- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05479799
Prevalence and Determinants of Anemia During the Third Trimester of Pregnancy
This cross-sectional study was conducted on 383 pregnant women who attended the antenatal care clinic during their third trimester at Beni-Suef University Hospital.
A proper history was taken from each participant. All women were subjected to routine antenatal care, including physical examinations, ultrasound examinations, and routine laboratory tests.
According to WHO criteria, anemia was diagnosed with a hemoglobin level of less than 11.0 g/dl. Anemia was further divided into three degrees; mild with hemoglobin level 10-10.9 g/dl, moderate with hemoglobin level 7-9.9 g/dl, and severe with hemoglobin level < 7.0 g/dl.
Study Overview
Status
Conditions
Detailed Description
This cross-sectional study was conducted on 383 pregnant women who attended the antenatal care clinic during their third trimester at Beni-Suef University Hospital.
A proper history was taken from each participant regarding age, educational level, residency (urban or rural), occupation, family income, frequency of antenatal visits, obstetric history, medical history, and surgical history. Nutritional history is taken to detect the frequency intake of meat/month, chicken/week, fish/week, fruits/week, vegetables/week, and tea/day. History of iron supplements intake was taken. All women were subjected to routine antenatal care, including a physical examination (e.g., measuring blood pressure), ultrasound, and umbilical artery Doppler examination. A blood sample was taken from each enrolled woman for standard laboratory tests such as complete blood picture, blood group, RH type, and blood sugar test if there is a risk. A urine sample was taken for urine analysis. Blood from each participant was drawn from the cubital vein into appropriate blood collection tubes using vacuum tube needles (Becton Dickinson Medical Devices Co. Ltd., Franklin Lakes, USA). K2EDTA tubes were used for CBC. Samples were transported and tested within 4 hours after collection. Measured CBC parameters included RBC, HGB, HCT, mean corpuscular volume (MCV), mean corpuscular hemoglobin (MCH), MCH concentration (MCHC), platelet count (PLT), WBC, and WBC differentials, including percentages and absolute counts of neutrophils (NEUT% and NEUT), lymphocytes (LYM% and LYM), monocytes (MONO% and MONO), basophils (BASO% and BASO), and eosinophils (EO% and EO).
According to WHO criteria, anemia was diagnosed with a hemoglobin level of less than 11.0 g/dl. Anemia was further divided into three degrees; mild with hemoglobin level 10-10.9 g/dl, moderate with hemoglobin level 7-9.9 g/dl, and severe with hemoglobin level < 7.0 g/dl.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Banī Suwayf, Egypt
- Beni-Suef University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- pregnant women during their third trimester
Exclusion Criteria:
- Women with chronic medical illness
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Cross-Sectional
Cohorts and Interventions
Group / Cohort |
|---|
|
Anemia group
anemia was diagnosed with a hemoglobin level of less than 11.0 g/dl
|
|
Non-anemia group
Normal hemoglobin was diagnosed with a hemoglobin level of more than 11.0 g/dl
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of participants with the prevalence of anemia in the third trimester of pregnancy
Time Frame: through study completion (3-6 months)
|
Number of participants with the prevalence of anemia in the third trimester of pregnancy in a specific geographical area (Beni-Suef University Hospital as a tertiary referral center)
|
through study completion (3-6 months)
|
Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- anemia in pregnancy: Beni-Suef
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Anemia of Pregnancy
-
Universitas PadjadjaranCompleted
-
The University of Texas Medical Branch, GalvestonTerminatedPregnancy Related | Iron Deficiency Anemia of PregnancyUnited States
-
Thomas Jefferson UniversityAuerbach Hematology and OncologyRecruitingPregnancy Related | Anemia, Iron Deficiency | Anemia of PregnancyUnited States
-
University of ArizonaAMAG Pharmaceuticals, Inc.CompletedIron Deficiency Anemia of PregnancyUnited States
-
UConn HealthCompleted
-
Thomas Jefferson UniversityJawaharlal Nehru Medical CollegeCompletedIron Deficiency Anemia | Child Development | Iron Deficiency Anemia of Pregnancy | Iron Deficiency Anemia Treatment | Neurodevelopmental Disorder of Foetus | Fetal Neurodevelopmental DisorderIndia
-
Orchidia pharmaceutical IndustriesMARS-GlobalNot yet recruitingIron Deficiency Anemia | Anemia of Pregnancy
-
Boston University Charles River CampusLata Medical Research FoundationCompletedAnemia | Anemia, Iron Deficiency | Anemia of PregnancyIndia
-
Assiut UniversityCompletedAnemia of PregnancyEgypt
-
Cairo UniversityCompleted