跳至主要内容
临床试验/NCT06867120
NCT06867120招募中不适用

Bowel Sound in Predicting the Severity of Acute Pancreatitis: Protocol of a Prospective, Multi-center Study

Peking Union Medical College Hospital1 个研究点 分布在 1 个国家目标入组 352 人开始时间: 2024年4月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
352
试验地点
1
主要终点
Number of participants with severe acute pancreatitis (SAP) during hospitalization within 7 days after enrollment.

研究概览

简要总结

Introduction: Acute pancreatitis (AP) is a common condition, with 20% of cases progressing to severe acute pancreatitis (SAP), which is associated with a poor prognosis. Early identification of patients likely to progress to SAP is crucial for timely intervention. This study aims to use bowel sound monitoring to predict early progression to SAP in AP patients.

Methods and analysis: This study is a prospective, multi-center prognostic study . Investigators will consecutively recruit newly diagnosed acute pancreatitis (AP) patients at emergency departments across three centers from December 2023. Upon enrollment, each patient will undergo continuous bowel sound monitoring for at least 48 hours using standardized equipment and procedures. The primary outcome is the occurrence of SAP during hospitalization. Collected bowel sound data will be analyzed by an unsupervised automated algorithm to estimate a bowel sound activity index, which serves as the main diagnostic indicator for SAP. This process will be fully blinded to patients' SAP status. Investigators will calculate the ROC curve and area under the curve (AUC) for the bowel sound activity index's ability to diagnose SAP. Additionally, this study will perform exploratory analyses on differences in gut microbiota and serum intestinal permeability markers (diamine oxidase, D-lactic acid, and bacterial endotoxin) between patients with and without SAP. Investigators will also assess whether bowel sound monitoring can reflect these inter-group differences.

Strengths and limitations of the study:

  1. Our research aims to monitor bowel sounds in real-time and dynamically, providing an objective tool for monitoring intestinal activity in AP patients.
  2. Our research might offer an objective tool to evaluate bowel sounds, aiding in assessing AP patients' intestinal function and complementing existing score systems like the modified Marshall score.
  3. By detecting bowel sounds in the early stage of AP, investigators could better monitor intestinal function, which might aid in predicting the prognosis of AP patients.
  4. Our monitoring system's main limitation is its difficulty in pinpointing bowel sound changes in specific intestinal segments due to its detection across the entire abdomen.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Aged between 18 and 85 years old.
  • •Meet the diagnostic criteria for AP, at least two of the following three: (a) characteristic abdominal pain; (b) serum amylase and lipase levels are greater than three times the upper limit of normal; (c) abdominal images with typical manifestations of AP.
  • •AP patients within 48 hours of onset.
  • •The patient or family members understand the study protocol and sign the informed consent form.

排除标准

  • •The patients who fulfill any of the following criteria will be excluded:
  • •Patients with serious conditions requiring surgery and abdominal lavage.
  • •Pregnant women.
  • •The patients with muscle and nerve disorders, chronic pancreatitis, inflammatory bowel disease, cancer, and irritable bowel syndrome.
  • •The patients with severe digestive, respiratory, cardiovascular, hematological, endocrine, psychiatric, and infectious diseases.
  • •The patients have a history of abdominal surgery (except appendectomy or cholecystectomy).
  • •Allergic to silicone, polycarbonate materials or medical plaster. The intake of antibiotic, probiotics, and Chinese herbal medicine will be recorded before the collection of the swabs and will not be considered as exclusion criteria.

研究组 & 干预措施

Observational Cohort

结局指标

主要结局

Number of participants with severe acute pancreatitis (SAP) during hospitalization within 7 days after enrollment.

时间窗: Within 7 days after enrollment.

SAP was defined as AP patients with persistent organ failure according to the revised Atlanta classification.

次要结局

  • Number of participants with in-hospital mortality.(Within 30 days after enrollment.)
  • Number of participants with 30-day mortality.(Within 30 days after enrollment.)
  • Length of hospital stay.(Within 30 days after enrollment.)
  • Number of participants with organ failure.(Within 30 days after enrollment.)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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