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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05080309
Other study ID # 21-0017
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date November 1, 2021
Est. completion date September 3, 2022

Study information

Verified date June 2021
Source University Hospital, Caen
Contact jean-luc hanouz
Phone 33 2 31 06 47 36
Email hanouz-jl@chu-caen.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Carbohydrate intake during physical exercise improves muscle performance and decreases fatigue. We hypothesized that carbohydrate intake during labor which is a period of significant physical activity can decrease the instrumental vaginal delivery rate. Following Siliso study we found a trend toward a decrease in instrumental vaginal delivery and the mount of carbohydrate intake durong labour. However due to some limitations no clear conclusion could be drawn. The present study is designed to examine the relationship between a high calory oral intake (>44 kCal/hour during labour) and the rate of instrumental delivery.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 600
Est. completion date September 3, 2022
Est. primary completion date September 1, 2022
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - nulliparous women - singleton pregnancy - social insurance - uncomplicated pregnancy - no contraindication to vaginal delivery Exclusion Criteria: - scheduled caesarean section - labor < 37 weeks of gestational age - cervical dilation > 8cm at inclusion - scheduled induced delivery - contraindication to pushing effort during labor and delivery - BMI > 40 kg/m2 - medical history of daibetes mellitus, hypertension, heart disease

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
carbohydrate oral intake
During labor the women will have free access to water and 20 ml commercial fruit juice bricks containing between 430 or 660 kcal/l. Every 2 hours the midwife or the nurse will measure the fruit juice oral intake volume and will advise women to drink the planned volume (1 brick/2hours)
Other:
free water only
Women will have free access to water only

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Caen

Outcome

Type Measure Description Time frame Safety issue
Primary instrumental vaginal delivery rate of instrumental vaginal delivery 2 days
Secondary oxytocin administration rate of oxytocin administration 2 days
Secondary caesarean section rate of caesarean section 2 days
Secondary nausea and vomiting rate of nausea and vomiting 2 days
Secondary thirst sensation on verbal rating scale self evaluation of thirst using a verbal rating scale from 0 (not thirst to 10 maximal thirst) 2 days
Secondary hunger sensation on verbal rating scale self evaluation of hunge rusing a verbal rating scale from 0 (no hunger to 10 maximal hunger) 2 days
Secondary fatigue self evaluation of fatigue using a verbal rating scale from 0 (0 no fatigue to 10 exhausted) 2 days
Secondary umbilical blood pH umbilical blood pH measured at child birth 1 min
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