Comparative Study Evaluating Stability of Fracture Segments After Treatment of Mandibular Angle Fracture With 3d Strut Plate With or Without IMMF.

Sponsor
Cairo University (Other)
Overall Status
Unknown status
CT.gov ID
NCT03640039
Collaborator
(none)
16
2
16.7

Study Details

Study Description

Brief Summary

comparative study evaluating stability of fracture segments in mandibular angle fracture with 3d strut plate with or with out post operative IMMF.

Condition or Disease Intervention/Treatment Phase
  • Procedure: 3d strut plate.
N/A

Detailed Description

Two group of patient with mandibular angle fracture indicated for open reduction and internal fixation ,first group will be fixed with 3d stut plate with post operative IMMF. Second group will be fixed with 3d strut plate with out post operative IMMF.

Eligble patients will be randomised in equal proportions between study group (3d strut plate with out post operative IMMF) and control group (3d strut plate with post operative IMMF).

A- 3D strut plate without post operative IMMF:
  • Pre operative computed tomography will be done for patient.

  • Intra operative :all cases will under go general anathesia.

  • Exposure of the fracture segments using vestubular incision.

  • Inter-maxillary fixation will be done.

  • The fracture segment will be reduced in normal anatomic postion guided with occlusion.

  • The fracture segment will be fixed in postion using 3d srut plate.

  • Closure of surgical incision.

  • Post operative computed tomograghy will be done for the patient.

  • Patient will be dismissed from operation room without IMMF.

B- 3D strut with post operative IMMF:
  • Pre operative computed tomography will be done for patient.

  • Intra operative :all cases will under go general anathesia.

  • Exposure of the fracture segments using vestubular incision.

  • Inter-maxillary fixation will be done.

  • The fracture segment will be reduced in normal anatomic postion guided with occlusion.

  • The fracture segment will be fixed in postion using 3d srut plate.

  • Closure of surgical incision.

  • Post operative computed tomograghy will be done for the patient.

  • Patient will be dismissed from operation room with IMMF for 15 days.

Follow up for both groups :

Clinical examination will be done at first week post operative and patients will be examined every week for one month. Last follow up visit will be after three months post operative.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
16 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
A Radomized clinical trial. Parallel group study. A trial will be carried out in hospital of oral and maxillofacial surgery department - faculty of dentistry cairo university. Equal randomization: participants with equal probabilities for intervention. Positive controlled: both groups receiving treatment.A Radomized clinical trial. Parallel group study. A trial will be carried out in hospital of oral and maxillofacial surgery department - faculty of dentistry cairo university. Equal randomization: participants with equal probabilities for intervention. Positive controlled: both groups receiving treatment.
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Comparative Study Evaluating Stability of Fracture Segments After Treatment of Mandibular Angle Fracture With 3d Strut Plate in Two Groups One With IMMF and Anthor Without IMMF ;Randomized Clinical Trial.
Anticipated Study Start Date :
Jan 11, 2019
Anticipated Primary Completion Date :
Mar 1, 2020
Anticipated Study Completion Date :
Jun 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: study group: 3d strut plate fixation without post op IMMF.

Open reduction and internal fixation with 3d strut plate without post operative IMMF.

Procedure: 3d strut plate.
Under general anathesia fracture will be exposed and fixed with 3d srut plate.Wound closed in standered fashion. patient will be released from operating room with out IMMF.

Active Comparator: control group: 3d srut plate fixation with post op IMMF.

Open reduction and internal fixation with 3d strut plate with post operative IMMF for 15 days.

Procedure: 3d strut plate.
Under general anathesia fracture will be exposed and fixed with 3d srut plate.Wound closed in standered fashion. patient will be released from operating room with out IMMF.

Outcome Measures

Primary Outcome Measures

  1. stability of fracture segments. [15 days post operative.]

    post operative bimanual manipulation of the fracture segment.

Secondary Outcome Measures

  1. inferior alveolar nerve injury. [pre operative and 1 week post operative.]

    measurment by:Neurosensory testing: patient will be asked if there was numbness without stimulus and on stroking the lower lip skin with afinger.The patient will be asked to grade the sensation present on an analog scale from 0 (no sensation) to 10 (completely normal sensation)

  2. Accuracy of fracture reduction. [one week post operative.]

    Post operative. Through computed tomography by measuring inter ramus distance using lingula as reference to measure.

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years to 60 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Patients with mandibular angle fracture with or witout other fracture indicated for Open reduction internal fixation in the mandible.

  • Patient over 15 years old age and both sexes were included in this study.

  • Patients should be free from any systemic disease that may affect normal healing of bone, and predictable outcome.

  • Patients with good general condition allowing major surgical procedure under general anesthesia.

  • Patients with physical and psychological tolerance.

Exclusion Criteria:
  • Patients with comminuted fractures as it is not indicated for compression osteosynthesis like3d strut plate .

  • Patients with high risk systemic diseases like uncontrolled diabetes mellitus. As uncontrolled diabetes mellitus has a negative impact on normal bone healing.

  • Patients with old and/or mal-union fractures. As they will affect accuracy of reduction of the fractured segments.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Cairo University

Investigators

  • Study Director: Hesham A Hakam, Prof, Cairo University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Mohamed Khater tarek, Assistant lecturer., Cairo University
ClinicalTrials.gov Identifier:
NCT03640039
Other Study ID Numbers:
  • 2972018
First Posted:
Aug 21, 2018
Last Update Posted:
Aug 21, 2018
Last Verified:
Aug 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Mohamed Khater tarek, Assistant lecturer., Cairo University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 21, 2018