Skip to content

The effect of lipoic acid supplementation on stroke patients

The effect of alpha-lipoic acid supplementation on some cardiovascular indicators, inflammatory markers, and lipid profile in patients with stroke

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016051811763N23
Enrollment
80
Registered
2016-06-29
Start date
2016-05-21
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

strok. Stroke, not specified as haemorrhage or infarction

Interventions

Intervention 1: lipoic acid 600 mg. Intervention 2: corn starch 600 mg.
Treatment - Drugs
Placebo
lipoic acid 600 mg
corn starch 600 mg

Sponsors

Vice President of Research, Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
30 Years to 70 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with thrombotic and embolic stroke ; NIHS Score = 5-24 ; age 30 to 70 years; BMI in the range of 18.5-35. exclusion criteria: unwillingness to continue; recurrent stroke during the study; death.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Carotid intima media thickness. Timepoint: Before and 12 weeks after intervention. Method of measurement: sonography doppler.;Flow mediated dilation. Timepoint: Before and 12 weeks after intervention. Method of measurement: sonography doppler.;TNF-a. Timepoint: Before and 12 weeks after intervention. Method of measurement: ELISA.;IL-6. Timepoint: Before and 12 weeks after intervention. Method of measurement: ELISA.;Hs-CRP. Timepoint: Before and 12 weeks after intervention. Method of measurement: ELISA.;TG. Timepoint: Before and 12 weeks after intervention. Method of measurement: kit.;Total cholesterol. Timepoint: Before and 12 weeks after intervention. Method of measurement: Enzymatic.;LDL. Timepoint: Before and 12 weeksafter intervention. Method of measurement: Friedewald.;HDL. Timepoint: Before and 12 weeks after intervention. Method of measurement: Spectrophotometry.;Fasting blood glucose. Timepoint: Before and 12 weeks after intervention. Method of measurement: Spectrophotometry.;Fasting insulin. Timepoint: Before and 12 weeks after intervention. Method of measurement: ELISA.;Systolic blood pressur. Timepoint: Before and 12 weeks after intervention. Method of measurement: Mercury manometers.;Diastolic blood pressur. Timepoint: Before and 12 weeks after intervention. Method of measurement: Mercury manometer.

Secondary

MeasureTime frame
Carotenoids intake. Timepoint: before and 12 weeks after intervention. Method of measurement: 24 food recall.;Weight. Timepoint: before and 12 weeks after intervention. Method of measurement: seca balance.;Waist circumference. Timepoint: before and 12 weeks after intervention. Method of measurement: tape.;Energy intake. Timepoint: before and 12 weeks after intervention. Method of measurement: 24 food recall.;Carbohydrate intake. Timepoint: before and 12 weeks after intervention. Method of measurement: 24 food recall.;Fat intake. Timepoint: before and 12 weeks after intervention. Method of measurement: 24 food recall.;Protein intake. Timepoint: before and 12 weeks after intervention. Method of measurement: 24 food recall.;Vitamin E intake. Timepoint: before and 12 weeks after intervention. Method of measurement: 24 food recall.;Vitamin C intake. Timepoint: before and 12 weeks after intervention. Method of measurement: 24 food recall.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactVida Mohammadi

Isfahan University of Medical Sciences

Mohammadi_vida@yahoo.com+98 31 3792 3171

Outcome results

None listed

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