Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03137810
Other study ID # Placental Cord Drainage versus
Secondary ID
Status Recruiting
Phase N/A
First received April 4, 2017
Last updated August 13, 2017
Start date January 1, 2017
Est. completion date November 30, 2017

Study information

Verified date August 2017
Source Ain Shams University
Contact Ahmed A ElShahawy, MD
Phone +2 01223266380
Email ahmedshafy@hotmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this work is to compare the effectiveness of placental cord drainage with no drainage in reducing the duration and blood loss in 3rd stage of labour.


Recruitment information / eligibility

Status Recruiting
Enrollment 180
Est. completion date November 30, 2017
Est. primary completion date November 1, 2017
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 38 Years
Eligibility Inclusion Criteria:

- Full term Uncomplicated singleton pregnancy Pregnancy with vertex presentation Patients expected to have spontaneous vaginal delivery

Exclusion Criteria:

- Over distended uterus(hydramnios.large fetus) Previous history of postpartum haemorrhage Known coagulation disorder Haemoglobin less than 8 g/dl Ante partum haemorrhage Multiple pregnancies Instrumental delivery

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
placental cord drainage
In the study group a of total number of 90 women placental end of the cut umbilical cord 1st will be clamped for few seconds and then unclamped and left open to drain blood in a vessel until flow stoped. This will prevent the drained blood from getting mixed with blood lost in the 3rd stage. Blood loss in the third stage will be measured using a Kelly's pad which will be used during delivery and the blood lost will be collected in a clean metal bowl which will be kept at the tail end of Kelley's pad.
non placemtal cord drainage
In 90 women after vaginal delivery of the baby placental end of the cut umbilical cord will be kept clamped.

Locations

Country Name City State
Egypt Ain shams university maternity hospital Cairo

Sponsors (1)

Lead Sponsor Collaborator
Ain Shams University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Duration of the third stage of labour within 15 min of delivery of baby
Secondary Amount of blood loss FIRST 24 HOURS
Secondary retained placenta 1ST HOUR OF DELIVERY
Secondary Manual removal of placenta 1HOUR OF DELIVERY
Secondary Changes in maternal haematocrit (Hct) after birth 1ST 24 HOURS
Secondary blood transfusion 1ST 24 HOURS
See also
  Status Clinical Trial Phase
Completed NCT00345254 - Severing Nuchal Cord at the Time of Delivery. Phase 1