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A Pilot Study To Evaluate The Artificial Replacements Relating To Jaw And Face Which Are Fabricated By The Combination Of Digital And Conventional Workflow

Evaluation of extraoral maxillofacial prosthesis fabricated using combination of Digital and conventional workflow.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/09/036953
Enrollment
5
Registered
2021-09-29
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: Z448- Encounter for fitting and adjustment of other external prosthetic devices

Interventions

Intervention1: 3D printed customized mold of Acrylonitrile butadiene styrene (ABS) fabricated using Fused Deposition Method (FDM): We will scan the maxillofacial defect using 3D scanner. After develo

Sponsors

Datta Meghe Institute of medical Sciences NEW GEN IEDC
Lead Sponsor
Datta Meghe Institute of Medical Sciences
Collaborator

Eligibility

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1.Defect size not bigger than 9 x 12 cm (3.5 x 4.5 inches) 2.Agrees to wear the given prosthesis minimum 6 hours everyday 3.In the age group of 20 -70 years

Exclusion criteria

Exclusion criteria: Exclusion criteria: Not Cognizant enough to answer questionnaires Patients who are not ready to come for follow ups

Design outcomes

Primary

MeasureTime frame
good retention of the prosthesis and esthetic improvementTimepoint: 1 month—

Secondary

MeasureTime frame
improved overall quality of lifeTimepoint: 6 months—

Countries

India

Contacts

Public ContactDrSweta Kale Pisulkar

Dutta Meghe Institute of Medical Sciences,

bagde.ashu@gmail.com9021201578

Outcome results

None listed

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