Clinical Trials Directory

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

TypeNameDescription
OTHERNecrotizing Pancreatitis patients' organ dysfunction progressionStudy 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.