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Reference Intervals With Indirect Methods in Italy

Reference Intervals With Indirect Methods in Italy

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07433777
Acronym
REFIND-IT
Enrollment
1000000
Registered
2026-02-25
Start date
2025-10-08
Completion date
2028-06-01
Last updated
2026-02-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Reference Intervals

Brief 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.

Interventions

None listed

Sponsors

Centro di Riferimento Oncologico - Aviano
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
0 Years to 100 Years
Healthy volunteers
Yes

Inclusion criteria

* no one

Exclusion criteria

* no one

Design outcomes

Primary

MeasureTime frame
Define indirect reference intervals for complete blood count (CBC) parameters by analyzing large-scale retrospective routine laboratory data.up to 3 years

Secondary

MeasureTime frameDescription
Assess regional differences by comparing results across 10 Italian regions.up to 3 yearsStatistical heterogeneity will be assessed using Cochran's Q test, and I squared index
Establish age- and sex-specific reference intervalsup to 3 years
Evaluate inter-instrument variations by considering results obtained from different analytical platforms.up to 3 yearsStatistical heterogeneity will be assessed using Cochran's Q test, and I squared index

Countries

Italy

Contacts

CONTACTFabio Del Ben
fabio.delben@cro.it0434659101

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026