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The study of coenzyme Q10 supplementation on blood pressure, inflammation factors& Adiponectin in hypertensive patients

The study of coenzyme Q10 supplementation on blood pressure, inflammation factors& Adiponectin in hypertensive patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201103086002N1
Enrollment
72
Registered
2011-05-29
Start date
2011-03-11
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

hypertension. High blood pressure

Interventions

Intervention 1: Placebo, 100 mg, once daily for three months. Intervention 2: Coenzyme q10, 100 mg orally, once daily for three months.
Placebo
Treatment - Drugs
Placebo, 100 mg, once daily for three months
Coenzyme q10, 100 mg orally, once daily for three months

Sponsors

Shahid Sadughi University of Medical Sciences and Health Services
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to 55 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: willingness to cooperate in the project and complete a written informed consent, diagnosis of hypertensive patients based on diagnostic criteria and clinical examination by a physician, No pregnant or breastfeeding women, the absence of any autoimmune disorders, cardio - vascular, or renal diseases, lack of nutritional supplements during the past six months Exclusion criteria: diabetes mellitus type 1 or type 2, the history of disease such as myocardial infarction, cardiac dysfunction, cardiac arrhythmia, angina and kidney disease, autoimmune diseases like MS, rheumatism, etc, BMI> 40, factors causing secondary hypertension, supplementation of vitamin, mineral or other nutritional supplements, Alcohol or drug use, Incidence of severe side effects, non-compliance with study protocol

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
IL6. Timepoint: At baseline, after the sixth week and twelfth week baseline. Method of measurement: ELISA.;Hypertension. Timepoint: At At baseline, weeks after the sixth and twelfth week baseline. Method of measurement: Measured by standard mercury blood pressure measuring device sitting.;IL2. Timepoint: At baseline, after the sixth week and twelfth week baseline. Method of measurement: ELISA.;Hs-CRP. Timepoint: At baseline, after the sixth week and twelfth week baseline. Method of measurement: ELISA.;TNF-a. Timepoint: At baseline, after the sixth week and twelfth week baseline. Method of measurement: ELISA.;Adiponectin. Timepoint: At baseline, after the sixth week and twelfth week baseline. Method of measurement: ELISA.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSeied Mohammad Mohammadi Zarchi

Shahid Sadughi University of Medical Sciences and Health Services

drc@ssu.ac.ir+98 912 346 8307

Outcome results

None listed

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