Microtia

4

Review clinical trials related to Microtia. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Evaluation of the Auryzon™ EAR 2.0 System in Ear Reconstruction

This study aims to improve surgical outcomes for children and young adults with ear differences severe secondary to congenital conditions (like microtia, a condition where the ear is underdeveloped), trauma (such as dog bites), or surgical resections secondary to skin cancer. The investigators have developed a novel medical device to shape cartilage into pre-determined shapes that, once assembled, assists the surgeon in creating an anatomically accurate cartilaginous ear framework, reduce surgery time, and minimize wire need. Other factors that might affect the quality of surgical outcomes will be examined in clinical trial participants.

Participants needed: 30
Trial details
Age: 5-20Biological sex: AllType: InterventionalSponsor: Nemours Children's ClinicUpdated: Dec 29, 2025Locations: 1
Eligibility criteria

Patients aged 5-20 years seeking to undergo surgical ear reconstruction or micro... [+4]

Patients who will be ≤4 years old, or ≥21 years old at time of surgery [+5]

Status: Recruiting

InterNatIonal CHildhood Leukemia Microbiome/MEtabolome Cohort

Nutritional status is a measurable and modifiable factor that is often not considered during treatment and its clinical impact undervalued due in part to the heavy demands on clinicians in low and middle income countries to deliver therapy to large numbers of patients. The proposed study will create a biobank of clinical data and biological specimens which will foster future studies on cancer progression and prognosis as well as toxicities during treatment which may impact survivorship and late-effects. Eligible patients must be between 3 years and 18 years of age at time of assent/consent, have newly diagnosed B- or T-cell acute lymphoblastic leukemia or mixed phenotype acute leukemia confirmed by pathology report, and must be receiving treatment at one of the participating centers. Patients receiving hematopoietic cell transplant will be excluded. Institutions were selected to ensure representation of several global health indicators related to nutritional status and wealth classification according to the World Bank. Data related to demographic variables (socioeconomic status, food security), lifestyle habits (diet, physical activity), nutritional anthropometrics (height, weight and arm anthropometry), and nutritional biological indices (stool and blood) will be collected at designated timepoints throughout treatment and one year after the end of treatment.

Participants needed: 4,900
Trial details
Age: 3-18Biological sex: AllType: ObservationalSponsor: Columbia UniversityUpdated: Jul 22, 2025Locations: 8
Eligibility criteria

Patients must be between 3 years and 18 years of age at time of assent/consent. [+2]

Status: Recruiting

Microbiome Metabolites and Alcohol in HIV to Reduce CVD RCT

Among people living with HIV, heavy drinking increases the risk of heart disease and death. Studies suggest that alcohol changes the number and kind of bacteria in your gut and these changes increase the risk of heart disease and death. This randomized controlled trial will determine whether a pill containing healthy gut bacteria can increase the number good bacteria in the gut, lower levels of inflammation, and lower the risk of heart disease and death.

Participants needed: 250
Trial details
Phase: Phase 2Age: 18-89Biological sex: AllType: InterventionalSponsor: Vanderbilt University Medical CenterUpdated: Jun 24, 2025Locations: 1
Eligibility criteria

HIV infected

Not fluent in English

Status: Not yet recruiting

Safety and Efficacy of Connecting the Residual Ear to the Cartilage Scaffold in First- vs. Second-Stage Surgery

Eligible patients will be admitted from the outpatient clinic to complete the relevant examinations after admission(Preoperative routine examination and chest CT). The baseline parameters will be registered when admitted to hospital, including case number, diagnosis, sex, age, height, weight, and underlying medical conditions. Patients have at least 12 hours to consider participation in the study and will be given the opportunity to ask questions about the study. Written informed consent will be obtained by the surgical resident or the surgeon after admission to the hospital. Randomization will be done by relevant member . After inclusion, patients will be allocated to one of the two study groups (First-stage Connection or Second-stage Connection) using an online randomization program. The perioperative care will be the same for all included patients.Surgery will be performed by experienced surgeons, with non-expanded ear reconstruction using autologous rib cartilage. The surgery normally comprises two stages. After each surgery, details and duration of the surgery will be documented. For each stage of surgery, patients are scheduled for visits about 3-6 months. In addition, after the total surgery, patients are to fill out 'Glasgow Benefit Inventory' and 'Patient and Observer Scar Assessment Scale'.

Participants needed: 78
Trial details
Age: 6-30Biological sex: AllType: InterventionalSponsor: Sichuan Provincial People's HospitalUpdated: May 16, 2025Locations: 1
Eligibility criteria

Patients were fully informed about the purpose, modalities and risks associated... [+1]

Patients combined with other ear diseases such as ear fistula, titis media, etc. [+2]