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Condition (MeSH)

Persistent Hyperplastic Primary Vitreous

ClinicalTrials.gov lists 2 trials for Persistent Hyperplastic Primary Vitreous or a narrower condition beneath it.

MeSH D054514 Eye Diseases C11 C16 Listed by Orphanet as a rare disease
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Phase 4 Phase 4 1 Not applicable Not applicable 1 Phase 4 Phase 4 1 Not applicable Not applicable 1

Trials per phase

2 of the 2 trials are tagged with Persistent Hyperplastic Primary Vitreous itself; the rest are tagged with a narrower condition beneath it.

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When did Persistent Hyperplastic Primary Vitreous trials start? (2)

Shown in this order: most recent first, 1990 onwards. 2026 is partial: trials registered with a 2026 start date so far, not a full year.

Trials started per year
Year Trials started
2024 1
2017 1

No forecast is made for this condition: it averages 0.2 trial starts a year over the five years to September, under the 5 a year the method needs.

Recruitment duration, a model prediction: none of the 2 trials evaluated at the 2026-10-09 snapshot is predicted and still running. Source: ClinicalTrials.gov / AACT (CTTI), public domain.

What phase are Persistent Hyperplastic Primary Vitreous trials in? (2)

Shown in this order: phase order.

Show the trials by phase as a table
Trials by phase
Phase Trials
Phase 4 1
Not applicable 1

How many Persistent Hyperplastic Primary Vitreous trials are recruiting? (2)

Shown in this order: the order a trial moves through, from not yet recruiting to unknown.

Trials by recruitment status
Status Trials
Recruiting 1
Unknown status 1

Status as registered on ClinicalTrials.gov. Each trial is counted once.

Which publications cover Persistent Hyperplastic Primary Vitreous? (2)

Shown in this order: major-topic papers first, then newest, then most linked to trials.

Publications
Publication Journal Year Major topic
Visual and Anatomical Outcomes With Vitrectomy in Posterior or Combined Persistent Fetal Vasculature in an Asian Population. Ophthalmic surgery, lasers & imaging retina 2019 Yes
Infant Aphakia Treatment Study: effects of persistent fetal vasculature on outcome at 1 year of age. Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus 2011 Yes

Prevalence (3)

Shown in this order: jurisdiction, then disease name. Orphanet observation for the mapped ORPHA concept; the mapping relation column says whether that concept is exactly this condition or broader or narrower.

Prevalence
Orphanet disease Type Class Geography Jurisdiction Mapping relation
Persistent hyperplastic primary vitreous Point prevalence Unknown Worldwide Not stated Exact
Persistent hyperplastic primary vitreous Point prevalence Unknown Worldwide Not stated Exact
Persistent hyperplastic primary vitreous Point prevalence Unknown Worldwide Not stated Unspecified

Rare-disease identity (2)

Shown in this order: exact, broader, narrower, other.

Rare-disease identity
Orphanet disease ORPHA code Relation Source
Persistent hyperplastic primary vitreous 91495 Exact Orphadata Science knowledge files, Product 1
Persistent hyperplastic primary vitreous 91495 Exact Orphanet Rare Disease Ontology (ORDO)

Not on this page

Not measured: delivery record.

Checked, with nothing recorded for this condition: lead sponsors, serious adverse events in this condition's trials, and sub-conditions in mesh.

Not computed for conditions with fewer than 10 trials: drugs tested.

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