Condition (MeSH)
Hand Deformities, Congenital
ClinicalTrials.gov lists 4 trials for Hand Deformities, Congenital or a narrower condition beneath it.
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Trials per phase
4 of the 4 trials are tagged with Hand Deformities, Congenital itself; the rest are tagged with a narrower condition beneath it.
When did Hand Deformities, Congenital trials start? (4)
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 over time, by phase
- Phase 4
- Observational
Top of scale: 1
Trials registered with a start date in each year, 1990 onward, stacked by phase (complete years only; the current partial year is in the table's notes). The table below lists the same counts, most recent years first.
| Year | Trials started |
|---|---|
| 2026 (partial year) | 1 |
| 2023 | 1 |
| 2021 | 1 |
| 2004 | 1 |
No forecast is made for this condition: it averages 0.4 trial starts a year over the five years to September, under the 5 a year the method needs.
Recruitment duration, a model prediction: 1 trial still running at the 2026-10-09 snapshot, fewer than the 5 needed for a median. Source: ClinicalTrials.gov / AACT (CTTI), public domain.
What phase are Hand Deformities, Congenital trials in? (3)
Shown in this order: phase order.
Show the trials by phase as a table
| Phase | Trials |
|---|---|
| Phase 4 | 1 |
| Not applicable | 1 |
| Observational | 2 |
How many Hand Deformities, Congenital trials are recruiting? (3)
Shown in this order: the order a trial moves through, from not yet recruiting to unknown.
| Status | Trials |
|---|---|
| Recruiting | 1 |
| Completed | 2 |
| Unknown status | 1 |
Status as registered on ClinicalTrials.gov. Each trial is counted once.
Which publications cover Hand Deformities, Congenital? (22)
Shown in this order: major-topic papers first, then newest, then most linked to trials.
| Publication | Journal | Year | Major topic |
|---|---|---|---|
| Thirteen Indians with camptodactyly-arthropathy-coxa vara-pericarditis syndrome. | Clinical dysmorphology | 2024 | Yes |
| Oculoplastic surgery, diagnosis, and other matters in Freeman-Burian syndrome. | Ophthalmic genetics | 2022 | Yes |
| Findings, Phenotypes, Diagnostic Accuracy, and Treatment in Freeman-Burian Syndrome. | The Journal of craniofacial surgery | 2020 | Yes |
| Genotype-phenotype investigation of 35 patients from 11 unrelated families with camptodactyly-arthropathy-coxa vara-pericarditis (CACP) syndrome. | Molecular genetics & genomic medicine | 2018 | Yes |
| CACP syndrome: identification of five novel mutations and of the first case of UPD in the largest European cohort. | European journal of human genetics : EJHG | 2014 | Yes |
Showing 5 of 22 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.