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Serial assessment of gastric contents using MRI

Evaluation of the validity of preoperative oral intake restriction for intravenous sedation using magnetic resonance imaging (MRI)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1042240046
Enrollment
36
Registered
2024-06-14
Start date
2024-06-14
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Healthy adult: Evaluate gastric emptying time after oral intake of solid food

Interventions

Group A: MRI scan after ingestion of solid meal according to Japanese diet (888 kcal) Group B: MRI scan after ingestion of solid foods according to Western diet (883 kcal) Group C: MRI scan after inge

Sponsors

Goto Takashi
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1) Healthy ( ASA-PS class 1 or 2 ) 2) Gender: male 3) BMI: 18.5 - 30 kg/m2 4) Age at consent: between 18 and 45 years old 5) After receiving sufficient explanation about participation in this study and with full understanding, the subject must give his/her free and voluntary consent in writing and sign a consent form

Exclusion criteria

Exclusion criteria: 1) Those with a history of allergy to the test food 2) Those with a factor of delayed gastric contents evacuation (1) Those with abnormal gastrointestinal motility (2) Those diagnosed with any of the following diseases known to be associated with abnormal gastrointestinal motility. Gastric insufficiency paralysis, amyloidosis, neuromuscular disease (including Parkinson's disease), collagen vascular disease, alcoholism, uremia, malnutrition, untreated hypothyroidism (3) Morbidly obese with BMI > 30 kg/m2 (4) History of active or severe peptic ulcer (5) Diabetes mellitus (6) Known history of gastrointestinal surgery (7) Esophageal hiatal hernia (8) Signs of gastroesophageal reflux esophagitis (9) Patients who have taken medications that affect gastric acid secretion or evacuation within 48 hours of study participation 3) Inability to perform MRI (1) Wearing implants, metal or non-removable braces on the body (2) Claustrophobia (3) Patients who have a phobia of claustrophobia (4) Patients with congestive heart failure (5) Patients who have taken antimicrobial agents within 30 days prior to the study date (6) Other patients judged by the principal investigator or subinvestigator to be inappropriate as subjects for the study

Design outcomes

Primary

MeasureTime frame
changes in gastric contents over time

Secondary

MeasureTime frame
blood sugar level

Contacts

Public ContactRie Hayashi

Asahi University Medical and Dental Center

minionrie@outlook.jp+81-58-329-1479

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026