Development of patient specific implants and evaluation of their patient outcomes
Phase 2
- Conditions
- Health Condition 1: K069- Disorder of gingiva and edentulousalveolar ridge, unspecified
- Registration Number
- CTRI/2024/01/061045
- Lead Sponsor
- il
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients undergoing reconstruction of maxillofacial defects
Exclusion Criteria
Cases with previously failed autografts, free flaps or patient specific implants.
Patients who have undergone radiotherapy.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Patient acceptance using Four face Q questionnaireTimepoint: Preoperative <br/ ><br>1 month Postoperative <br/ ><br>3 months postoperative
- Secondary Outcome Measures
Name Time Method Speech assessment <br/ ><br>Nutritional statusTimepoint: Preoperative <br/ ><br>1 month postoperative <br/ ><br>3 months postoperative