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Effect of early oral carbohydrate intake after elective caesarean delivery: a randomised controlled trial

Early maternal drinking after elective caesarean delivery: a randomised controlled trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031085
Enrollment
Unknown
Registered
2020-03-22
Start date
2020-07-21
Completion date
Unknown
Last updated
2022-08-30

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

Conditions

elective caesarean delivery

Interventions

Group CC:received 100 mL of oral functional beverage (ShuNeng) through a straw
Group C:ingested only 10 ml of mineral water through a straw

Sponsors

Department of Anesthesiology, Obstetrics and Gynecology Hospital affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: an age of 20–45 years, American Society of Anesthesiologists (ASA) physical status II, having followed the preoperative fasting guidelines (a minimum of 2 h for clear fluids, 6 h for a light meal, and 8 h for a meal that included fried or fatty food), normal body temperature before surgery, and ability to understand the rationale of the study.

Exclusion criteria

Exclusion criteria: 1. Maternal refusal; 2. Body mass index (BMI) > 35 kg/m2; 3. Mental or physical disability; 4. Pregnancy combined with significant medical illness (e.g., thyroid disease, hypertension, diabetes, neuromuscular disease, etc.) or ear diseases (e.g., otitis media, tympanic membrane perforation) affecting the measurement of core body temperature; 5. Pre-existing abnormal anatomy of the upper gastrointestinal tract (e.g., previous lower esophageal, gastric or upper abdominal surgery, hiatal hernia) or other known gastric emptying disorders; 6. Airway examination that revealed risk factors for difficult intubation (Mallampati class 3 or 4, interincisor distance 36.5 degree C immediately upon arrival at the postanesthesia care unit (PACU); gastric antral cross-sectional area (CSA) by ultrasound at baseline >10.3 cm2; 13. Intolerance to one of the study fluids. 14. Parturients who met the following conditions were also excluded from this study: postpartum hemorrhage requiring continuous special attention; perioperative infusion of magnesium sulfate; 15. Missing data for various reasons.

Design outcomes

Primary

MeasureTime frame
The tympanic membrane temperature;

Secondary

MeasureTime frame
The shivering degree;Thermal comfort scores;The self-reported scores for hunger;The self-reported scores for thirst;Maternal satisfaction;Gastric antral cross-sectional area (CSA) by ultrasound;Maternal blood glucose;

Countries

China

Contacts

Public ContactHuang Shaoqiang

Department of Anesthesiology, Obstetrics and Gynecology Hospital affiliated to Fudan University

timrobbins71@163.com+86 13918210787

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 10, 2026