Trials / Recruiting
RecruitingNCT06380842
Organ Dysfunction Change in Acute Necrotizing Pancreatitis Patients With Sepsis After Open Necrosectomy
Organ Dysfunction Change in Acute Necrotizing Pancreatitis Patients With Sepsis Undergoing Open Necrosectomy
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 200 (estimated)
- Sponsor
- Chunling Jiang · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to characterize organ dysfunction change in acute necrotizing pancreatitis patients with sepsis after open necrosectomy.
Detailed description
Before surgery, study participants will be asked questions about age, gender, education level, etc. Study participants will also be questioned regarding pancreatic symptoms, as measured on the patient-Reported Outcome Scale in Acute Pancreatitis (including, pain, abdominal distention, eating, bowel movements, nausea and vomiting, thirst, and weakness). Organ dysfunction was defined according to the sequential organ failure assessment (SOFA) score. The SOFA score will be measured at preoperative (T1), postoperative day 1 (T2), postoperative day 3 (T3), postoperative day 7, or at hospital discharge, whichever comes first (T4). Following discharge from the hospital, study participants will be contacted at 1 month, 3 months, 6 months, and 1 year after surgery, and asked to complete a survey about their pancreatic symptoms and survival status after surgery.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Necrotizing Pancreatitis patients' organ dysfunction progression | Study the dynamic nature of organ dysfunction |
Timeline
- Start date
- 2024-06-15
- Primary completion
- 2026-12-30
- Completion
- 2026-12-30
- First posted
- 2024-04-24
- Last updated
- 2025-09-23
Locations
1 site across 1 country: China
Source: ClinicalTrials.gov record NCT06380842. Inclusion in this directory is not an endorsement.