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Clinical Trials/CTRI/2021/01/030845
CTRI/2021/01/030845
Not yet recruiting
未知

Comparative Evaluation of Efficacy of CAD-CAM Assisted Patient Specific Polyetheretherketone (Peek) Plate with 3D Delta Titanium Plate for the Fixation of Mandibular Subcondylar Fractures - A Prospective Randomized Controlled Trial - Polyetheretherketone (PEEK)

Datta Meghe Institute of Medical Sciences Deemed to be University0 sites0 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
Health Condition 1: M96- Intraoperative and postproceduralcomplications and disorders of musculoskeletal system, not elsewhere classified
Sponsor
Datta Meghe Institute of Medical Sciences Deemed to be University
Status
Not yet recruiting
Last Updated
4 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
4 years ago
Study Type
Interventional

Investigators

Sponsor
Datta Meghe Institute of Medical Sciences Deemed to be University

Eligibility Criteria

Inclusion Criteria

  • Cases of unilateral mandibular subcondylar fractures (mostly associated with symphysis / parasymphysis fracture).
  • Patients should be free from any systemic disease that may affect normal healing of bone, and predictable outcome.
  • Systemically healthy patients with ASA I/II grades.
  • Patients with good general condition allowing major surgical procedure under general anaesthesia.

Exclusion Criteria

  • Patients with trifocal fractures in mandible will be excluded from the study.
  • Patients with old fractures as they might affect accuracy of reduction of the fractured segments.
  • Patient with comminuted fracture in condylar region
  • Patients with bone loss or soft tissue loss at fracture site
  • Endocrinopathies affecting calcium metabolism, chronic smokers, post menopausal women.
  • Patients with mixed dentition and edentulous lower arch
  • Evidence of infections at fracture site (diagnosed clinically, not with culture)
  • Epileptic patients
  • Medically compromised patients not fit for surgery.
  • Patient not willing for surgical treatment.

Outcomes

Primary Outcomes

Not specified

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