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Fish oil supplementation for mild to moderate rosacea: a randomized, double-blind, cross-over controlled clinical study

Fish oil supplementation for mild to moderate rosacea: a randomized, double-blind, cross-over controlled clinical study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400088891
Enrollment
Unknown
Registered
2024-08-28
Start date
2024-09-01
Completion date
Unknown
Last updated
2024-09-02

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

Conditions

rosacea

Interventions

A:Phase 1 (0-8 weeks) : fish oil treatmentl Phase 2 after enrollment (weeks 8-16) : placebo
B:Phase 1 after enrollment (weeks 0-8) : Placebo Phase 2 (8-16 weeks) : fish oil treatment

Sponsors

Shanghai Skin Disease Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: ? 18-65 years old, male or female; ? patients with mild-to-moderate erythema telangiectasia rosacea diagnosed by a dermatologist (CEA score 1-3); ? patients with mild papulopustular rosacea diagnosed by dermatologists (IGA score 1-2); ? sign informed consent form voluntarily

Exclusion criteria

Exclusion criteria: ? women who are pregnant and lactating or who are planning a recent pregnancy ? patients with diabetes mellitus, moderate to severe liver, kidney, lung, blood and other systemic diseases, mental disorders ? Rosacea patients with nasal hypertrophy ? digestive and absorption dysfunction (achorhydria, acute or chronic gastrointestinal ulcer or duodenal surgery) 5) Allergies to seafood ? Long-term self-supplementation of fish oil (can be included after a washout period of more than 8w) ? Oral monoamine oxidase inhibitors (such as phenelzine, seligiline) ? Facial manifestations associated with other facial skin diseases, such as dermatomyositis or systemic lupus erythematosus ? Patients who are not expected to adhere to follow-up ? who participated in any clinical trial within one month ?Other circumstances considered by the investigator to be ineligible for inclusion

Design outcomes

Primary

MeasureTime frame
CEA score;

Secondary

MeasureTime frame
IGA score;Rosacea Patient Quality of Life Scale;Anxiety and depression rating scale;Dermoscopy;Transconfocal microscopy (RCM) was used for examination;Facial VISIA;Assessment of skin barrier function;

Countries

China

Contacts

Public ContactPeiru Wang

Shanghai Skin Disease Hospital

wpeiru@qq.com+86 138 1820 3016

Outcome results

None listed

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