Clinical Trials Directory

Trials / Recruiting

RecruitingNCT07433777

Reference Intervals With Indirect Methods in Italy

Status
Recruiting
Phase
Study type
Observational
Enrollment
1,000,000 (estimated)
Sponsor
Centro di Riferimento Oncologico - Aviano · Academic / Other
Sex
All
Age
0 Years – 100 Years
Healthy volunteers
Accepted

Summary

Reference intervals are an essential tool for the clinical interpretation of laboratory test results. Traditionally, these interval are determined using samples from healthy individuals, a process that is resource-intensive, time-consuming, and require the active recruitment of healthy volunteers. In recent years, due to the increasing availability of electronic health record (EHR) databases and the growing number of laboratory tests, it is possible to determine the reference intervals indirectly. This approach relies on the analysis of routine data acquired in clinical laboratories, eliminating the need for active recruiting healthy subjects and significantly reducing costs. Moreover, the method has the potential to eliminate the selection bias of an ultra-healthy population typical of the direct methods. The indirect methods for determining reference intervals have evolved from simple strategies of isolating the healthy population using sample metadata, to sophisticated statistical models that effectively distinguish normal from pathological distributions. One of the advanced techniques, RefineR, has reached an excellent combination of accuracy, robustness, and computational efficiency, outperforming previous methods. It has been implemented as an open-source R package, facilitating its application in real-world settings. In recognition of these advantages, the IFCC (International Federation of Clinical Chemistry and Laboratory Medicine), through its Committee on Reference Intervals and Decision Limits (C-RIDL), has promoted the adoption of indirect methods for determining reference intervals, highlighting the advantages of this strategy, including greater speed, lower costs, and the absence of a need to recruit healthy donors. Furthermore, a recent study has highlighted age-related physiological variations in hemoglobin levels in elderly population. This underscores the need for defining age-specific reference intervals which are currently absent from most laboratory reports, potentially impacting diagnostic accuracy.

Conditions

Timeline

Start date
2025-10-08
Primary completion
2028-06-01
Completion
2028-06-01
First posted
2026-02-25
Last updated
2026-02-25

Locations

24 sites across 1 country: Italy

Source: ClinicalTrials.gov record NCT07433777. Inclusion in this directory is not an endorsement.