Establishing blood test reference intervals for pregnant women in Vietnam
Establishment of Reference Intervals of Complete Blood Count and Coagulation Tests in Pregnant Women at Hung Vuong Hospital
This study is trying to find out the normal blood test ranges for pregnant women in Vietnam to help doctors provide better care during pregnancy.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 810 (estimated) |
| Ages | 18 Years and up |
| Sex | Female |
| Sponsor | Hung Vuong Hospital Academic / other |
| Locations | 1 site (Ho Chi Minh) |
| Trial ID | NCT05929326 on ClinicalTrials.gov |
What this trial studies
This observational study aims to establish reference intervals for complete blood count and coagulation tests specifically for pregnant women at Hung Vuong Hospital in Vietnam. The study will involve a cross-sectional design, collecting blood samples from pregnant women without any underlying health conditions across all three trimesters. A total of 774 participants will be recruited, and their blood samples will be analyzed using advanced hematology and coagulation analyzers to determine the central 95% interval of test results. Statistical analysis will be performed to compare reference intervals across trimesters to ensure accurate clinical guidelines for this population.
Who should consider this trial
Good fit: Ideal candidates for this study are pregnant women with singleton pregnancies and no significant medical history.
Not a fit: Patients with conditions such as hypertension, diabetes, or any current infections will not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide essential reference intervals for blood tests in pregnant women, improving prenatal care and health outcomes.
How similar studies have performed: While many studies have established reference intervals globally, this specific approach in Vietnam is novel and has not been previously tested.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Singleton Pregnancy Exclusion Criteria: * Hypertension, Diabetes, Preeclampsia, Gestational Diabetes, Hemoglobinopathy, Current Infection, Positive Screening for Treponema pallidum, Hepatitis B Virus, HIV, usage of anticoagulant drug.
Where this trial is running
Ho Chi Minh
- Hung Vuong Hospital — Ho Chi Minh, Vietnam (Recruiting)
Study contacts
- Study coordinator: Tri Bao Nguyen, Doctor
- Email: baotribvhv09@yahoo.com.vn
- Phone: +8402838558532
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.