Development of patient specific implants and evaluation of their patient outcomes

Development of patient specific implants for the reconstruction of maxillofacial defects and comparison of presurgical and postsurgical clinical outcomes: A clinical trial - NIL

Status

Recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/01/061045

Enrollment

Registered

2024-01-02

Start date

Unknown

Completion date

Unknown

Last updated

2024-01-22

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

Conditions

Health Condition 1: K069- Disorder of gingiva and edentulousalveolar ridge, unspecified

Interventions

Intervention1: Patient Specific Implant: Patient specific implants are designed to adapt to with high precision and accuracy to the site with defect. It is used for the reconstruction of maxillofacial

Eligibility

Inclusion criteria

Inclusion criteria: Patients undergoing reconstruction of maxillofacial defects

Exclusion criteria

Exclusion criteria: Cases with previously failed autografts, free flaps or patient specific implants. Patients who have undergone radiotherapy.

Design outcomes

Primary

Measure	Time frame
Patient acceptance using Four face Q questionnaireTimepoint: Preoperative 1 month Postoperative 3 months postoperative	—

Secondary

Measure	Time frame
Speech assessment Nutritional statusTimepoint: Preoperative 1 month postoperative 3 months postoperative	—

Countries

India

Contacts

Public ContactKathiravan Selvarasu

Saveetha Dental College and Hospitals

dr.kathiromfs@gmail.com9677202463

Outcome results

None listed

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