Impact of Oral Carbohydrate Consumption Prior to Cesarean Section

Not Applicable

Completed

• Conditions: Dehydration
• Interventions: Dietary Supplement: Rehydration beverage; Dietary Supplement: Oral Carbohydrate Beverage

• Registration Number: NCT02684513
• Lead Sponsor: University of Florida

Brief Summary

For more than 15 years, traditional fasting regimens prior to scheduled surgeries have been called into question, yet prolonged preoperative fasting remains common practice. While prolonged fasting is aimed at reducing the risk of pulmonary aspiration, prolonged fasting is uncomfortable, has an inconsistent effect on gastric volumes and acidity and may lead to dehydration without a clear reduction in the incidence of aspiration. Fasting by itself decreases hepatic glycogen stores, induces a state of insulin resistance and impairs cardiovascular function. Yet, prolonged preoperative fasting remains common.

Preoperative oral carbohydrate (CHO) consumption improves insulin sensitivity and decreases the time to return of gut function without increasing gastric volumes or acidity compared to other clear liquids and fasting. Previous work has shown oral CHO consumption improves patient well-being to a greater degree than placebo drink (water or flavored water) and fasted controls. Oral CHO also outperforms a similar volume of intravenous glucose supplementation. These benefits have reduced hospital stays in a variety of surgical models by as much as 20%. Further, preoperative CHO supplementation improved postoperative patient hunger, thirst, anxiety, fatigue and nausea.

The purpose of this research study is to determine if drinking a high carbohydrate beverage before cesarean section surgery can improve patient well-being, compared to patients who drink a low carbohydrate beverage or fast before surgery.

Detailed Description

The study hopes to determine if either of two different oral beverages (a higher CHO concentration versus a lower CHO concentration) is superior to routine fasting in terms of preoperative well-being among patients presenting for scheduled cesarean section. Preoperative well-being will be determined by a composite of visual analog scale scores aimed at assessing hunger, thirst, anxiety, fatigue and nausea on the morning of surgery.

Women will be recruited from one of two outpatient obstetric clinics, University of Florida (UF) Health Women's Center - Medical Plaza or UF Health Women's Center. Women presenting for scheduled cesarean section will be provided with an opportunity to participate. Then the women will be randomized into one of three groups: oral carbohydrate beverage (group CHO), re-hydration beverage of an equal volume (group R) or fasted controls (group F). All subjects who consent to participation will have the following recorded: height, weight, age, indication for cesarean section, surgeon, and number of prior cesarean sections.

Study Timeline

• Study First Submitted: 2016-02-04
• Study First Submitted QC: 2016-02-12
• Study First Posted: 2016-02-18
• Study Start: 2016-06-14
• Primary Completion: 2018-06-12
• Study Completion: 2019-04-04
• Status Verified: 2019-07
• Last Update Submitted: 2019-07-30
• Last Update Posted: 2019-07-31

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 134

Inclusion Criteria

• Full-term (≥37 weeks gestation) with singleton gestation
• Proficient with English language
• Planning on undergoing scheduled cesarean delivery under neuraxial anesthesia

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Exclusion Criteria

• Women with pre-gestational or gestational diabetes mellitus or diabetes present prior to pregnancy
• Women who did not complete a gestational diabetes screening test
• Women who received steroids within the past 7 days prior to delivery
• Women who received magnesium sulfate in the setting of hypertensive disorders of pregnancy
• Women with a history of chronic opioid use
• Preterm pregnancies
• Fetuses with congenital abnormalities or growth restriction
• Multiple gestation
• Women who are American Society of Anesthesiology Class III or higher

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: FACTORIAL

Arm && Interventions

Group	Intervention	Description
Rehydration Beverage Group	Rehydration beverage	Subjects assigned to this group will receive 710 mL of re-hydration beverage the evening prior to surgery and 355 mL the morning of surgery.
Oral Carbohydrate Beverage Group	Oral Carbohydrate Beverage	Subjects assigned to this group will receive 710 mL of a preoperative beverage the evening prior to surgery and 355 mL the morning of surgery.

Primary Outcome Measures

Name	Time	Method
Change in preoperative well-being assessment from baseline to one hour using the 100 millimeter (mm) visual analogue scale.	Change from baseline to one hour	100 mm visual analogue scales for hunger, thirst, anxiety, fatigue and nausea administered on the morning of surgery prior to morning beverage consumption and 60 minutes after the beverage. All measurements will be assessed using the same scale starting at 0 to 100mm with 0 being the worst and 100 being the best and average being 85.

Secondary Outcome Measures

Name	Time	Method
Number of participants admitted to maternal intensive care unit between the groups	Up to 15 days	Number of ICU admissions during hospitalization between the groups
Number of days in the hospital for each participant between the groups	Up to 15 days	Number of days in the hospital for each participant between the groups. This will be measured by using the chi-square tests to assess the frequency of this outcome between the groups.
Number of neonates diagnosed with an infection between the groups.	Baseline	Number of neonates with an infection diagnosis. This will be measured by using the chi-square tests to assess the frequency of this outcome between the groups.
Changes between the maternal groups assessed by the mean arterial pressure (MAP) recordings in every 5 minute period	At time of surgery to the conclusion	Maternal cardiovascular function will be assessed by using the average of all the mean arterial pressure (MAP) recordings in every 5 minute period. This will be measured by using a student's t-test for significant differences between the groups.
Number of postoperative infections between the groups	Up to 15 days	Number of postoperative infections for each participant between the groups. This will be measured by using the chi-square tests to assess the frequency of this outcome between the groups.
Neonates with plasma glucose level of less than 45 mg/dL between the groups	Baseline	First umbilical cord blood sample will be taken for plasma glucose level of less than 45 mg/dL to note hypoglycemia between the groups.
Number of neonates on ventilation for 6 hours or greater between the groups	6 hours	Number of neonates on ventilation for 6 hours or greater will be recorded.
Number of neonates with a 5 minute Apgar score less than 7 between the groups	5 minutes	Record of the 5 minute apgar score \< 7. Apgar scores are as follows: between 7 and 10, means the neonate is in good shape, between 4 and 6 may need some help breathing, and 3 or less may need immediate lifesaving measures.
Number of neonates admitted to the intensive care unit (ICU) between the groups	Baseline	Number of neonates admitted to the ICU between the groups. This will be measured by using the chi-square tests to assess the frequency of this outcome between the groups.

Trial Locations

Locations (1)

UF Health; 🇺🇸 Gainesville, Florida, United States