Mandibular Fractures Clinical Trial
Official title:
Evaluation of Bone Reduction Forceps in Reducing Mandibular Fracture
Verified date | June 2020 |
Source | Alexandria University |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Different methods have been used in reducing mandibular fractures. Bone reduction forceps provides precise reduction and stabilize mandibular fracture segments.
Status | Active, not recruiting |
Enrollment | 10 |
Est. completion date | September 1, 2020 |
Est. primary completion date | August 18, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 20 Years to 45 Years |
Eligibility |
Inclusion criteria - Adult patients aged from 20 to 45 years will be included. - Patients suffered from recent and uninfected. - Patients with isolated mandibular fractures. Exclusion criteria - Medically compromised patients that will be not fit for surgery. - Edentulous patients. - Non-displaced - Comminuted fracture with bone loss - Old fracture, more than 3 weeks |
Country | Name | City | State |
---|---|---|---|
Egypt | Outpatient Clinic of Oral and Maxillofacial Surgery Department, Faculty of Dentistry, Alexandria University, Egypt | Alexandria | Azarita |
Lead Sponsor | Collaborator |
---|---|
Hams Hamed Abdelrahman |
Egypt,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in radiodensitometric measurements | cone-beam computerized tomograms (CBCT) used to analyze the mean bone density at the site of fracture | at 3rd, 6th months | |
Primary | change in maximal mouth opening | maximal interincisal opening between maxillary and mandibular central incisors. | 1 week, 2 weeks, 1 month, 6 weeks, and 3 months | |
Primary | change in occlusion | Any occlusal disturbance including open bite or improper tooth contact will be recorded | 1 week, 2 weeks, 1 month, 6 weeks, and 3 months | |
Primary | change in pain level | Pain: will be measured on Visual Analogue Scale (VAS). The patients will be asked to rate their postoperative pain on a 4-point scale (0= none, 1= slight, 2= moderate, 3- severe) | 1 week, 2 weeks, 1 month, 6 weeks, and 3 months |
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