drainage on the Third Stage of Labor and the Amount of Postpartum Bleeding

Led by Saglik Bilimleri Universitesi Gulhane Tip Fakultesi · Updated on 2025-12-12

80

Participants Needed

1

Research Sites

32 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of the study was to evaluate the effect of controlled placental cord drainage by opening the clamp at the maternal end after the umbilical cord is cut during birth on the duration of the third stage of labor (departure of the placenta), the amount of blood loss in the third stage, the amount of bleeding in the 2nd hour postpartum, and the development of postpartum complications.

CONDITIONS

Official Title

The Effect of Placental Cord Drainage on the Third Stage of Labor and the Amount of Postpartum Bleeding

Who Can Participate

Age: 18Years - 35Years
FEMALE
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • No problem speaking and understanding Turkish
  • Low-risk pregnant women
  • Vertex presentation
  • 37-41st weeks of gestation
  • No complications in mother or baby that prevent normal birth
  • Pain score less than 3 at study admission indicating low pain and good decision-making ability
Not Eligible

You will not qualify if you...

  • History of postpartum hemorrhage in participant or her mother or sister
  • Birth interval less than 2 years
  • Use of anticoagulants during pregnancy
  • Smoking during pregnancy
  • Low hemoglobin values (Hb < 11 g/dL)
  • Hematocrit less than 30

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Zonguldak Maternity and Child Diseases Hospital

Zonguldak, Zonguldak/Centre, Turkey (Türkiye), 67030

Actively Recruiting

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Research Team

S

Sinem GÜLTEKİN, Phd

CONTACT

N

Nazan KARAHAN, Prof. Dr.

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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