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Chin advancement using polyethylene chin implants

EFFICACY OF POROUS HIGH-DENSITY POLYETHYLENE AS IMPLANTS FOR CHIN AUGMENTATION- A CLINICAL STUDY

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/09/036467
Enrollment
10
Registered
2021-09-14
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: K089- Disorder of teeth and supporting structures, unspecified

Interventions

Intervention1: POROUS HIGH-DENSITY POLYETHYLENE CHIN IMPLANT(BIOPOREâ?¢): After administration of local anesthesia, incision will be placed intra orally and access will be gained to the chin region. T

Sponsors

Sanjeev N
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1)Patients presenting with retrogenia, based on the criteria mentioned below, for which surgical intervention is necessary. 2)Patients in whom growth has been completed. 3)Patients with a stable occlusion.

Exclusion criteria

Exclusion criteria: 1)Subjects with any major systemic illness. 2)Patients with psychiatric problems. 3)Patient with systemic conditions affecting the bones and teeth. 4)Patients with congenital deformities or syndromes affecting bones and teeth. 5)Patients with true mandibular hypoplasia.

Design outcomes

Primary

MeasureTime frame
Lateral cephalograms (with barium line) will be traced for hard tissue assessment by COGS analysis and Arnett soft tissue analysis which includes Transverse Vertical Line (TVL) and will be compared with the pre-operative cephalograms to assess the changes following the procedure. Lateral cephalograms (with barium line) taken pre operatively and post operatively will be super imposed to assess the changes. Patient and clinicianâ??s perception will be assessed by asking them to compare the pre and post op photographs. Timepoint: 4 weeks 8 weeks 12 weeks

Secondary

MeasureTime frame
Infection, nerve damage or paraesthesia if any.Timepoint: 4 weeks 8 weeks 12 weeks

Countries

India

Contacts

Public ContactSanjeev N

RAJARAJESWARI DENTAL COLLEGE AND HOSPITAL

madhumati_dr@rediffmail.com9844116475

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026