Registry evidence

Macular Degeneration & Vision and Platelet-rich plasma (PRP): what the trial registry contains

The ClinicalTrials.gov registry holds 5 records for PRP in Macular Degeneration & Vision: 1 recruiting now, 1 labelled Phase 3 or 4, across 3 countries. Snapshot 2026-08-29.

Medical review statusMedically reviewedReviewed by: Stem Plus medical teamReviewed on: 2026-08-29Last evidence update: 2026-08-29Methodology and editorial standards
Clinical review team: Dr Kamelia Milcheva, Hematologist · Dr Vadym Uvarov, Board-Certified Physician · Hepatobiliary Surgeon · Candidate of Medical SciencesEditorial responsibility: StemCellAtlas research teamEducational information only. This page does not provide medical advice, diagnosis or a treatment recommendation.

Why this is studied in Macular Degeneration & Vision

Age-related macular degeneration destroys retinal pigment epithelium and photoreceptors. Replacement of RPE from pluripotent sources is one of the most technically advanced cell programmes anywhere, with surgical delivery and detailed imaging endpoints. It is also an area where unregulated intravitreal injections have caused documented severe vision loss.

What PRP means in this table

Platelet-rich plasma is a blood product, not a stem-cell product, though it is routinely sold as part of the same package. Preparation varies enormously between systems — platelet concentration, leukocyte content and activation all differ — so the label describes a category of procedure rather than a defined substance, which is the main reason its trial literature is so inconsistent.

The numbers

Every figure below comes from one reproducible query (macular degeneration x platelet-rich plasma) run against ClinicalTrials.gov API v2 on 2026-08-29.

MetricValue
Registered studies (all statuses)5
Interventional studies in the sample5
Recruiting right now1
Completed3
Terminated, withdrawn or suspended0
Phase 3 or Phase 4 records1
Countries with at least one site3
Median planned enrolment28 participants
Largest single planned enrolment36 participants
First / most recent start year2018 — 2025

How mature is this evidence?

Later-phase work exists but is not dominant (1 of 5), which is the typical profile of a field that has shown safety and is still testing whether benefit survives a control arm.

0 of these records (0%) were terminated, withdrawn or suspended, against 3 marked completed; unfinished studies rarely appear in marketing summaries.

Phase labelRecordsShare
Not applicable350%
Phase 1117%
Phase 2117%
Phase 3117%

Median planned enrolment is 28 participants (largest single study: 36). Trials of this size can describe safety and generate hypotheses; detecting a modest clinical benefit reliably usually needs substantially larger numbers with a control group.

Where the studies are

Country coverage runs to 3, but the distribution has a long tail behind Italy at about 40% of mentions.

CountryStudies with a site there
Italy2
Turkey (Türkiye)2
Brazil1

Legal pathway differs by country — see where cell therapy is legal, by country.

Who runs them

Lead sponsors split roughly 4 academic or hospital against 1 commercial — a academic profile. Commercial sponsorship is not a red flag by itself, but it changes publication incentives.

  • Fondazione Policlinico Universitario Agostino Gemelli IRCCS — 2 records
  • Rubens Camargo Siqueira — 1 record
  • Ankara Universitesi Teknokent — 1 record
  • Marmara University Pendik Training and Research Hospital — 1 record

Representative registered studies

Recruiting studies first, then the most advanced phases. Each identifier links to the registry record, where eligibility criteria, outcome measures and contacts are published.

StudyPhaseStatusPlanned nLead sponsorStart
NCT05706896 — Atrophic Age-related Macular Degeneration Treated With Intravitreal Injections of Umbilical Cord Blood Platelet-rich Plasman/aRecruiting36Fondazione Policlinico Universitario Agostino Gemelli IRCCS2022-12-14
NCT07341919 — Subtenon Autologous Platelet-Rich Plasma in Inherited and Degenerative Retinal DiseasesPhase 1, Phase 2Active Not Recruiting30Rubens Camargo Siqueira2025-01-04
NCT04636853 — CB-PRP in Retinitis Pigmentosa and Dry Age-related Macular DegenerationPhase 3Completed20Fondazione Policlinico Universitario Agostino Gemelli IRCCS2020-12-23
NCT07428798 — Subtenon PRP Injection for Geographic Atrophy in Dry Age-Related Macular Degenerationn/aCompleted14Marmara University Pendik Training and Research Hospital2024-07-01
NCT04242719 — Management of Deep Retinal Capillary Ischemia by Electromagnetic Stimulation and Platelet- Rich Plasman/aCompleted28Ankara Universitesi Teknokent2018-01-01

What this page does and does not tell you

None of these numbers say the therapy works. They say how much organised research exists and how far along it is; effect sizes live in published results, not registry entries.

If a clinic offers you this today, the useful question is not "is there research?" but "which of these registered studies is mine part of, and if none, what evidence applies to the exact product I am being sold?" The Provider Question Builder turns that into a scored checklist.

Frequently asked

How many PRP studies for Macular Degeneration & Vision are recruiting right now?

1 of 5 registered records were listed as recruiting in the 2026-08-29 snapshot. Recruitment status changes frequently; the registry record is authoritative.

Is PRP an approved treatment for Macular Degeneration & Vision?

Registration on ClinicalTrials.gov is not approval. Approval is granted by a regulator for a specific product and indication after review of submitted evidence. 5 registered studies tell you research exists, not that a product cleared review.

How advanced is the research on PRP for Macular Degeneration & Vision?

1 of 5 records carry a Phase 3 or Phase 4 label and 3 are marked completed. Registrations run from 2018 to 2025.

Registry and literature counts retrieved 2026-08-29 (ClinicalTrials.gov API v2; PubMed E-utilities). Registration or publication volume measures research activity, not effectiveness or approval. Educational information — not medical advice; verify product, indication, legal pathway and evidence with an independent qualified physician. Page generated 2026-08-29. See our editorial standards.

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Query totals are full API matches; status, phase and country counts describe the first up to 400 returned records per query. Query classes overlap and must not be summed as unique trials. Counts are not treatment outcomes. Snapshot: 2026-08-29. Methods and field definitions.