Comparison of the efficacy and safety of platelet-rich-plasma and autologous-serum eye drops in primary Sjögren syndrome dry eyes
Not Applicable
Completed
- Conditions
- Diseases of the musculoskeletal system and connective tissue
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 36
Inclusion Criteria
Moderate to severe dry eye who diagnosed as Sjogren syndrome
Exclusion Criteria
patients who had other systemic diseases, who had received other eye drops, systemic steroid or immunosuppressive treatment within the previous three months, who had undergone ocular surgery within the previous three months
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Corneal and conjunctival staining scores
- Secondary Outcome Measures
Name Time Method Corneal and conjunctival staining scores;Schirmer I value ;Tear break up time;Ocular Surface Disease Index;Conjunctival impression cytology metaplasia and goblet-cell density
Related Research Topics
Explore scientific publications, clinical data analysis, treatment approaches, and expert-compiled information related to the mechanisms and outcomes of this trial. Click any topic for comprehensive research insights.
What molecular mechanisms underlie PRP and autologous serum efficacy in Sjögren syndrome dry eye?
How does platelet-rich plasma compare to standard-of-care treatments for moderate to severe dry eye syndrome?
Which biomarkers correlate with treatment response in Sjögren syndrome patients using PRP or autologous serum eye drops?
What adverse events are associated with platelet-rich plasma therapy for dry eye disease and how are they managed?
Are there combination therapies involving PRP and other regenerative agents for Sjögren syndrome dry eye treatment?