Clinical Trials Directory

Trials / Completed

CompletedNCT04820465

Anemia in Older Adults

Identification of the Main Causes of Anemia in Older Adults

Status
Completed
Phase
Study type
Observational
Enrollment
829 (actual)
Sponsor
Instituto Nacional de Salud Publica, Mexico · Academic / Other
Sex
All
Age
60 Years
Healthy volunteers
Accepted

Summary

A cross-sectional study with 829 older Mexican adults were recruited from July to September 2015, from four localities in the southern region of México. Older adults were interviewed at their homes and a fasting blood sample was obtained for analysis of micronutrient status (iron deficiency, vitamin B12 deficiency, folate deficiency, vitamin A deficiency and biomarkers of inflammation). The aim of the study was to identify the main causes of anemia in older adults with higher rates of anemia according to the recent data of the Mexican National Health and Nutrition Survey.

Detailed description

A survey with cross-sectional design was applied in 829 older Mexican adults, recruited during the period July to September 2015, from four localities in the southern region of México: including Champotón, Campeche, Mérida, and Valladolid. Older adults were interviewed at their homes to collect nutrition, health, cognitive and dietary information. Anthropometric measures and functionallity tests were also collected. A finger prick capillary blood sample was collected to measure hemoblobin in situ using HemoCue. Anemia was defined according to WHO criteria. A fasting venous blood sample was collected in 803 older adults. Serum was separated and frozen at -20°C to measure ferritin, retinol, vitamin B12, folate, iron, soluble transferrin receptor, C-reactive protein, interleukin 6, alpha glycoprotein 1, hepcidin, erythropoietin in the laboratory of nutrition of the National Institute of Public Health. The study protocol was approved by Research, Biosecurity and Ethics Committees of the National Institute of Public Health. Participants received a detailed explanation of the study procedures and signed an informed consent form prior to data collection.

Conditions

Interventions

TypeNameDescription
OTHERNon available due to cross-sectional study designNon available since this study (survey) has a cross-sectional design

Timeline

Start date
2015-07-01
Primary completion
2015-09-01
Completion
2015-09-01
First posted
2021-03-29
Last updated
2021-03-29

Source: ClinicalTrials.gov record NCT04820465. Inclusion in this directory is not an endorsement.