Condition (MeSH)
Duane Retraction Syndrome
ClinicalTrials.gov lists 1 trial for Duane Retraction Syndrome or a narrower condition beneath it.
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Rows recorded per section
3 sections measured, none recorded · 1 not measured yet · 1 not computed
1 of the 1 trial is tagged with Duane Retraction Syndrome itself; the rest are tagged with a narrower condition beneath it.
When did Duane Retraction Syndrome trials start? (1)
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.
| Year | Trials started |
|---|---|
| 2004 | 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 1 trial evaluated at the 2026-10-09 snapshot is predicted and still running. Source: ClinicalTrials.gov / AACT (CTTI), public domain.
What phase are Duane Retraction Syndrome trials in? (1)
Shown in this order: phase order.
| Phase | Trials |
|---|---|
| Observational | 1 |
How many Duane Retraction Syndrome trials are recruiting? (1)
Shown in this order: the order a trial moves through, from not yet recruiting to unknown.
| Status | Trials |
|---|---|
| Recruiting | 1 |
Status as registered on ClinicalTrials.gov. Each trial is counted once.
Which publications cover Duane Retraction Syndrome? (5)
Shown in this order: major-topic papers first, then newest, then most linked to trials.
| Publication | Journal | Year | Major topic |
|---|---|---|---|
| Loss of MAFB Function in Humans and Mice Causes Duane Syndrome, Aberrant Extraocular Muscle Innervation, and Inner-Ear Defects. | American journal of human genetics | 2016 | Yes |
| Understanding the Relationship Between Teacher Behavior and Motivation in Students with Acquired Deafblindness. | American annals of the deaf | 2016 | Yes |
| The genetic basis of incomitant strabismus: consolidation of the current knowledge of the genetic foundations of disease. | Seminars in ophthalmology | 2013 | Yes |
| CHN1 mutations are not a common cause of sporadic Duane's retraction syndrome. | American journal of medical genetics. Part A | 2010 | Yes |
| Expanding the Phenotype of the <i>FAM149B1</i>-Related Ciliopathy and Identification of Three Neurogenetic Disorders in a Single Family. | Genes | 2021 | 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.
| Orphanet disease | Type | Class | Geography | Jurisdiction | Mapping relation |
|---|---|---|---|---|---|
| Duane retraction syndrome | Point prevalence | 1-5 / 10 000 | Europe | Not stated | Exact |
| Duane retraction syndrome | Point prevalence | 1-5 / 10 000 | Europe | Not stated | Exact |
| Duane retraction syndrome | Point prevalence | 1-5 / 10 000 | Europe | Not stated | Unspecified |
Rare-disease identity (2)
Shown in this order: exact, broader, narrower, other.
| Orphanet disease | ORPHA code | Relation | Source |
|---|---|---|---|
| Duane retraction syndrome | 233 | Exact | Orphadata Science knowledge files, Product 1 |
| Duane retraction syndrome | 233 | 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.