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The role of omega 3 on the side effect of isotretinoin

Evaluation the role of omega 3 on the side effect of isotretinoin in the acnea vulgaris

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201306238241N2
Enrollment
118
Registered
2013-07-16
Start date
2013-06-15
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

Acnea vulgaris. Acne vulgaris

Interventions

Intervention 1: cap Omega 3 /BD/for 4 months+20 mg isotretinoin in interventional group. Intervention 2: cap isotretinoin 20 mg daily in control group.
Treatment - Drugs
cap Omega 3 /BD/for 4 months+20 mg isotretinoin in interventional group
cap isotretinoin 20 mg daily in control group

Sponsors

Vice chancellor for research and education
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 35 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: patients with moderate or severe acne (both sexes between the ages of 15 to 35 years old) who do not respond to conventional treatment. Exclusion criteria: patients with hyperlipidemia; hepatitis; lactating pregnant; women not wanting to have long contraception; omega 3 and vitamins A intake; allergy to seafood; aspirin or warfarin use and bleeding disorders .

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Side effect of isotretinoin. Timepoint: In weeks 4, 8, 12 and 16. Method of measurement: Check list.

Secondary

MeasureTime frame
Facial erythema. Timepoint: In weeks 4, 8, 12 and 16. Method of measurement: Check list.;Facial dryness. Timepoint: In weeks 4, 8, 12 and 16. Method of measurement: Check list.;Scaling of lip. Timepoint: In weeks 4, 8, 12 and 16. Method of measurement: Check list.;Body skin dryness. Timepoint: In weeks 4, 8, 12 and 16. Method of measurement: Check list.;Cheilitis. Timepoint: In weeks 4, 8, 12 and 16. Method of measurement: Check list.;Crust in nose. Timepoint: In weeks 4, 8, 12 and 16. Method of measurement: Check list.;Epistaxis. Timepoint: In weeks 4, 8, 12 and 16. Method of measurement: Check list.;Eye irritation. Timepoint: In weeks 4, 8, 12 and 16. Method of measurement: Check list.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mirnezami? Mina

Arak University of Medical Sciences

dr.mirnezami@arakmu.ac.ir+98 86 1224 1411

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 24, 2026