Munkholm 1999.
Study characteristics | ||
Methods | RCT with parallel design | |
Participants | 22 adult participants with NYHA II or III heart failure 11 participants in the treatment group and 11 in the placebo group Adults (> 18 years) Before and after the treatment period, a right heart catheterisation was done |
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Interventions | Intervention: oral coenzyme Q10 100 mg twice daily for 12 weeks Control: placebo |
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Outcomes | Baseline and post‐therapeutic serum levels of coenzyme Q10 Left ventricular ejection fraction NYHA clinical status |
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Notes | This study is an invasive study investigating the treatment of congestive heart failure | |
Risk of bias | ||
Bias | Authors' judgement | Support for judgement |
Random sequence generation (selection bias) | Unclear risk | Randomised, no information about random sequence generation provided. |
Allocation concealment (selection bias) | Unclear risk | No information given |
Blinding of participants and personnel (performance bias) All outcomes | Low risk | Double‐blind |
Blinding of outcome assessment (detection bias) All outcomes | Unclear risk | No information given |
Incomplete outcome data (attrition bias) All outcomes | Low risk | All participants completed the study |
Selective reporting (reporting bias) | Unclear risk | No study protocol was available |
Other bias | Low risk | No other risk of bias was found |