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The effect of initiation of nasojejunum tube feeding on different time-points on infection and organ failure in severe acute pancreatitis

The effect of initiation of nasojejunum tube feeding on different time-points on infection and organ failure in severe acute pancreatitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16009092
Enrollment
Unknown
Registered
2016-08-25
Start date
2016-09-30
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

acute pancreatitis

Interventions

NTF within 72h:naso-jejunum tube feeding
NTF after 72h:naso-jejunum tube feeding

Sponsors

Chengdu Military General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. All cases should be in accordance with the SAP diagnostic criteria for classification of acute pancreatitis in Atlanta (2012); 2. Patients aged from 18 to 65 years old; 3. The onset time is less than 72 hours till the time of radomization, admission without nutritional support treatment; 4. Patients APACHE II score is greater than or equal to eight pointsor C-reactive protein is greater than or equal to 150mg/dlor BalthazarCT score is greater than or equal to four points within 48 hours after onset; 5. Patients and their family members volunteered to the object of the observation and fill in the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with malignant tumor, chronic organ dysfunction and other severe diseases were excluded; 2. Patients with gastrointestinal bleeding, intestinal obstruction and other digestive tract diseases were excluded; 3. Exclusion of pregnancy SAPtraumatic SAP patients, post-ERCP AP; 4. Exclusion of SAP patients who were unable to be placed in the jejunum nutrition tube, or who were unable to tolerate long-term placement of the jejunum nutrition tube; 5. Patients with open abdominal surgery before admission and after admission were excluded; 6. Gastric retention presenting from clinical symptom, physical signs or abdominal CT examination; 7. Patients with drug abuse, psychinosis; 8. Allergy to the EN formula; 9. the intra-abdominal pressure is greater than or equal to 15mmHg; 10. hemodynamic instability.

Design outcomes

Primary

MeasureTime frame
peri-pancreatic infection;Ascites bacterial culture positive;number of organ failure;

Secondary

MeasureTime frame
DAO;D-lactate;endotoxin;PCT;TNF-alfa;IL-1;IL-6;MTL;VIP;prealbumin;RBP;transferrin;hemoglobin;AC;TSF;AMC;the power of gripping;length of ICU stay;hospital stay;fee;intra-abdominal pressure;bowel sound;time interval from onset to fart;time interval from EN start to target;diarrhea;conspitation;hemorrhage of digestive tract;nausea;vomit;obstruction;dislodging;Abdominal pain score;

Countries

China

Contacts

Public ContactLi-Jun Tang

Chengdu Military General Hospital

13258198900@163.com+86 028-86570479

Outcome results

None listed

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