Circulatory System Musculoskeletal Diseases Nutritional, Metabolic, Endocrine Kidney Disease Cardiology Orthopaedics
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients with confirmed diagnosis of type 2 diabetes mellitus. 2. Patients on oral hypoglycaemic therapy for over six (6) months. 3. Patients with poor glycaemic and poor blood pressure and/ or poor lipid control. 4. Patients who the Consultant Endocrinologist of the hospital consented to their entry into the trial. 5. Patients who consented to the study by giving oral consent.
Exclusion criteria
Exclusion criteria: 1. Patients with secondary forms of hypertension. 2. Patients who were pregnant 3. Patients resident outside urban settlements within the study site. 4. Patients without mobile phone numbers. 5. Patients on insulin therapy.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Glycated Haemoglobin A1c (HbA1c) measured using the In2it Analyzer model 501122R.1;Drug therapy problems were identified using a stepwise approach and a specially designed data collection sheet.;Health-related quality of life is measured using the short form – 12 (SF-12) questionnaire and evaluated using the online SF-12 Health Survey Scoring Demonstration. | — |
Secondary
| Measure | Time frame |
|---|---|
| Fasting Blood Sugar (FBS), measured using the Cardio-Check PA Analyzer model CE0197;Lipid profile (total cholesterol, low-density lipoprotein cholesterol, triglycerides, and high-density lipoprotein cholesterol) was measured using the Cardio-Check PA analyzer model CE0197.;10–year risk of coronary heart disease (CHD) score evaluated using online health calculators. This calculator takes account of the patient’s age, gender, smoking status, blood pressure, total cholesterol, and HDL-C.;Body mass index (BMI), is evaluated using online health calculators.;Systemic blood pressure, measured using Omron M6 Comfort Automatic Blood Pressure Monitor model HEM-7321-E;Improvement in the quality of prescribing done by the process of medication review. Here the research pharmacist discusses with the doctors regarding drug therapy and if necessary, treatment modifications were recommended as a follow-up to the pharmaceutical care plan, e.g. more intensive management of hypertension, hyperglycemia, dyslipidemia, or simplification of dosage regimen if deemed appropriate, taking account of the latest treatment guidelines. During the medication review, all drug therapy problems identified that required the attention of the physician or prescriber were presented to the consultant endocrinologist for appropriate management. | — |
Countries
Nigeria
Contacts
Medical Director