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The samples collected from the participants will be estimated by manual and automated method to measure the ESR values and the main outcome of the study will compare the accuracy of both the methods.

Bridging tradition and innovation: A study of ESR measurement methods - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2025/07/090308
Enrollment
200
Registered
2025-07-07
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Health Condition 1: R65- Symptoms and signs specifically associated with systemic inflammation and infection

Interventions

Intervention1: Nil: Nil

Sponsors

MAMC Lok Nayak Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: All EDTA blood samples received from OPD and IPD for routine investigations

Exclusion criteria

Exclusion criteria: 1. Blood samples which are hemolysed, lipemic and clotted. 2. Inadequate quantity of blood sample.

Design outcomes

Primary

MeasureTime frame
Validation of automated ESR measurement method.Timepoint: 8 weeks—

Secondary

MeasureTime frame
NILTimepoint: NA—

Countries

India

Contacts

Public ContactDr Rashmi Jain Gupta

Lok Nayak Hospital

drrashmijaingupta@gmail.com9873617571

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026