MedPath

Serum D dimer and Procalcitonin Levels at Admission as Predictors of Severity in patients with Acute Pancreatitis

Not yet recruiting
Conditions
Acute pancreatitis, unspecified,
Registration Number
CTRI/2025/04/085322
Lead Sponsor
All India Institute of Medical Sciences Kalyani
Brief Summary

This prospective observational cohort study aims to assessthe predictive value of serum D-dimer and procalcitonin levels at admission indetermining the severity of acute pancreatitis (AP). The study will includeadult patients (18–70 years) presenting within 24 hours of symptom onset. TheRevised Atlanta Classification and Modified Marshall Scoring System will beused to classify AP severity and assess organ dysfunction. Given the associationsof AP with systemic inflammation, sepsis, and microvascular thrombosis,procalcitonin and D-dimer levels may serve as early biomarkers for severityassessment. A total of 62 patients will be recruited, accounting for a 10%dropout rate. Blood samples will be collected at admission for D-dimer andprocalcitonin measurements. Patients will be monitored for up to 8 days oruntil discharge for development of complications, organ failure, and outcomes.Data will be analysed using SPSS, with ROC curve analysis to evaluate thepredictive accuracy of both biomarkers. Multiple regression will identifyindependent predictors of severity and mortality. The study seeks to establishwhether these biomarkers can aid in early risk stratification and guideclinical decision-making in acute pancreatitis.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
62
Inclusion Criteria

Adult patients (18-70 years) with acute pancreatitis presenting within 24 hrs of symptom onset.

Exclusion Criteria
  • 1.Pregnancy.
  • 2.Patients presenting more than 24 hours of symptom onset.
  • 3.Chronic pancreatitis 4.Recurrent pancreatitis 5.Age less than 18 years old or over 70 years old 6.Anticoagulant drug use 7.Cancer 8.Thrombotic diseases 9.Liver cirrhosis 10.Patient on immunosuppressive therapy 11.Refusal to give consent.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
1.To determine if serum D-dimer and procalcitonin levels at the time of admission can predict the severity of acute pancreatitis.Preparation and ethical approval-1-2 months | Data collection- 3 months | Data analysis, reporting and dissemination:1 month
Secondary Outcome Measures
NameTimeMethod
2.To evaluate whether D-dimer and procalcitonin levels are associated with the development of complications and mortality in patients with acute pancreatitis.3.To determine the most reliable predictor between D-dimer and procalcitonin for early risk assessment in Acute Pancreatitis patients.

Trial Locations

Locations (1)

All India Institute of Medical Sciences Kalyani

🇮🇳

Nadia, WEST BENGAL, India

All India Institute of Medical Sciences Kalyani
🇮🇳Nadia, WEST BENGAL, India
Dr Biswajit Naskar
Principal investigator
6290074738
mynameisjit310789@gmail.com

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.