Pure Global AI
NCT06378853Completed

Risk Factors of Postoperative Complications and Survival Rate in Pancreatic Ductal Adenocarcinoma Patients

Risk Factors of Postoperative Complications and Survival Rate in Pancreatic Ductal Adenocarcinoma Patients Based on Body Compositions Measured by 3D CT Scan and Hematological Indicators
Jinling Hospital, ChinaClinicalTrials.govother
Study focus
Disease/Condition
Pancreatic Cancer
Drug/Device/Intervention
no intervention
Study type
Observational
Intervention type
other
Sponsor & location
Primary sponsor
Jinling Hospital, China
Location
Nanjing, China
Timeline & enrollment
Phase
N/A
Start date
Jan 01, 2019
End date
Feb 28, 2024
Enrollment
548 participants
Primary outcome

complications,overall survival,risk factors

Summary

By evaluating the nutritional status of patients with pancreatic ductal adenocarcinoma (PDAC)
 admitted to Jinling Hospital, collecting relevant clinical data. we aim to conduct
 correlation analysis with patient clinical information, such as survival time,
 hospitalization time, nutritional status, hematological indicators, etc., in order to reveal
 the prognostic factors for overall survival and postoperative complications of PDAC patients.

ICD-10 classifications
Malignant neoplasm of pancreasMalignant neoplasm: Pancreas, unspecifiedMalignant neoplasm: Head of pancreasMalignant neoplasm: Tail of pancreasMalignant neoplasm: Other parts of pancreas
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06378853
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06378853 through Pure Global AI's free database. This phase not specified trial is sponsored by Jinling Hospital, China and is currently Completed. The study focuses on Pancreatic Cancer. Target enrollment is 548 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.