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Effects of Chocolate in Patients With Chronic Heart Failure

Effects of Swiss Dark Chocolate on Endothelial and Baroreceptor Function and Markers of Inflammation in Patients With Chronic Heart Failure

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00538941
Enrollment
22
Registered
2007-10-03
Start date
2005-11-30
Completion date
2009-10-31
Last updated
2009-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Heart Failure

Keywords

chocolate,, heart failure,, endothelial function,, platelet adhesion,, oxidative stress,, baroreceptor function,

Brief summary

The aim of the present study is to investigate whether in patients with chronic heart failure endothelial dysfunction and baroreceptor function is altered by ingestion of a flavonoid-rich dark chocolate in comparison to placebo chocolate (Nestlé Placebo Chocolate) on top of standard medication. Moreover, we will evaluate the effect of chocolate on oxidative stress, platelet adhesion as well as systemic inflammatory response such as C-reactive protein and pro-inflammatory cytokines in patients with chronic heart failure.

Interventions

DIETARY_SUPPLEMENTNestlé Noir intense 40 grx2

daily intake of 40gr chocolate (Nestlé Noir intense or Nestlé Placebo Chocolate) in the morning and 40gr chocolate in the evening.

DIETARY_SUPPLEMENTNestlé Placebo Chocolate 40 grx2

Nestlé Placebo Chocolate 40 gr in the morning and 40gr chocolate in the evening.

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
30 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

1. Heart failure ( NYHA ≥II, LVEF\<50%, independent of aetiology) 2. Nonsmokers 3. Age: 30-80 4. Written obtained informed consent

Exclusion criteria

1. Decompensated Heart failure 2. Instable Angina pectoris 3. Smokers 4. Ventricular tachyarrhythmias or AV-Block \>I° 5. Renal failure (\>200 umol) 6. Liver disease (ALT or AST \>150 IU) 7. Diabetes mellitus 8. Obesity (BMI \>30 kg/m2) 9. Symptomatic hypotension, hypertension \>160/100mmHg 10. Known allergy to compounds of Nestlé noir intense 11. History of gastric ulcer or bleeding, current diarrhea 12. Venous thrombosis or pulmonary embolism, at present or recurrent history of Infectious disease, acutely or chronic 13. Disease with systemic inflammation (e.g. rheumatoid arthritis, M. Crohn) 14. Neoplasia (unless healed or remission \>5 years) 15. Participation in another study within the last month 16. Concomitant vitamin supplements

Design outcomes

Primary

MeasureTime frame
endothelial functionacute (2 hours), chronic (2 and 4 weeks)

Secondary

MeasureTime frame
shear-stress dependent platelet function; Oxidative stress; baroreceptor function Systemic inflammatory response (assessed as change in high sensitivity CRP, 8-Isoprostanes, CD-40 ligand); Plasma epicatechins.acute (2 hours), chronic (2 and 4 weeks)

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026