Infected pancreatic necrosis and its related septic complications are the major cause of death in patients with acute pancreatitis, therefore prevention of pancreatic infection is of great clinical value in the treatment of AP. Immunosuppression and disorders characterized by decreased HLA-DR expression and unbalanced CD3/CD4+/CD8+ T cells of PBMC are thought to be associated with the development of pancreatic infection. Thymosin alpha 1 has been shown to have immunomodulatory properties and its effects in preventing pancreatic infection was not well studied. To evaluate the effects of TA1 use in the early phase on preventing pancreatic infection, immunomodulation and clinical outcomes in patients with AP,we aimed to design this study.
Study Background \& Rationale: Infected pancreatic necrosis and its related septic complications are the major cause of death in patients with acute pancreatitis1, therefore prevention of pancreatic infection is of great clinical value in the treatment of AP. Immunosuppression and disorders characterized by decreased HLA-DR expression and unbalanced CD3/CD4+/CD8+ T cells of PBMC are thought to be associated with the development of pancreatic infection2, 3. Thymosin alpha 1 has been shown to have immunomodulatory properties and its effects in preventing pancreatic infection was not well studied4. Aim of This Study: To evaluate the effects of TA1 use in the early phase on preventing pancreatic infection, immunomodulation and clinical outcomes in patients with AP. Sample Size Estimation: The prevalence of pancreatic infection was reported to be around 25% in AP episodes. To demonstrate a 40% reduction in the prevalence of pancreatic infection with 80% power at a two-sided alpha level of .05, we projected an estimated sample size of 500 participants. Considering possible 2% withdraw, we plan to randomize 510 patients in total.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
508
In addition to the standard treatment, thymosin therapy will be started after admission: 1.6mg I.H q12h for the first 7 days and 1.6mg I.H, qd for the following 7 days or until discharge.
Placebo inject will be given at the same dose as Thymosin in addition to the standard treatment.
Department of SICU, Research Institute of General Surgery Jinling Hospital, Nanjing, Jiangsu, China
Nanjing, Jiangsu, China
Jinling Hospital
Nanjing, Jiangsu, China
Occurrence of pancreatic infection:
Time frame: during the index admission
The occurrence of new-onset organ failure and new-onset persistent organ failure
(SOFA score for respiration, cardiovascular, or renal system ≥2 ). New-onset is defined as events that occur after randomization and not present 24 hours before randomization
Time frame: during the index admission
In-hospital mortality
Time frame: during the index admission
Bleeding requiring intervention
Time frame: during the index admission
Gastrointestinal perforation or fistula requiring intervention
Time frame: during the index admission
Incidence of pancreatic fistula
Time frame: during the index admission
New receipt of mechanical ventilation/renal replacement therapy /New receipt of vasoactive agents
not applied 24 hours before randomization
Time frame: during the index admission
The requirement for catheter drainage/Number of drainage procedures required
Time frame: during the index admission
The requirement for minimally-invasive debridement/Number of minimally invasive necrosectomy required
Time frame: during the index admission
The requirement for open surgery/Number of open surgery required
Time frame: during the index admission
Length of intensive care unit(ICU) stay/Length of hospital stay
Time frame: during the index admission
SOFA score/ CRP level/ HLA-DR level/ Lymphocyte count
Time frame: on day0, day7, and day14
In-hospital cost.
Time frame: during the index admission
Incidence of infection within 90 days after enrollment
Time frame: 90 days after enrollment
Mortality within 90 days after enrollment
Time frame: 90 days after enrollment
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