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Do Preoperative Carbohydrate Drinks Prevent Preoperative Catabolism in Mothers Undergoing Elective Caesarean Section? A Randomised Controlled Study

Not Applicable
Conditions
Caesarean Section
Starvation
Interventions
Dietary Supplement: Vitaflow Preload
Registration Number
NCT03220997
Lead Sponsor
NHS Greater Glasgow and Clyde
Brief Summary

The primary aim of this randomised control trial is to assess the impact of pre-operative carbohydrate loading on the incidence of urinary ketone bodies when compared to standard care in elective caesarean section. Half of the participants will receive pre-operative carbohydrates and the other half will receive standard care.

Detailed Description

Patients requiring general anaesthetic for surgical procedures are asked to stop eating and drinking for several hours before the procedure. This is due to concerns that such patients are at risk of lung damage caused by stomach contents entering their lungs while they are asleep (aspiration of gastric contents).

However, fasting patients for long periods of time can lower their ability to heal well and slow their recovery from surgery. Fasting increases anxiety levels and leads to poor patient satisfaction with the care received.

Recent studies have showed that allowing patients to drink clear, easily absorbed sugar rich liquids (carbohydrate drinks) until two hours prior to their anaesthetic does not expose them to extra risks while preventing the deleterious effects of starvation.

Carbohydrate drinks with a few other measures aimed at facilitating early recovery after surgeries are collectively termed Enhanced recovery after surgery (ERAS). The benefits and safety of enhanced recovery have been demonstrated in patients undergoing major bowel surgery and have been widely adopted. However, so far, no studies have been conducted to determine if these results apply to mothers undergoing planned caesarean sections. We hope to address this gap in the knowledge with our proposed study.

All mothers undergoing a planned caesarean section in the Princess Royal Maternity (PRM) will be invited to participate. Mothers will be divided into two groups. One group will receive standard care and the other group will receive a carbohydrate drink in addition to standard care. Information collected from the groups will be compared to evaluate the expected benefits and risks. The study will continue until the target sample size of 100 mothers in each of the two study groups is reached.

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
200
Inclusion Criteria
  • Mother scheduled for elective caesarean delivery at the Princess Royal Maternity Unit, Glasgow.
Exclusion Criteria
  • Patient refusal
  • Severe oesophageal reflux disease (persistent daytime and night-time reflux in association with documented structural damage i.e. Barrett's Oesophagus.)
  • Diabetes mellitus requiring treatment beyond dietary modulation
  • Unable to consent
  • Patients undergoing general anaesthetic should be excluded from the study.
  • Anticipated complex caesarean section patients.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
InterventionalVitaflow PreloadMothers will be given six sachets of carbohydrate powder to be mixed in water . Instructions will be given to have two sachets in 800ml water at 10pm the night before and one sachet in 400ml water at 6 am on the morning of surgery. The order of the list will be decided at 8.45am on the morning of surgery by the surgical team. Mothers scheduled to have surgery later than 11am will be given a further sachet at 9.30am. Mothers scheduled for surgery after 1pm will be given a sachet at 9am and 11am.
Primary Outcome Measures
NameTimeMethod
Incidence of urine ketone body levels at catheterisation prior to elective caesarean delivery.From insertion of urinary catheter until 5 minutes post urinary catherisation

After bladder catheterisation, urine will be tested for ketone bodies (Ketostix, Bayer)

Secondary Outcome Measures
NameTimeMethod
Preoperative thirstOn arrival to theatre - 5 minutes duration for questioning

Assessed via visual analogue scale

Preoperative hand grip strengthOn arrival to theatre and immediately prior to discharge from recovery room - 4 hour duration

Dominant hand grip strength measures with dynamometer

Length of hospital stayFrom admission to hospital until the date of discharge or date of death from any cause, whichever came first, assessed up to two weeks duration

Measured length of stay between hospital admission and discharge home

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