Fish Oil (Omega 3 ) in Sjogren's Syndrome
- Conditions
- Sjogren's Syndrome
- Interventions
- Drug: Omega 3 fatty acidDrug: Placebo
- Registration Number
- NCT05005806
- Lead Sponsor
- Hawler Medical University
- Brief Summary
Sjögren's syndrome (pSS) is an autoimmune disorder affecting mainly the exocrine glands.this lead to dryness of the main mucosal surface ,such as the mouth ,eye,skin nose,pharynx,larynx and vagina . The history of the disease is characterized by a slowly progression of sicca symptoms and fatigue; however, a subset of patients would experience extra glandular activity. Lipid mediators derived from polyunsaturated fatty acids, related to inflammation and immune response regulation. In this sense, the polyunsaturated fatty acids omega-3 (ω-3 FA) have been associated with several illnesses such as cancer, cardiovascular disease and autoimmune diseases and their balance at the cellular membranes can result in an anti-inflammatory .
- Detailed Description
this is a randomized double -blind placebo -controlled clinical trial .the participants will be randomize into two groups .Group 1 receive dietary omega-3 supplementation (omega-3 group) whereas Group 2(placebo group) receive a placebo . The two types are similar to each other in the form of soft gel ,both are given two times daily for two months with follow-up of patients whom they full fill the inclusion criteria.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 100
- Age≥ 18 and ≤ 70 years old .
- Able to provide inform consent
- Patients diagnosed as syndrome according to 2016 ACR(American college of Rheumatology)/ EULAR(European league Against Rheumatism classification criteria for Sjögren's syndrome
- any preexisting ocular disease or on eye drops lubricants.
- patients on (Beta blockers, Diuretics , anticholinergic, α 1antagonist and α 2 agonist ,anticoagulant, antidepressant, antihistamine ,pilocarpine, cevimeline ) .
- past history of diabetes, psychiatric disorder.
- pregnancy, lactating mother
- malignancy
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Omega 3 soft gel Omega 3 fatty acid participants in this group (1)omega 3 fatty acid soft gel 1000 mg will be given to participants twice daily for two months. placebo Placebo placebo group ,placebo soft gel designed same as omega 3 contain Vitamin A 1000 mg twice daily for two months
- Primary Outcome Measures
Name Time Method Dry mouth symptoms up to two months measure dry mouth by inventory xerostomia score is included 11 questionnaire which score calculated by visual analogue scale from 1 to 5 ( never to very often ) have symptoms
Dry eye symptoms up to two months subjective symptoms of dry eye which involve 6 symptoms( burning sensation, itching, foreign body sensation , Dryness, mucous discharge, photophobia) when absent(0) , sometime present (1) , frequently present (2), always present (3) ( score 0-6 mild, 6-12 moderate, 12-18 sever by visual analogue scale
- Secondary Outcome Measures
Name Time Method sialometry test up to two months measuring of salivary flow ,unstimulated whole saliva is collect when mouth rinse with distill water then the patient tow his head and try not to move during the test, a plastic disposable pipette drew the accumulated saliva in the floor of the mouth,for a period of five minute,the volume will record ,flow express as ml/min.
schirmers tear test up to two months patient will sitt in examining chair ,the test strip is bend with round wick and at indentation ( approximately 90 degree ) then patient instruct to look up and draw eye gently downward ,then round bend end of sterile strip hook over eyelid border at junction of middle and outer one third of the lower eyelid margin.
Trial Locations
- Locations (1)
Reumatology out patient clinic,
🇮🇶Erbil, Iraq