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Survey of Thai-Muslim Health Status

M

Mahidol University

Status

Completed

Conditions

Hypertension
Diabetes
Hyperlipidemia

Treatments

Other: No intervention

Study type

Observational

Funder types

Other

Identifiers

NCT00701454
INMU-2006-01

Details and patient eligibility

About

The purpose of this study was to determine the prevalence and risk factors of diabetes, hypertension, hyperlipidemia among Thai muslim population aged 35-75 years.

Full description

This was a cross-sectional study conducted in Bangkok and surrounding provinces. Approximately 1500 participants were enrolled. Study staff interviewed participants on basic demographic data, health status, physical activities, food frequency and 24-hour recall. Anthropometry (body weight, height, hip and waist circumference) and physical assessment (blood pressure)were measured. Ten milliliters of venous blood was drawn by venipuncture after a 12 h overnight fast for determination of fasting plasma glucose (FPG) and blood lipid concentrations (total cholesterol, triglyceride, and HDL-cholesterol). FPG was measured by the enzymatic colorimetric method with glucose oxidase.21 Total cholesterol was determined by the cholesterol oxidase method and serum triglycerides concentration was determined by standardized enzymatic procedures using glycerol phosphate oxidase assay.22, 23 HDL- cholesterol was measured by enzymatic assays.24 LDL cholesterol was calculated according to the method of Friedwald et al.25 All samples were analyzed when internal quality control met the acceptable criteria. Intra-and inter-assay CVs were 2.01% and 3.01% for FPG, 1.87% and 4.24% for total cholesterol, 0.93% and 11.6% for triacylglycerols, and 0.99% and 1.49% for HDL cholesterol, respectively.

Enrollment

1,488 patients

Sex

All

Ages

35 to 95 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • 35 y and older muslim
  • free from severe communicable diseases and mental disorders

Exclusion criteria

  • not able to complete the interviews or obtain blood samples for analysis

Trial design

1,488 participants in 1 patient group

1
Description:
Healthy participants (physically and mentally).
Treatment:
Other: No intervention

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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