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Effect of combined selenium and Coenzyme Q10 on heart failure treatment

Effect of combined selenium and Coenzyme Q10 on left ventricular function and functional capacity in patients with heart failure (left ventricular dysfunction)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2013020512371N1
Enrollment
64
Registered
2013-10-28
Start date
2013-10-07
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

Condition 1: Heart failure. Condition 2: Heart failure. Congestive heart failure Left ventricular failure

Interventions

Intervention 1: intervention group: co Q10 30 mg TID selenium 200 mcg OD. Intervention 2: control group: 2kind of Placebo as form of co q10 and selenium.
Treatment - Drugs
intervention group: co Q10 30 mg TID selenium 200 mcg OD
control group: 2kind of Placebo as form of co q10 and selenium

Sponsors

Medical Research Department of Isfahan University
Lead Sponsor
Exir Pharmaceutical Companies
Collaborator

Eligibility

Sex/Gender
All
Age
35 Years to 85 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Male and female with ischemic and nonischemic heart failure; aged between 30 to 85 years old; LVEF less than 50% (with simpson method);NYHA CLASS 2,3; stability for 1month with no change in dose and kind of drugs in at least one month perior. Exclusion criteria: ACS or Revascularization procedure in 1month before or during study;heart failure with killip class 3, 4; active Myocarditis and pricarditis; uncontroled HTN; severe renal dysfunction (GFR less than 30%); pulmonary dysfunction( PCO2 more than 45 and Po2 less than 60); liver dysfunction(CHILD 2,3).

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
EF (Simpson). Timepoint: before intervention- after 3 month inetrvention. Method of measurement: echocardiography.;Functional calss with NYHAN CLASS. Timepoint: BEFORE INTERVENTION-3MONTH LATER. Method of measurement: questionair.

Secondary

MeasureTime frame
Gastrointestinal symptoms/diarrhea. Timepoint: at the end of each mounth. Method of measurement: interview.;Echocardiography parameter (LVEF Mmode, EDD, ESD). Timepoint: after and before intervention. Method of measurement: echocardiography.;Skin rash. Timepoint: each month. Method of measurement: inteview.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Parvin Bahrami

Isfahan University of Medical Sciences

p_bahrami.2010@yahoo.com+98 31 1212 3413

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026