Skip to content

Safety Assessment and Optimization of Fasting Before Procedural Sedation in Children Using Gastric Ultrasound

Safety Assessment and Optimization of Fasting Before Procedural Sedation in Children Using Gastric Ultrasound

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101361
Enrollment
Unknown
Registered
2025-04-24
Start date
2025-05-01
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Fasting Strategies for Pediatric Procedural Sedation

Interventions

Regular fasting group:Fasting strategy before sedation: Clear liquids for at least 2 hours, breast milk for at least 4 hours, formula milk, cow's milk, and easily digestible light meals for at least 6
Shorten the fasting group:Fasting strategy before sedation: Clear liquids for at least 1 hour, breast milk for at least 2 hours, formula milk, cow's milk and easily digestible light meals for at least

Sponsors

Gansu Provincial Maternity and Child-care Hospital (Gansu Provincial Central Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0.5 Years to 12 Years

Inclusion criteria

Inclusion criteria: (1) Children aged from 6 months to 12 years old; (2) American Society of Anesthesiologists Physical Status (ASA-PS) class 1-2; (3) Children who are scheduled to undergo an MRI examination and need to receive procedural sedation due to clinical requirements.

Exclusion criteria

Exclusion criteria: (1) Patients with abnormal gastrointestinal functions or related diseases (such as nausea and vomiting, gastroesophageal reflux, intestinal obstruction, etc.); (2) Patients with acute or chronic diseases that may affect gastric emptying (such as diabetes mellitus, severe obesity, neurological diseases, etc.); (3) Patients with airway abnormalities or diseases leading to ventilation difficulties (such as micrognathia, laryngomalacia of the airway, sleep apnea syndrome, etc.); (4) Patients who have used medications that may affect gastrointestinal motility prior to sedation; (5) Patients who refuse to cooperate with the ultrasound examination or are unable to complete the study due to other reasons.

Design outcomes

Primary

MeasureTime frame
The cross-sectional area of the antrum;The gastric volume;Perlas' grading;

Secondary

MeasureTime frame
Depth of sedation;Comfort score;Parents' satisfaction degree;Blood glucose;

Countries

China

Contacts

Public ContactQuanlong Fan

Gansu Provincial Maternity and Child-care Hospital (Gansu Provincial Central Hospital)

fan_insomnia@qq.com+86 139 1915 8479

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026