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Condition (MeSH)

Elliptocytosis, Hereditary

ClinicalTrials.gov lists 2 trials for Elliptocytosis, Hereditary or a narrower condition beneath it.

MeSH D004612 Hemic and Lymphatic Diseases C15 C16 Listed by Orphanet as a rare disease
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Trials started per year Trials started per year 2 Trials by phase Trials by phase 1 Trials by recruitment status Trials by recruitment status 1 Publications Publications 2 Prevalence Prevalence 3 Rare-disease identity Rare-disease identity 2 Trials started per year Trials started per year 2 Trials by phase Trials by phase 1 Trials by recruitment status Trials by recruitment status 1 Publications Publications 2 Prevalence Prevalence 3 Rare-disease identity Rare-disease identity 2

Rows recorded per section

3 sections measured, none recorded · 1 not measured yet · 1 not computed

2 of the 2 trials are tagged with Elliptocytosis, Hereditary itself; the rest are tagged with a narrower condition beneath it.

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The PDF carries up to 50 rows of each section, where the page shows the first few, with the sources listed. Enter a work email and confirm it from the message we send, and the report follows by email.

When did Elliptocytosis, Hereditary 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
2020 1
2008 1

No forecast is made for this condition: it averages 0.0 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 Elliptocytosis, Hereditary trials in? (1)

Shown in this order: phase order.

Trials by phase
Phase Trials
Observational 2

How many Elliptocytosis, Hereditary trials are recruiting? (1)

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

Trials by recruitment status
Status Trials
Completed 2

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

Which publications cover Elliptocytosis, Hereditary? (2)

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

Publications
Publication Journal Year Major topic
Placental malaria in women with South-East Asian ovalocytosis. The American journal of tropical medicine and hygiene 2006 Yes
Disorders of red cell membrane. British journal of haematology 2008 No

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
Hereditary elliptocytosis Point prevalence 1-5 / 10 000 Worldwide Not stated Exact
Hereditary elliptocytosis Point prevalence 1-5 / 10 000 Worldwide Not stated Unspecified
Hereditary elliptocytosis Point prevalence 1-5 / 10 000 Worldwide Not stated Exact

Rare-disease identity (2)

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

Rare-disease identity
Orphanet disease ORPHA code Relation Source
Hereditary elliptocytosis 288 Exact Orphanet Rare Disease Ontology (ORDO)
Hereditary elliptocytosis 288 Exact Orphadata Science knowledge files, Product 1

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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