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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03917940
Other study ID # omega 3 in diabetics type 2
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 31, 2019
Est. completion date May 10, 2020

Study information

Verified date November 2023
Source Damanhour University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

study the effect of omega 3 fatty acids on blood glucose, lipids profile, serum Irisin and sirtuin-1 in type 2 diabetic mellitus patients treated with glimepiride.


Description:

1. Approval will be obtained from Research Ethics Committee of Faculty of Pharmacy, Damanhour University 2. All Participants agreed to take part in this clinical study and provide informed consent. Methodology - The study will be conducted in 70 patients who are aged 30-60 years old with type 2 diabetes mellitus for at least 2 years. The patients will be assigned into two groups (Omega - 3/glimepiride, n=35; glimepiride, n=35). - Serum Irisin, sirtuin-1, Hb A1C, Fasting blood sugar (FBS), Lipid profile, Fasting insulin, HOMA-IR and Atherogenic index of plasma (AIP) will be measured at the beginning and after 12 weeks of intervention. - Anthro-pometric parameters including Weight and height to calculate body mass index will be measured at the beginning and after intervention. - past medical history and medication history will be documented. - Each subject in the test group will receive a total dose of 1000 mg of omega-3 fatty acids per day in the form of three capsules along with a glimepiride tablet to be taken once daily, while each subject in the other group will receive glimepiride tablet to be taken once daily for 12 weeks. - Venous blood samples will be obtained from patients at the beginning and after 12 weeks of intervention. - A commercially available enzyme-linked immuno-sorbent assay kits will be used for the measurement of Irisin and sirtuin-1. - The patients will be advised not to change their usual diet, drug regimen and physical activity levels throughout the study.


Recruitment information / eligibility

Status Completed
Enrollment 70
Est. completion date May 10, 2020
Est. primary completion date May 1, 2020
Accepts healthy volunteers No
Gender All
Age group 30 Years to 60 Years
Eligibility Inclusion Criteria: - 70 Adult patients aged 30-60 years old with type 2 diabetes mellitus treated with glimepiride. - glycated hemoglobin percent greater than 7%. - body mass index between 25 and 35 kg/m2. - Patients who are not consuming omega-3 fatty acids, supplements or any pharmaceutical products that may interact with their lipid profile. Exclusion Criteria: - Pregnant or lactating women. - Have gastrointestinal disorders that interfere with the bowel function - patients with severe hepatic, renal, inflammatory and thyroid diseases. - insulin therapy. - Have diabetes complications including micro and macrovascular complications. - Alcoholics and patients with past history of drug abuse.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Omega 3 fatty acids 1000 mg per day + glimepiride 2 mg or 3 mg oral
Omega 3 fatty acids 1000 mg per day oral
Drug:
Glimepiride
glimepiride 2 mg or 3 mg per day oral

Locations

Country Name City State
Egypt Damanhour Medical National Institute Damanhur El-Bahairah

Sponsors (1)

Lead Sponsor Collaborator
Damanhour University

Country where clinical trial is conducted

Egypt, 

References & Publications (2)

Aghasi M, Ghazi-Zahedi S, Koohdani F, Siassi F, Nasli-Esfahani E, Keshavarz A, Qorbani M, Khoshamal H, Salari-Moghaddam A, Sotoudeh G. The effects of green cardamom supplementation on blood glucose, lipids profile, oxidative stress, sirtuin-1 and irisin i — View Citation

Lluis L, Taltavull N, Munoz-Cortes M, Sanchez-Martos V, Romeu M, Giralt M, Molinar-Toribio E, Torres JL, Perez-Jimenez J, Pazos M, Mendez L, Gallardo JM, Medina I, Nogues MR. Protective effect of the omega-3 polyunsaturated fatty acids: Eicosapentaenoic a — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary serum Irisin concentration (ng/ml) Myokines have anti- inflammatory properties three months
Primary serum sirtuin-1 concentration (ng/ml) class III protein deacetylase that is associated with aging, inflammation and CVD three months
Secondary Fasting Blood Sugar Serum Glucose (mg/dl) Three Months
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