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NCT05944757: prp

Compare of PRP Autologous Serum and Autologous Serum by Intrastromal Injection in Different Eye Disease Conditions

Status unknown NA Last updated 13 July 2023
What this trial tests

NA trial testing PRP plasma rich platelets in PRP in 40 participants. Status unknown.

Timeline
1 September 2021
Primary endpoint
1 September 2023
1 September 2024

Quick facts

Lead sponsorAnita Syla Lokaj
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment40
Start date1 September 2021
Primary completion1 September 2023
Estimated completion1 September 2024
Sites1 location across Kosovo

Drugs / interventions tested

Conditions studied

Sponsor

Anita Syla Lokaj — full company profile →

Who can join

Adults 20 to 70, any sex, with PRP. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Platelet-rich plasma (PRP) is an autologous blood product rich in proteins and growth factors. Its application has been the subject of many studies in the field of ophthalmology to stimulate tissue healing and regeneration. Due to its anatomical features (lack of blood vessels), the cornea is among the most susceptible to damage structures of the eye. Therefore, the study of the impact of various regenerative therapies (autologous blood products, serums, ) on corneal lesions is important not only scientifically, but also practically for ophthalmologist. Numerous reports described the healing effect of PRP on corneal lesions.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of PRP plasma rich platelets

Trials testing the same drug.

Other recruiting trials for PRP

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05944757.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing