Skip to content

Nonspecific anti-inflammatory treatment at early stage for predicted severe acute pancreatitis: a clinical randomized controlled trial

Nonspecific anti-inflammatory treatment at early stage for predicted severe acute pancreatitis: a clinical randomized controlled trial

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-14005059
Enrollment
Unknown
Registered
2014-07-06
Start date
2014-08-01
Completion date
Unknown
Last updated
2018-02-05

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

Conditions

predicted severe acute pancreatitis

Interventions

treatment group:conventional treatment+octreotide+parecoxib/celecoxib
control group:conventional treatment+octreotide

Sponsors

Department of Gastroenterology, West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed as acute pancreatitis having two of the following three features: (1) abdominal pain consistent with acute pancreatitis (acute onset of a persistent, severe, epigastric pain often radiating to the back); (2) serum amylase or lipase activity increased at least three times greater than the upper limit of normal, and 3. characteristic ?ndings of acute pancreatitis on transabdominal ultrasonography and computed tomography (CT)or magnetic resonance imaging (MRI). 2. APACHE II score more than 8; 3. admission within 48h from the onset of symptoms; 4. patients did not receive any NSAIDS, somatostatin and its analogue one month before admission; 5. age older than 18 years old; 6. patients voluntarily signed the informed consent form.

Exclusion criteria

Exclusion criteria: 1. Patients hypersensitive to sulfonamides; 2. women in pregnancy or lactation; 3. patients with severe diseases of heart, lung, brain and kidnery, and patients with other severe diseases of the digestive system, such as cirrhosis, esophageal varices, peptic ulcer, alimentary tract hemorrhage in recent one month, ulcerative colitis, Crohn's disease and malignant tumors; 4. patients with drug abuse, psychinosis et al.

Design outcomes

Primary

MeasureTime frame
incidence of SAP;

Secondary

MeasureTime frame
time of start eating;fluid sequestration in the first 72 hours;plasma somatostatin concentration;fluid input before end-point;duration before end-poin;incidence of long-term complicatio;cost of hospitalization;length of hospital stay;Mortality;incidence of organ failure;OF score;CTSI;SIRS score;APACHE II score;the scores of abdominal pain;Consumption of pethidine;serum C-reaction protein (CRP);serum interleukin-6 (IL-6);serum tumor necrosis factor (IL-6);

Countries

China

Contacts

Public ContactHuang Libin
huanglibin525@163.com+86 18980601869

Outcome results

None listed

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