ovel Test Method for Non-Obstructive Mesenteric Ischemia (NOMI)
- Conditions
- Patients admitted to the esophago-gastrointestinal surgical ward or ICU (regardless of disease)
- Registration Number
- JPRN-jRCTs032230527
- Lead Sponsor
- Ohira Gaku
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 24
Patients with suspected NOMI: Patients suspected of developing NOMI
1) Patients who have given consent to participate in this study, either by themselves or by a surrogate
2) Patients who are 20 years of age or older
3) Patients who have consulted with the Department of Esophagology and Gastroenterology, Chiba University Hospital
4) Patients with abdominal findings such as abdominal pain, abdominal distention, and any of the following
(1) Worsening or new onset of circulatory failure
(2) Prolonged elevation of Lactate in blood
Non-NOMI patients: Control patients without organ failure
1) Patients who are 20 years old or older.
2) Patients who were admitted to the Department of Esophago-Gastrointestinal Surgery, Chiba University Hospital by walking in for scheduled surgery.
3) Patients who have obtained consent for participation in this study from themselves or their significant others.
1) Patients who are unable to perform ultrasound examinations due to inability to carry the equipment to the bedside.
2) Patients who are pregnant, possibly pregnant, within 28 days postpartum, or breastfeeding
3) Patients who are deemed by the physician to be inappropriate for the safe conduct of this study
1) Patients with abdominal symptoms on admission
2) Patients who cannot walk independently
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Tolerability of new testing methods
- Secondary Outcome Measures
Name Time Method Detection rate in each organ