Effect of cinopar in mandibular fracture

Phase 3

Recruiting

• Conditions: Mandibular bone fracture.; Fracture of mandible, unspecified; S02.60

• Registration Number: IRCT20180507039576N1
• Lead Sponsor: Yazd University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 21 June 2021

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

18-60 year
Mandibular fracture
Open reduction and internal fixation

Exclusion Criteria

Infection
Patient with a history of fracture
Patient taking immunosuppressive, corticosteroid and digoxin
The level of calcium greater than 10

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Bone healing. Timepoint: Before surgery and one month after surgery. Method of measurement: Evaluated both qualitatively, based on subjective fracture line changes , and quantitatively based on Hounsfield unit .

Secondary Outcome Measures

Name	Time	Method
Pain. Timepoint: 7, 14, 21, 28 days after surgery. Method of measurement: Visual Analogue Scale.;Swelling. Timepoint: 7, 14, 21, 28 days after surgery. Method of measurement: Examination.;Ecchymosis. Timepoint: 7, 14, 21, 28 days after surgery. Method of measurement: Examination.;Pus discharge. Timepoint: 7, 14, 21, 28 days after surgery. Method of measurement: Examination.;Dehiscence. Timepoint: 7, 14, 21, 28 days after surgery. Method of measurement: Examination.