Status:

COMPLETED

Does Warming Mothers During Cesarean Delivery Help Keep Babies Warm When Delivered?

Lead Sponsor:

University of British Columbia

Conditions:

Cesarean Delivery

Eligibility:

FEMALE

19+ years

Phase:

NA

Brief Summary

The purpose of this study to investigate whether using a special warming blanket during Cesarean delivery helps maintain a normal body temperature in the baby when compared to mothers that are not war...

Detailed Description

Maternal hypothermia during Cesarean delivery is predominately caused by a combination of neuraxial anesthesia and exposure of abdominal contents and skin to the low temperatures of the operating room...

Eligibility Criteria

Inclusion

  • All women undergoing elective cesarean delivery under spinal anesthesia or combined spinal epidural anesthesia
  • Greater than 28 weeks gestation
  • ASA 1 \& 2 classification of health
  • Mothers presenting to the assessment or labour and delivery unit with ruptured membranes or early signs of labour, but not in active labour, who are not planned for a vaginal birth and who need an urgent cesarean delivery
  • Potential subjects need to be able to read and understand English unless independent (non-partner) translator available

Exclusion

  • Mothers in active labour - 3cm or more dilated with regular coordinated contractions
  • ASA 3 or above
  • Emergency cesarean delivery for fetal heart rate abnormalities
  • Cesarean delivery under general anesthesia
  • Maternal age \<19 years
  • Maternal infection
  • Mothers with a CSE where \> 5ml of epidural local anesthetic is given prior to the delivery of the fetus
  • Mothers with vascular disease - with the exception of hypertension/pre-eclampsia
  • Mothers with Type I Diabetes Mellitus
  • Untreated hypothyroidism or hyperthyroidism
  • Mothers with a history or family history of malignant hyperthermia
  • Those who cannot understand English, and lack of consent

Key Trial Info

Start Date :

February 1 2008

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

July 1 2008

Estimated Enrollment :

70 Patients enrolled

Trial Details

Trial ID

NCT00616174

Start Date

February 1 2008

End Date

July 1 2008

Last Update

March 17 2014

Active Locations (1)

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Page 1 of 1 (1 locations)

1

BC Women's Hospital

Vancouver, British Columbia, Canada