Actively Recruiting
Preoperative Carbohydrate Drink in Adolescent Idiopathic Scoliosis Surgery: the Impact on Safety and Enhanced Recovery
Led by University of Malaya · Updated on 2025-05-11
60
Participants Needed
2
Research Sites
59 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of this interventional study is to learn if carbohydrates loading improves overall outcome in adolescent patient undergoing scoliosis curgery The main questions of the study are as follows: 1. Does carbohydrates loading improves gastrointestinal related problems such as improvement in return of bowel function measured by first passage of flatus, reduce constipation by patient's time to first bowel opening and reduce incidence of post post operative nausea and vommiting 2. Does carbohydrates loading reduces length of hospital stay and patient's overall condition in term of anxiety, thirst and hunger 3. Does carbohydrates loading affects gastric residual volume by measuring residual gastric volume with ultrasound
CONDITIONS
Official Title
Preoperative Carbohydrate Drink in Adolescent Idiopathic Scoliosis Surgery: the Impact on Safety and Enhanced Recovery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient diagnosed with idiopathic scoliosis undergoing single-staged posterior spinal fusion
- Age between 10 to 19 years old
- ASA (American Society of Anesthesiologists) physical status class 1 or 2
You will not qualify if you...
- Diagnosis of diabetes mellitus (type I or type II)
- Intellectual disability
- ASA physical status class 3 or higher
- Significant risk of aspiration including hiatal hernia, GERD, BMI greater than 35 kg/m2, poor Glasgow Coma Scale, swallowing abnormalities, or gastrointestinal abnormalities
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 2 locations
1
University Malaya Medical Centre
Kuala Lumpur, Kuala Lumpur, Malaysia, 50603
Actively Recruiting
2
University Malaya
Pantai Valley, Kuala Lumpur, Malaysia, 59100
Actively Recruiting
Research Team
S
Siti Nadzrah B Yunus, MBBS
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
PREVENTION
Number of Arms
2
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