HCFMUSP
São Paulo, 05410020, Brazil
Location contact
Giancarlo Fatobene, MD, PhD
PRINCIPAL_INVESTIGATOR
Victoria Sousa
CONTACT
NCT Number: NCT07014059
Autologous serum eye drops (ASED) are an established therapy for ocular surface diseases; however, their preparation can be costly and may not be available due to the need for germ-free conditions. This pilot trial assesses the feasibility of collecting ASED in a closed-circuit system for patients with chronic ocular surface diseases.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Phase 2
São Paulo, 05410020, Brazil
Giancarlo Fatobene, MD, PhD
PRINCIPAL_INVESTIGATOR
Victoria Sousa
CONTACT
Autologous Serum exhibits characteristics very similar to those of tears, such as pH, osmolarity, vitamins, and Immunoglobulin A. It also contains growth factors, nutritional factors, and antibacterial components that are necessary for the maintenance of cellular viability in the epithelial repair process. The use of autologous serum eye drops was first described in 1984 by Fox et al., in research for a preservative-free tear substitute. Subsequently, in 1999, Tsubota et al. found that, due to the presence of growth factors and vitamins, autologous serum could have a true epithelial trophic potential for the ocular surface. The autologous serum eye drops are not only a lubricant for the ocular surface but also provide various essential substances for the reconstruction of epithelial damage, including vitamin A, epithelial growth factor, fibronectin, and a variety of cytokines. With these epithelial trophic factors, autologous serum facilitates proliferation, migration, and differentiation of the ocular surface epithelium. Moreover, it is known for its anti-catabolic properties, inhibiting the inflammatory cascade triggered by interleukin-1, which prevents tissue destruction. Therefore, autologous serum eye drops have been effective in the treatment of persistent epithelial defects, neurotrophic ulcers, superior limbic keratoconjunctivitis, dry eye conditions, graft-versus-host disease (GVHD), or after refractive surgeries, such as LASIK (Laser Assisted In Situ Keratomileusis). In 2020, Wang et al. published an article with 7 randomized controlled trials comparing the use of autologous serum versus artificial tears in patients with dry eye syndrome. In the meta-analysis, all 7 studies evaluated subjective symptoms and showed that autologous serum eye drops were superior to ocular lubricants in alleviating and remitting symptoms. It was shown that autologous serum eye drops significantly improved parameters such as OSDI (Ocular Surface Disease Index), tear break-up time, and Bengal Rose staining when compared to the control group using ocular lubricants. Given the numerous properties of autologous serum eye drops, there is no doubt about their benefit and effectiveness in treating several ocular surface diseases, including ocular GVHD. However, the difficulty in accessing production and the substantial cost of autologous serum eye drops are the main challenges, and their use is often limited to more severe dry eye cases and those refractory to conventional treatment.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The collection of autologous serum in a closed blood processing system for ocular use
Time frame: 2 years
Proportion of blood collections that resulted in successful production of final autologous serum containers suitable for patient use.
Time frame: 2 years
0.0-0.03x10ˆ3/mcL;
Time frame: 2 years
0.0-0.03x10ˆ6/mcL;
Time frame: 2 years
0.0-0.03x10ˆ3/mcL;
Time frame: 2 years
7.00-7.50;
Time frame: 2 years
Positive or negative;
Time frame: baseline, 6 weeks, 12 weeks, and end of treatment
0-3
Time frame: Baseline, 6 weeks, 12 weeks, and end of treatment
Reported by the patient from 0 to 100
Time frame: Baseline, 6 weeks, 12 weeks, and end of treatment
Reported by the patient from 0 to 10
Time frame: Baseline, 6 weeks, 12 weeks, and end of treatment
Reported by the patient from 0 to 100
Time frame: Baseline, 6 weeks, 12 weeks
Bijsterveld scale: 0-9.
Time frame: Baseline, 6 weeks, 12 weeks
Bijsterveld scale: 0-9.
Time frame: Baseline, 6 weeks, 12 weeks
Good, moderate, poor
Time frame: Baseline, 6 weeks, 12 weeks
0-30 mm in 5 minutes
Time frame: Baseline, 6 weeks, 12 weeks
0-50 seconds
Time frame: Baseline, 6 weeks, 12 weeks
0-3
Time frame: At 6 and 12 weeks post-treatment
Percentage of doses administered vs. planned doses: 0-100%
Time frame: At 12 weeks post-treatment
Qualitative questionnaire
Time frame: At 50% of planned recruitment
Qualitative questionnaire
Time frame: two years
EGF, PDGF, NGF, Substance P, hialuronic acida, vitamin A and Vitamin D
Contact information is provided by the study sponsor or research team.
GIANCARLO FATOBENE
Other
"In Vivo Evaluation of Topical Ocular Use of Autologous Serum Obtained by a Closed-Circuit Collection Device."
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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