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Condition (MeSH)

Amelogenesis Imperfecta

ClinicalTrials.gov lists 8 trials for Amelogenesis Imperfecta or a narrower condition beneath it.

MeSH D000567 Stomatognathic Diseases C07 C16 Listed by Orphanet as a rare disease
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Not applicable Not applicable 3 Observational Observational 5 Not applicable Not applicable 3 Observational Observational 5

Trials per phase

8 of the 8 trials are tagged with Amelogenesis Imperfecta itself; the rest are tagged with a narrower condition beneath it.

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When did Amelogenesis Imperfecta trials start? (7)

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

  • Not applicable
  • Observational

Top of scale: 2

2009: 1 trials (Observational 1) 2014: 1 trials (Not applicable 1) 2016: 1 trials (Not applicable 1) 2019: 1 trials (Not applicable 1) 2021: 1 trials (Observational 1) 2022: 2 trials (Observational 2) 2025: 1 trials (Observational 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.

Trials started per year
Year Trials started
2025 1
2022 2
2021 1
2019 1
2016 1
2014 1
2009 1

No forecast is made for this condition: it averages 0.6 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 8 trials evaluated at the 2026-10-09 snapshot is predicted and still running. Source: ClinicalTrials.gov / AACT (CTTI), public domain.

What phase are Amelogenesis Imperfecta trials in? (2)

Shown in this order: phase order.

Show the trials by phase as a table
Trials by phase
Phase Trials
Not applicable 3
Observational 5

How many Amelogenesis Imperfecta trials are recruiting? (4)

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

Trials by recruitment status
Status Trials
Recruiting 2
Completed 3
Terminated 1
Unknown status 2

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

Which publications cover Amelogenesis Imperfecta? (9)

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

Publications
Publication Journal Year Major topic
SLC13A5 is the second gene associated with Kohlschütter-Tönz syndrome. Journal of medical genetics 2017 Yes
Amelogenesis Imperfecta: 1 Family, 2 Phenotypes, and 2 Mutated Genes. Journal of dental research 2016 Yes
Developmental defects of enamel and dentine: challenges for basic science research and clinical management. Australian dental journal 2014 Yes
Protocol GenoDENT: Implementation of a New NGS Panel for Molecular Diagnosis of Genetic Disorders with Orodental Involvement. Methods in molecular biology (Clifton, N.J.) 2019 No
Molar incisor hypomineralisation (MIH) training manual for clinical field surveys and practice. European archives of paediatric dentistry : official journal of the European Academy of Paediatric Dentistry 2017 No

Prevalence (12)

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
Amelogenesis imperfecta Point prevalence 1-9 / 100 000 United States US Unspecified
Amelogenesis imperfecta Point prevalence 1-9 / 100 000 United States US Exact
Amelogenesis imperfecta Point prevalence 1-9 / 100 000 United States US Exact
Amelogenesis imperfecta Point prevalence >1 / 1000 Sweden Not stated Exact
Amelogenesis imperfecta Point prevalence Unknown 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
Amelogenesis imperfecta 88661 Exact Orphadata Science knowledge files, Product 1
Amelogenesis imperfecta 88661 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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