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The Effectiveness of Date Seed Extract in Controlling Diabetes and Reducing Cardiovascular Risk in Patients With Type 2 Diabetes in Riyadh, Saudi Arabia

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Globally, chronic noncommunicable diseases rank as the leading cause of morbidity and mortality. Diabetes is reaching high epidemic proportions across the globe. The prevalence of diabetes is increasing in Saudi Arabia, with diabetes affecting 14.1% of the population across all age groups and 28% of those over the age of 30. Date seed intake is one of the best-studied patterns. Previous studies findinds showed that the phenolic compounds in date seeds have blood sugar-lowering properties. There is a lack of data on how date seed diets may affect glycaemia control and cardiovascular risk among Saudi Arabian patients with T2DM. Therefore, randomised controlled trials (RCTs) will be conducted to assess the effects of date seeds on glycaemic control and cardiovascular risk among diabetes patients.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• Aged 18 years old and above.

• Diagnosis of Type 2 diabetes.

• Receiving and monitoring diabetes care from diabetes center.

• With stable HbA1c less than 10% (no episode of hypoglycaemia, no hospitalisation, no change in type or dosage of medication use for at least 6 months).

Locations
Other Locations
Malaysia
Dr Zuriati Ibrahim
RECRUITING
Serdang
Contact Information
Primary
Maha Aldaham, Master
maaaldaham8@gmail.com
+60176652101
Backup
Zuriati Ibrahim, PhD
zuriatiib@upm.edu.my
+603-97692464
Time Frame
Start Date: 2024-07-01
Estimated Completion Date: 2025-12-30
Participants
Target number of participants: 160
Treatments
Other: Date Seed Capsule
The intervention group will receive a capsule of date-seed powder. Each person should consume 5 grams (two capsules of date-seed powder) twice daily after meals for three months. Assessments are carried out at the beginning of the study, one month and two months after the intervention (Chan et al., 2013). Participants will be contacted twice a week to ensure that they are adhering to the rules, maintaining their physical activity and clarifying any questions about taking supplements.
No_intervention: Control group: No Intervention
The control group will not receive any capsule ot treatment.
Related Therapeutic Areas
Sponsors
Leads: Universiti Putra Malaysia

This content was sourced from clinicaltrials.gov