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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01958034
Other study ID # 2013-06-05
Secondary ID
Status Completed
Phase Phase 4
First received September 27, 2013
Last updated October 9, 2016
Start date February 2014
Est. completion date November 2015

Study information

Verified date October 2016
Source Region Örebro County
Contact n/a
Is FDA regulated No
Health authority Sweden: Regional Ethical Review Board
Study type Interventional

Clinical Trial Summary

In a double blinded, randomized, clinical trial of patients suffering from STEMI (ST-segment elevation myocardial infarction) or non-STEMI (non-ST-segment elevation myocardial infarction)compare the effect of 3 months of dietary supplement with bilberry extract on a range of parameters with prognostic importance in cardiovascular disease: lipids, inflammation, oxidative stress and heart function.

Following inclusion of 8 individuals and as of February 12, 2014: Due to intolerance to "bilberry placebo powder" we have amended to the protocoll that the trial design is changed from blinded to open and that the bilberry arm of the trial carries on in an open design and that the control group will receive no dietary supplement.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date November 2015
Est. primary completion date November 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Patients with a diagnosis of STEMI as defined by chest pain suggestive for myocardial ischemia for at least 30 minutes before hospital admission, time from onset of symptoms of less than 24 hours, and an ECG with new ST-segment elevation in two or more contiguous leads of =0.2 mV in leads V2-V3 and/or =0.1 mV in other leads or a probable new-onset left bundle branch block.

- Patients with a diagnosis of non-STEMI as defined by a combination of; onset of symptoms such as central chest pain or an aggravated angina pectoris, with or without an ECG change with ST-segment lowering or an inverted T-wave, and at least two values with levels of troponin-T or troponin-I above the established margin of an MI.

Exclusion Criteria:

- Need for emergency coronary artery bypass grafting

- Inability to provide informed consent

- Age below 18 years

- Previous randomization in the BEAR SMART trial

- A daily intake, or the intent to start a daily intake of bilberries in some form (fresh berries, bilberry powder, bilberrysoup etc)

Exclusion Criteria:

- Need for emergency coronary artery bypass grafting

- Inability to provide informed consent

- Age below 18 years

- Previous randomization in the BEAR SMART trial

- A daily intake, or the intent to start a daily intake of bilberries in some form (fresh berries, bilberry powder, bilberrysoup etc)

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
Bilberry extract


Locations

Country Name City State
Sweden Department of Cardiology, Orebro University Hospital Orebro

Sponsors (1)

Lead Sponsor Collaborator
Region Örebro County

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary 6 minutes walk test The effect of intervention on a standardized physical challenge - the 6 minutes walk test 2 months No
Secondary C-reactive protein The effect of intervention on the inflammatory marker CRPö Baseline and 2 months No
Secondary Inflammatory markers and markers of heart function The effect of intervention on markers of inflammation: IL-6 (interleukin 6), TNF-a (tumor necrosis factor a), INF-? (interferon ?), markers of oxidative stress: oxidized LDL, carbonylated proteins, 2-OHDG, H2O2, hexanoyl L lysine, nitrogen oxide synthase (NOS), markers of myocardial damage and heart failure: BNP (brain natriuretic peptide) and troponin I, markers of endothelial function: VEGF (vascular endothelial growth factor), 8-isoprostane, E-selectin, measures of plasma lipids; total cholesterol, LDL-cholesterol, TGA (triacylglycerides), and measures of patient compliance and biological effect of bilberry supplementation: quercetin, Baseline and 2 months No
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