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THE EFFICACY OF RESORBABLE PLATES VERSUS TITANIUM PLATES IN TERMS OF STABILITY IN MANDIBULAR FRACTURES.

Primary Purpose

Comparison of Resorbable Plates With Titanium Plates

Status
Recruiting
Phase
Not Applicable
Locations
Pakistan
Study Type
Interventional
Intervention
surgically mandible will be exposed to reduced the fracture anatomically and then fixated with either resorbable or the titanium plates
Sponsored by
Dow University of Health Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Comparison of Resorbable Plates With Titanium Plates focused on measuring Resorbable plates,titanium plates,stability

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • • Age group-18 years and above

    • Symphysis and body fractures.
    • Non-infected fracture site

Exclusion Criteria:

  • • Condylar fracture

    • Comminuted fractures
    • Patients with systemic bone diseases
    • Gunshot wounds
    • Pan-facial trauma
    • Infected wounds

Sites / Locations

  • Dow University of Health SciencesRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

resorbable plates, test group

titatnium plates, control group

Arm Description

after a surgical procedure under general anesthesia , resorbable plates will be placed on the fracture site of the mandibule in 20 patients out of 40 total sample size and will be compared with the titanium plates in the control group

after a surgical procedure under general anesthesia , titanium plates will be placed on the fracturte site in the mandible in 20 patients out of 40 total sample size and will be compared to the test group containing resorbable plates

Outcomes

Primary Outcome Measures

bone union
union of the fractured bone will be observed radiographically at the end of the first ,second and the third month by a cone beam computed tomography.

Secondary Outcome Measures

Full Information

First Posted
September 16, 2022
Last Updated
September 16, 2022
Sponsor
Dow University of Health Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT05547763
Brief Title
THE EFFICACY OF RESORBABLE PLATES VERSUS TITANIUM PLATES IN TERMS OF STABILITY IN MANDIBULAR FRACTURES.
Official Title
THE EFFICACY OF RESORBABLE PLATES VERSUS TITANIUM PLATES IN TERMS OF STABILITY AMONG PATIENTS WITH MANDIBULAR FRACTURES: A RANDOMIZED CONTROLLED TRIAL.
Study Type
Interventional

2. Study Status

Record Verification Date
September 2022
Overall Recruitment Status
Recruiting
Study Start Date
November 27, 2019 (Actual)
Primary Completion Date
November 9, 2022 (Anticipated)
Study Completion Date
November 9, 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Dow University of Health Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Objective To compare the efficacy of resorbable plates against titanium plates to determine the fixation stability in reducing mandibular fractures Method: Subjects will be recruited and divided into two groups by random allocation. Consents will be obtained and fracture sites will be examined clinically and radiographically. Control group will receive titanium plates and test group will receive resorbable plates. The patients will be recalled immediately at first postop day then at the end of the first month , second month and the third month.They will be evaluated for the reduction of the fractures.
Detailed Description
Study design: randomized controlled trial Study Setting: The study will be carried out at the Department Of Oral and maxillofacial Surgery in Dow University of Health Sciences and Civil Hospital Karachi Study Population: Samples will be recruited by setting the following criteria: Inclusion Criteria: Age group-18 years and above Symphysis and body fractures. Non-infected fracture site Exclusion Criteria: Condylar fracture Comminuted fractures Patients with systemic bone diseases Gunshot wounds Pan-facial trauma Infected wounds Sample Size: Total 40 patients will be carried out (20 in treatment & 20 in control group). Using PASS version 11, two sample proportions with 95% confidence interval, 90% power of the test, 100% proportion of union of the fracture in resorbable fixation (treatment group) and 99% in titanium (control group),calculated sample size is 35 in each group keeping the population at approximately 120 patients in six months, calculated sample size is 70 patients.(18) But due to the budget constraints treatment group (resorbable fixation) will contain 20 patients and control group (titanium) will contain 20 patients Sampling Technique: Consecutive Sampling Data Collection Procedure: Data will be collected from the patients after receiving informed consent. Baseline demographic variable will be recorded using a predesigned questionnaire. Patients will be allocated to either resorbable or titanium plate group through random allocation [through lottery method]. Assessment will be done clinically and radiographically on CBCT scan (available at Dow International Dental College) First follow up assessment will be done immediately post op. Further assessments will be done at the completion of 2nd month and and then the 3rd month. Statistical Analyses: Data will be entered and analyzed using SPSS v 22. Mean and standard deviation will be calculated for all continuous variables, whereas frequencies and percentages will be calculated for all categorical variables. Efficacy of the intervention group will be assessed using chi-squared test. Study Variables Independent Variables: Interventions: Titanium or Resorbable plates Dependent Variables Fixation stability Co-variates: Age, Gender, Fracture site

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Comparison of Resorbable Plates With Titanium Plates
Keywords
Resorbable plates,titanium plates,stability

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
resorbable plates, test group
Arm Type
Experimental
Arm Description
after a surgical procedure under general anesthesia , resorbable plates will be placed on the fracture site of the mandibule in 20 patients out of 40 total sample size and will be compared with the titanium plates in the control group
Arm Title
titatnium plates, control group
Arm Type
Experimental
Arm Description
after a surgical procedure under general anesthesia , titanium plates will be placed on the fracturte site in the mandible in 20 patients out of 40 total sample size and will be compared to the test group containing resorbable plates
Intervention Type
Procedure
Intervention Name(s)
surgically mandible will be exposed to reduced the fracture anatomically and then fixated with either resorbable or the titanium plates
Intervention Description
under general anesthesia , fracture site of the mandible will be exposed and fracture will be reduced anatomically and held together by either resorbable or titanium plates and then the incsion site will be closed with vicryl sutures and patient will be observed on the follow ups clinically and radiographically for the fracture reduction and stability of the fractures with resorbable plates as compared to the titanium plates.
Primary Outcome Measure Information:
Title
bone union
Description
union of the fractured bone will be observed radiographically at the end of the first ,second and the third month by a cone beam computed tomography.
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: • Age group-18 years and above Symphysis and body fractures. Non-infected fracture site Exclusion Criteria: • Condylar fracture Comminuted fractures Patients with systemic bone diseases Gunshot wounds Pan-facial trauma Infected wounds
Facility Information:
Facility Name
Dow University of Health Sciences
City
Karachi
State/Province
Sindh
ZIP/Postal Code
74200
Country
Pakistan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dr.Shaheen Ahmed, FCPS
Phone
+923212275892
Email
drshaheenahm@gmail.com
First Name & Middle Initial & Last Name & Degree
Dr.Abdul Hafeez Shaikh, FCPS
Phone
+923332247325
Email
drabdulhafeezshaikh@hotmail.com

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

THE EFFICACY OF RESORBABLE PLATES VERSUS TITANIUM PLATES IN TERMS OF STABILITY IN MANDIBULAR FRACTURES.

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