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A multi-center, cross-sectional observational study on the nutritional status and body composition of adult IBD patients

A multi-center, cross-sectional observational study on the nutritional status and body composition of adult IBD patients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000035720
Enrollment
Unknown
Registered
2020-08-16
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-08-17

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

Conditions

Inflammation Bowel Disease (IBD)

Interventions

case series:Nil

Sponsors

General Hospital of Eastern Theater Command
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Aged >18 years; 2. Combining clinical, hematological indicators, endoscopic and pathological examinations to diagnose IBD; 3. Admission time < 48 hours; 4. Agree to participate in this study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Emergency surgery for intestinal fistula or abdominal abscess; 2. Unstable vital signs or unstable hemodynamics (for example, systolic blood pressure 3mg/dl or tissue biopsy diagnosed as liver cirrhosis, hepatic encephalopathy, portal hypertension with history of gastrointestinal bleeding, etc.); 7. Severe renal insufficiency (creatinine value is 2 times higher than the upper limit of normal); 8. Severe metabolic diseases (such as metabolic syndrome, hyperthyroidism, etc.); 9. Patients whose burn area exceeds 20% of body surface area; 10. Immune deficiency, autoimmune disease or receiving immunosuppressive treatment for other diseases except IBD (such as organ transplantation, etc.); 11. Those who are not suitable for body composition analysis: those who have a pacemaker installed and cannot perform bioelectrical impedance measurement; those who have too thick ankle stratum corneum to measure body composition data; those who are unconscious and cannot cooperate with the measurement; there is metal in the body Substances such as internal fixators, artificial joints, etc. may affect the measurement results. 12. Patients who have been selected for other clinical studies or have been selected for this study.

Design outcomes

Primary

MeasureTime frame
ASMI;

Secondary

MeasureTime frame
body muscle cotent;BMI(body weight index);

Countries

China

Contacts

Public ContactXinying Wang

General Hospital of Eastern Theater Command

wangxinying@nju.edu.cn+86 13913028866

Outcome results

None listed

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