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OpenTrials
Completed

NCT Number: NCT03487341

Placental Cord Drainage After Vaginal Delivery

Placental Cord Drainage after Vaginal Delivery A randomized clinical trial

Completed

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Key information

Age range

18 year–40 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Ain Shams University Maternity Hospital

Cairo, Egypt

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Singleton pregnancy.
  • Pregnancy with vertex presentation.
  • Gestational age37 up to 42 weeks
  • Patient expected to have spontaneous vaginal delivery.
  • Maternal age 18 years old or more.

Exclusion criteria

  • Previous history of Postpartum hemorrhage.
  • Antepartum hemorrhage
  • Multiple pregnancies
  • Instrumental deliveries
  • Coagulation disorders
  • Over distended uterus (hydramnios, large fetus).
  • Patient with extensive extended vaginal or cervical tear.
  • Rupture uterus.
  • Secondary arrest of cervical dilatation.
  • Persistent occipito-posterior.
  • Deep transverse arrest of fetal head.

Treatment and study plan

Cord drainage

Other

Cord drainage

Cord clamping

Other

Cord clamping

Primary outcomes

  1. blood loss

    Time frame: 1 hour

Sponsors and collaborators

Lead sponsor

Ain Shams University

Other

Registry information

Official study title

Placental Cord Drainage After Vaginal Delivery: A Randomized Clinical Trial

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Apr 4, 2018
Registry last updated
Jan 29, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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