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Evaluation of the Benefits of Glucose Drinks During Childbirth (SOLISO)

C

Caen University Hospital

Status

Completed

Conditions

Childbirth

Treatments

Other: Glucose drink

Study type

Interventional

Funder types

Other

Identifiers

NCT01022697
2007-A00585-48

Details and patient eligibility

About

Fear of full stomach when emergency general anaesthesia is required is the origin of fastening when giving birth. This behaviour does not warranty perfect security for the general anaesthesia. In addition, well being for women and new born is affected. Giving birth is finally compared to a sportive competition with high-energy needs. As Intravenous energy intake is not regulated by physiologic digestion, it can induce metabolic disorders for the mother that can be amplified for the foetus.

Oral glucose drinks could offer some benefits:

  • gastric acidity would be decreased without significant increase in volumes.
  • energy intake would further more active and more efficiency labour
  • an increase in foetus well being

However, it has never been shown yet that such behaviour could offer those benefits. Also, it seems that there is not more vomiting, but most of the studies compared oral glucose intake to waterborne intake with the same volumes The expected efficacy is a reduction in labour duration and a reduction in percentage of extraction. Previous studies said that the lack of statistical power due to small number of subjects caused the absence of statistical significant relationship.

In addition, even though newborn have less acidosis, there is no clinical relationship proven.

The investigators propose a randomised multicentre study to assess efficacy of oral glucose drinks in comparison to traditional fastening when giving birth.

Main objective is to significantly reduce instrumental extraction rates. 5400 women will be included in the study in 2 years.

Enrollment

4,142 patients

Sex

Female

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Age >= 18 yrs
  • Entering for childbirth
  • Informed written consent

Exclusion criteria

  • more of 8 cm of dilatation
  • Caesarean section planned
  • natural delivery non-indicated
  • pre-partum hemostasis troubles
  • salicylic acid or anticoagulant treatment
  • pre-eclampsia or HELLP syndrome
  • diabetic neuropsy with troubles in gastric emptying
  • IMC > 40 at the end of pregnancy
  • understanding of the information
  • under guardianship

Trial design

4,142 participants in 2 patient groups

A
Active Comparator group
Description:
Glucose drink
Treatment:
Other: Glucose drink
B
No Intervention group
Description:
Fasting

Trial contacts and locations

9

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Data sourced from clinicaltrials.gov

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