Genetic Diseases
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Participants who are willing to be followed for the 12-week trial period will be included in the study. Sickle cell patients who are not on any lipid lowering drugs will be included in the RCT.
Exclusion criteria
Exclusion criteria: Participants on lipid lowering medication prior to phase II will be excluded. Further, participants with complications (liver/renal conditions) will be excluded due to the high potassium content of cocoa
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The main endpoint will be assessed by the mean changes in lipid profile (HDL-cholesterol and triglycerides | — |
Secondary
| Measure | Time frame |
|---|---|
| The clinically relevant measures will be BMI, blood pressure, waist circumference, hip circumference, waist-to-hip ratio, fasting blood glucose level, C-reactive protein levels, Interleukin-6, TNF-alpha and oxidative stress biomarkers (SOD, CAT). The differences will be compared between intervention and control groups | — |
Countries
Ghana
Contacts
Professor University of Ghana