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Reference Intervals of Complete Blood Count and Coagulation Tests in Pregnant Women at Hung Vuong Hospital

NCT05929326 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 879

Last updated 2025-06-04

Study results available
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Summary

Rationale: Pregnancy has major effects on physiology in women. There have been many studies that established reference intervals but none was done in Vietnam. The recommendation by CLSI C28-A3 is that if possible, each laboratory establishes its own reference intervals.

Objective: To establish the reference intervals of complete blood count parameters and Prothrombin time (PT), activated partial thromboplastin time (aPTT), fibrinogen.

Study design: This is a cross-sectional study.

Study population: Pregnant women with no history of disease and normal clinical findings.

Conditions

  • Pregnancy Related

Interventions

DIAGNOSTIC_TEST

complete blood count, PT, aPTT, fibrinogen tests

Pregnant women who are eligible for the study will have their blood collected to run complete blood count, PT, aPTT, fibrinogen tests

Sponsors & Collaborators

  • MITALAB COMPANY LIMITED

    collaborator UNKNOWN

  • Hung Vuong Hospital

    lead OTHER

Principal Investigators

  • Huan N Pham, Doctor · Hung Vuong Hospital

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-06-09
Primary Completion
2023-08-21
Completion
2023-08-21

Countries

  • Vietnam

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05929326 on ClinicalTrials.gov