Condition (MeSH)
XYY Karyotype
ClinicalTrials.gov lists 1 trial for XYY Karyotype or a narrower condition beneath it.
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Rows recorded per section
5 sections measured, none recorded · 1 not measured yet · 1 not computed
1 of the 1 trial is tagged with XYY Karyotype itself; the rest are tagged with a narrower condition beneath it.
When did XYY Karyotype 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 |
|---|---|
| 2024 | 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 1 trial evaluated at the 2026-10-09 snapshot is predicted and still running. Source: ClinicalTrials.gov / AACT (CTTI), public domain.
What phase are XYY Karyotype trials in? (1)
Shown in this order: phase order.
| Phase | Trials |
|---|---|
| Observational | 1 |
How many XYY Karyotype trials are recruiting? (1)
Shown in this order: the order a trial moves through, from not yet recruiting to unknown.
| Status | Trials |
|---|---|
| Enrolling by invitation | 1 |
Status as registered on ClinicalTrials.gov. Each trial is counted once.
Which publications cover XYY Karyotype? (6)
Shown in this order: major-topic papers first, then newest, then most linked to trials.
| Publication | Journal | Year | Major topic |
|---|---|---|---|
| Deep phenotypic analysis of psychiatric features in genetically defined cohorts: application to XYY syndrome. | Journal of neurodevelopmental disorders | 2023 | Yes |
| Modeling familial predictors of proband outcomes in neurogenetic disorders: initial application in XYY syndrome. | Journal of neurodevelopmental disorders | 2021 | Yes |
| Characterization of autism spectrum disorder and neurodevelopmental profiles in youth with XYY syndrome. | Journal of neurodevelopmental disorders | 2018 | Yes |
| 47,XXY (Klinefelter syndrome) and 47,XYY: estimated rates of and indication for postnatal diagnosis with implications for prenatal counselling. | Prenatal diagnosis | 1997 | Yes |
| The epidemiology of sex chromosome abnormalities. | American journal of medical genetics. Part C, Seminars in medical genetics | 2020 | No |
Showing 5 of 6 publications.
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, prevalence, rare-disease identity, and sub-conditions in mesh.
Not computed for conditions with fewer than 10 trials: drugs tested.