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Condition (MeSH)

Congenital Microtia

ClinicalTrials.gov lists 33 trials for Congenital Microtia or a narrower condition beneath it. Auregen Biotherapeutics, SA has the most among industry and government lead sponsors, with 3.

MeSH D065817 Otorhinolaryngologic Diseases C09 C16 Listed by Orphanet as a rare disease
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Phase 1 Phase 1 3 Phase 1/2 Phase 1/2 3 Phase 2 Phase 2 2 Phase 4 Phase 4 2 Not applicable Not applicable 15 Observational Observational 8 Phase 1 Phase 1 3 Phase 1/2 Phase 1/2 3 Phase 2 Phase 2 2 Phase 4 Phase 4 2 Not applicable Not applicable 15 Observational Observational 8

Trials per phase

33 of the 33 trials are tagged with Congenital Microtia itself; the rest are tagged with a narrower condition beneath it.

Get the Congenital Microtia report as a PDF

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 Congenital Microtia trials start? (12)

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 1
  • Phase 1/2
  • Phase 2
  • Phase 4
  • Not applicable
  • Observational

Top of scale: 5

2009: 1 trials (Phase 1 1) 2013: 1 trials (Observational 1) 2015: 1 trials (Phase 4 1) 2018: 1 trials (Observational 1) 2019: 1 trials (Not applicable 1) 2020: 4 trials (Not applicable 3, Phase 4 1) 2021: 3 trials (Observational 1, Not applicable 1, Phase 1/2 1) 2022: 5 trials (Observational 3, Not applicable 1, Phase 1 1) 2023: 5 trials (Observational 1, Not applicable 2, Phase 2 1, Phase 1 1) 2024: 4 trials (Not applicable 1, Phase 2 1, Phase 1/2 2) 2025: 3 trials (Not applicable 3)

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
2026 (partial year) 4
2025 3
2024 4
2023 5
2022 5
2021 3
2020 4
2019 1
2018 1
2015 1

No forecast is made for this condition: it averages 4.6 trial starts a year over the five years to September, under the 5 a year the method needs.

Prediction, not a registry value: median of 27 months from start to primary completion across 6 trials still running at the 2026-10-09 snapshot; registered median of 21 months across 14 trials with a primary completion typed Actual. Source: ClinicalTrials.gov / AACT (CTTI), public domain.

What phase are Congenital Microtia trials in? (6)

Shown in this order: phase order.

Show the trials by phase as a table
Trials by phase
Phase Trials
Phase 1 3
Phase 1/2 3
Phase 2 2
Phase 4 2
Not applicable 15
Observational 8

How many Congenital Microtia trials are recruiting? (7)

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

Trials by recruitment status
Status Trials
Not yet recruiting 3
Recruiting 4
Active, not recruiting 2
Completed 9
Terminated 5

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

Which lead sponsors run the most Congenital Microtia trials? (2)

Shown in this order: most trials first. Lead sponsors the registry classes as industry, NIH, US federal, other government or network. A hospital or university the registry files as government can appear here. Sponsors it classes as academic or other are shown on the full page, because that class cannot separate an institution from a named investigator.

Lead sponsors
Sponsor Trials
Auregen Biotherapeutics, SA 3
3DBio Therapeutics 1

Interventions as named in the registry (10)

Shown in this order: most trials first.

Interventions as named in the registry
Drug Trials
Bactrim DS 800Mg-160Mg Tablet 1
Akkermansia muciniphila 1
[PRP] platelet rich plasma 1
Probiotic 1
Silicone Gel 1

These are the names sponsors entered on ClinicalTrials.gov that we have not matched to a single molecule. Some are drugs under a brand or code name; others are procedures, doses or arm labels.

Which publications cover Congenital Microtia? (20)

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

Publications
Publication Journal Year Major topic
Anxiety, Depression, Stress, and Self-Esteem in Turkish Parents of Children with Microtia. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association 2024 Yes
Our Evolution of Approaches to Microtia Reconstruction. Facial plastic surgery clinics of North America 2024 Yes
A Two-Stage Method for Adult Congenital Microtia: The Essentials of 15-Year Experience. The Laryngoscope 2023 Yes
Secondary ear reconstruction based on the Nagata method after unsatisfactory microtia surgery outcomes. Journal of plastic, reconstructive & aesthetic surgery : JPRAS 2023 Yes
Secondary surgery for the unsatisfactory auricle after auricular reconstruction. International journal of pediatric otorhinolaryngology 2022 Yes

Prevalence (51)

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
Microtia Prevalence at birth 1-5 / 10 000 United States US Exact
Microtia Point prevalence 1-5 / 10 000 United States US Unspecified
Microtia Prevalence at birth 1-5 / 10 000 United States US Exact
Microtia Point prevalence 1-5 / 10 000 United States US Exact
Microtia Point prevalence 1-5 / 10 000 United States US Exact

Rare-disease identity (2)

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

Rare-disease identity
Orphanet disease ORPHA code Relation Source
Microtia 83463 Exact Orphanet Rare Disease Ontology (ORDO)
Microtia 83463 Exact Orphadata Science knowledge files, Product 1

Not on this page

Not measured: delivery record.

Checked, with nothing recorded for this condition: serious adverse events in this condition's trials and sub-conditions in mesh.

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