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The Effects Of Metformin And Diabinese On Female Sex Hormone Of Type 2 Diabetes Mellitus Patients
[UNIVERSITY OF ILORIN TEACHING HOSPITAL (UITH), ILORIN, KWARA STATE] -
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CHAPTER THREE
3.0 MATERIALS AND METHODS
3.1 STUDY AREA
The study was conducted in the Metropolitan City of Ilorin, Kwara State. Ilorin, the capital city of Kwara State, Nigeria is located on latitude 8o 24’N and 8o 36’N and longitude 4o 10’E and 4o 36’E with an area of about 100Km2 (Kwara State Diary, 1997).
3.2 STUDY POPULATION
The population of this study was centred on patients with type 2 diabetes mellitus on anti-diabetic drugs metformin and diabinese attending University of Ilorin Teaching Hospital (UITH) Ilorin. Also apparently healthy female subject of same age range were recruited from Ilorin metropolis to serve as control. Informed consent was obtained from each participant after proper notification and information on the nature of the research, risk involved, benefits as well as confidentiality.
3.3 INCLUSION CRITERIA
Only subjects that have been quarried for type II diabetes mellitus and on either of these antidiabetes drugs metformin and diabinese for at least one year were recruited for this study.
3.4 EXCLUSION CRITERIA
Subjects that are not type II diabetes mellitus and are not on either of these antidiabetic drugs metformn and diabinese were not recruited for this study.
3.5 SAMPLE SIZE DETERMINATION
The sample size for this study was obtained using the formula described by (Daniel, 1999).
The sample size for this study was determined based on three factors:
1. The estimated prevalence of variable interest from literature review.
2. Confidence interval of 95%.
3. The acceptable margin of error.
The sample size will was then calculated according to the following formula:
n = required sample size
Z = confidence level at 95% (standard value of 1.96)
P = estimated prevalence of type 2 diabetes mellitus in Nigeria (6.8%) (Ogbera and Ekpebegh, 2014).
m = margin of error at 5% (standard value=0.05)
Thus,Therefore, the sample size of the study was increased to one hundred (100) which will encompass sixty (60) subjects with type 2 diabetes mellitus and forty (40) non-diabetic subjects to serve as control.
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