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Bedside ultrasound assessment of gastric content and volume in full-term pregnant women with different fasting and water-deprivation durations: a prospective cohort study

Bedside ultrasound assessment of gastric content and volume in full-term pregnant women with different fasting and water-deprivation durations: a prospective cohort study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800018181
Enrollment
Unknown
Registered
2018-09-04
Start date
2018-09-30
Completion date
Unknown
Last updated
2018-09-10

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

Conditions

pregnant

Interventions

no-eating group (group N):duration of fasting and water-deprivation is at least 8 hours
group E2:duration of fasting and water-deprivation is less than 2 hours
group E4:duration of fasting and water-deprivation is between 2 and 4 hours
group E6:duration of fasting and water-deprivation is between 4 and 6 hours
group E8:duration of fasting and water-deprivation is between 6 and 8 hours

Sponsors

West China Second Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Parturient women =37 gestational weeks; 2. Parturient women=18 years of age; 3. Parturient women whose ASA physical status is I to III; 4. Parturient women weight 50 to 120 kg; 5. Parturient women height =150 cm.

Exclusion criteria

Exclusion criteria: 1) Parturient women who has a history of upper gastrointestinal disorders, including upper gastrointestinal surgery, abnormal anatomy of the upper gastrointestinal tract, peptic ulcer or gastroesophageal reflux disease; 2) Parturient women with pregnancy-induced hypertension; 3) Parturient women with intrahepatic cholestasis of pregnancy; 4) pregnancy associated with diabetes; 5) pregnancy associated with pancreatitis; 6) Parturient women with gastric fundus esophagus varices or cirrhosis of liver.

Design outcomes

Primary

MeasureTime frame
qualitative and quantitative sonographic patterns of the gastric antrum;

Secondary

MeasureTime frame
progestogen level;the tone of the lower esophageal sphincter;the incidence of nausea and vomiting;

Countries

China

Contacts

Public ContactLan Wu

West China Second Hospital, Sichuan University

lancy12@163.com+86 1388091602286

Outcome results

None listed

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