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RECRUITING
NCT06422650
PHASE2

Effect of Nigella Sativa in Atorvastatin Treated Hyperlipidaemia

Sponsor: Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh

View on ClinicalTrials.gov

Summary

This study will be 8 weeks randomized, double-blind, placebo-controlled trail to assess the effect of Nigella Sativa in 84 Hyperlipidaemic patients. Participants will be assessed at baseline and after 8 weeks of intervention. Subjects will be randomized to receive either Nigella Sativa 500 mg capsule daily or placebo capsule identical to Nigella Sativa twice daily for 8 weeks. Evaluation of lipid profile, SGPT, S.Creatinine will be before and after 8 weeks of intervention. Nigella Sativa related adverse events will be identified. Study outcome will establish safety and efficacy of Nigella Sativa in atorvastatin treated hyperlipidaemic patients

Official title: Effect of Nigella Sativa on Blood Lipids as an add-on Therapy in Atorvastatin Treated Hyperlipidaemic Patients. A Randomized Controlled Trial

Key Details

Gender

All

Age Range

18 Years - 75 Years

Study Type

INTERVENTIONAL

Enrollment

84

Start Date

2023-08-24

Completion Date

2024-08-31

Last Updated

2024-05-21

Healthy Volunteers

Yes

Conditions

Interventions

DRUG

Nigella Sativa capsule 500mg

Nigella Sativa capsule 500mg twice daily for 8 weeks

DRUG

Placebo

Oral placebo identical to astaxanthin

Locations (1)

BSMMU

Dhaka, Bangladesh