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Preoperative Carbohydrate Drink Prior to Elective Caesarean Section

Preoperative Carbohydrate Drink Prior to Elective Caesarean Section: A Randomized Controlled Trial.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04159948
Enrollment
69
Registered
2019-11-12
Start date
2020-01-20
Completion date
2021-08-10
Last updated
2021-08-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fasting, Cesarean Delivery Affecting Fetus, Glucose, Low Blood

Keywords

Carbodydrate drink

Brief summary

Prior to caesarean section, patients should fast from solid food for 6 hours and from clear fluids for 2 hours. Carbohydrate drinks can also be consumed up to 2 hours before surgery. These drinks have been shown to improve patient well-being after surgery and may potentially improve the neonatal blood glucose level after delivery and reduce the risk of a low blood glucose level. This study aims to assess the influence of pre-operative carbohydrate drinks on blood glucose levels of the baby at delivery.

Detailed description

Patients recruited to the study will be randomised to one of 3 groups. Group 1 will receive standard care as per our current practice. This includes fasting from solids for 6 hours prior to surgery and clear fluids for up to 2 hours prior to surgery. Group 2 will receive a carbohydrate (CHO) drink preoperatively as well as adhering to standard care. Patients will be allowed to drink this CHO drink as required from admission to hospital on the morning of their surgery. They will also receive a further 400ml bolus at 2 hours prior to surgery. Group 3 will receive an apple juice drink preoperatively as well as adhering to standard care. Patients will be allowed to drink this apple juice drink as required from admission to hospital on the morning of their surgery. They will also receive a further 400ml bolus at 2 hours prior to surgery. Before the start of surgery, the patients non-dominant hand grip strength will be assessed using the dynamometer. Their subjective sense of thirst and hunger will be assessed. Their fasting times for food and fluids will be recorded. The patients' blood glucose will be measured from a blood sample as their intravenous cannula is inserted. The maternal urinary ketones will be measured from a urine sample upon insertion. The neonatal blood cord glucose will be measured from both an arterial and venous cord blood sample after delivery. This will be performed by the trained anaesthesia research fellow. Should hypoglycemia be identified, the hospital's neonatal hypoglycemia algorithm will be followed appropriately. The patients will be followed up at 24 hours by an outcome assessor blinded to the group allocation. Numerical rating scale (NRS) pain scores, postoperative nausea and vomiting and quality of recovery will be assessed at the patients beside. All neonates will be followed up to calculate admissions to neonatal unit and the number of glucose sachets required for hypoglycemia.

Interventions

DIETARY_SUPPLEMENTCarbohydrate drink

This is a commercially available pre-op carbohydrate drink used in enhanced recovery programmes.

Sponsors

Coombe Women and Infants University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Masking description

Patient will not be blinded to which arm they have been allocated to. Outcome assessors will be unaware of group allocation.

Intervention model description

3 arms with equal allocation.

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Elective caesarean section for singleton pregnancy under neuraxial anaesthesia. * Subjects able to give informed consent and willing to comply with the study protocol. * Subjects must be greater than 18 years old.

Exclusion criteria

* Diabetes Mellitus - including gestational diabetes. * Known foetal abnormality. * General anaesthesia. * Gestation \< 37 weeks. * Steroids received within 4 days of delivery. * Low birth weight 2.5 kg (IUGR) * BMI \> 40 kg/m2

Design outcomes

Primary

MeasureTime frameDescription
Neonatal cord blood glucose0 hoursA blood sample of the neonatal cord will be checked immediately after delivery.

Secondary

MeasureTime frameDescription
Number of neonatal rescue oral glucose sachets given.6 hoursContinuous - Number of neonatal rescue oral glucose sachets given.
Neonate requiring ICU admission and treatment for hypoglycemia6 hoursBinary - Neonate requiring ICU admission and treatment for hypoglycemia
Maternal blood glucose0 hoursMaternal blood glucose prior to the start of caesarean section.
Maternal urinary ketones0 hoursMaternal urinary ketones prior to the start of caesarean section.
Maternal subjective sense of thirst prior to the start of caesarean section.0 hoursScored on a scale 0-10
Maternal subjective sense of hunger prior to the start of caesarean section.0 hoursScored on a scale 0-10
Neonate tolerating 1st oral feeding.0-2 hoursBinary outcome - Neonate consuming adequate breast or bottle milk.
Resumption of oral diet post caesarean section.24 hoursTime until resumption of oral diet
Resumption of fluids post caesarean section.24 hoursTime until resumption of fluids
Post-operative nausea and vomiting (PONV)24 hoursThe self reported incidence of PONV
PONV requiring treatment24 hoursPONV requiring pharmacological treatment
Pain scores24 hoursPain scores at rest and movement on scale 0-10
Breastfeeding success24 hoursBinary - whether continuing attempted breast feeding at 24 hours
Maternal quality of recovery24 hoursMeasured using the ObsQoR-11 questionnaire

Countries

Ireland

Contacts

Primary ContactRuairi Irwin
r.irwin1987@gmail.com+353877497263

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026