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NCT Number: NCT07014059

Autologous Serum Obtained by a Closed-Circuit Collection Device

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.

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Key information

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • ≥ 18 years
  • Dry eye and/or chronic epithelial defects of the ocular surface with indication for autologous serum according to the evaluation of ophthalmologists specialized in Cornea and Ocular Surface;
  • Peripheral venous access or PICC that allows the collection of whole blood.

Exclusion criteria

  • Active ocular infection;
  • Hemoglobin < 11 g/dL;
  • Angina, MI, or stroke in the last 30 days;
  • Significant pulmonary or cardiac disease that contraindicates autologous serum collection in the investigator's opinion;
  • Active ocular or systemic infection at the time of collection;
  • Inability to attend follow-up visits at 6 and 12 weeks;
  • Active hematological malignancy (except measurable residual disease) or solid malignancy (except non-melanoma skin cancer);
  • Positive for HIV, HCV, HBV, HTLV, Chagas disease, or syphilis;
  • Life expectancy < 6 months;
  • Not pregnant (as reported by the participant).

Treatment and study plan

Autologous Serum 20%

Drug

The collection of autologous serum in a closed blood processing system for ocular use

Primary outcomes

  1. Feasibility of using the collection device under testing

    Time frame: 2 years

    Proportion of blood collections that resulted in successful production of final autologous serum containers suitable for patient use.

Secondary outcomes

  1. Median pre-freezing number of leukocytes in autologous serum

    Time frame: 2 years

    0.0-0.03x10ˆ3/mcL;

  2. Median pre-freezing number of red blood cells in autologous serum

    Time frame: 2 years

    0.0-0.03x10ˆ6/mcL;

  3. Median pre-freezing number of platelets in autologous serum

    Time frame: 2 years

    0.0-0.03x10ˆ3/mcL;

  4. Median pre and post-freezing pH in autologous serum

    Time frame: 2 years

    7.00-7.50;

  5. Pre-freezing microbiological test of autologous serum

    Time frame: 2 years

    Positive or negative;

  6. NIH ocular score

    Time frame: baseline, 6 weeks, 12 weeks, and end of treatment

    0-3

  7. Ocular Surface Disease Index

    Time frame: Baseline, 6 weeks, 12 weeks, and end of treatment

    Reported by the patient from 0 to 100

  8. Global ocular symptom score

    Time frame: Baseline, 6 weeks, 12 weeks, and end of treatment

    Reported by the patient from 0 to 10

  9. Lee score ocular subscale

    Time frame: Baseline, 6 weeks, 12 weeks, and end of treatment

    Reported by the patient from 0 to 100

  10. Corneal staining score (fluorescein)

    Time frame: Baseline, 6 weeks, 12 weeks

    Bijsterveld scale: 0-9.

  11. Corneal staining score (Rose Bengal)

    Time frame: Baseline, 6 weeks, 12 weeks

    Bijsterveld scale: 0-9.

  12. Meibography

    Time frame: Baseline, 6 weeks, 12 weeks

    Good, moderate, poor

  13. Schirmer test

    Time frame: Baseline, 6 weeks, 12 weeks

    0-30 mm in 5 minutes

  14. Non-invasive tear film break-up

    Time frame: Baseline, 6 weeks, 12 weeks

    0-50 seconds

  15. Tear film lipid layer

    Time frame: Baseline, 6 weeks, 12 weeks

    0-3

  16. Adherence to the use of autologous serum

    Time frame: At 6 and 12 weeks post-treatment

    Percentage of doses administered vs. planned doses: 0-100%

  17. Patient's qualitative evaluation of the use of autologous serum

    Time frame: At 12 weeks post-treatment

    Qualitative questionnaire

  18. Team's qualitative perception of the feasibility of collection and production of autologous serum

    Time frame: At 50% of planned recruitment

    Qualitative questionnaire

Other outcomes

  1. Pre- and post-growth factor in autologous serum

    Time frame: two years

    EGF, PDGF, NGF, Substance P, hialuronic acida, vitamin A and Vitamin D

Study contacts

Contact information is provided by the study sponsor or research team.

Giancarlo Fatobene, MD, PhD

CONTACT

[email protected]

+55 (11) 2661-9559 ext. 9559

Sponsors and collaborators

Lead sponsor

GIANCARLO FATOBENE

Other

Collaborators

  • JP Farma

Registry information

Official study title

"In Vivo Evaluation of Topical Ocular Use of Autologous Serum Obtained by a Closed-Circuit Collection Device."

Important dates

Study start
2025
Primary completion
2026
Study completion
2027
First posted
Jun 10, 2025
Registry last updated
Jun 10, 2025

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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