Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02850861
Other study ID # WCH-01
Secondary ID
Status Completed
Phase N/A
First received July 6, 2016
Last updated July 29, 2016
Start date January 2014
Est. completion date June 2016

Study information

Verified date July 2016
Source West China Hospital
Contact n/a
Is FDA regulated No
Health authority China: National Natrural Science Foundation
Study type Interventional

Clinical Trial Summary

In condylar fracture surgery, reduction is the most difficult step and the key factor which determined the postoperative outcome. Therefore, the aim of this study is to develop a new instrument, which the investigators call condylar redactor, to assist the surgeon to reduct the condylar segments effectively.


Description:

In this prospective cohort study, it involved condylar fractures patients who were received surgical treatment from January 2014 to June 2016. Patients in the experimental group were treated with the condylar reductor, and patients in the control group were treated with the traditional surgical instruments. The primary outcome variable was reduction time and reduction rate. The continuity correction X2 and test student t test were used.


Recruitment information / eligibility

Status Completed
Enrollment 2
Est. completion date June 2016
Est. primary completion date January 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- patients aged 18-60 with mandibular condylar fractures were treated in Oral and maxillofacial surgery department, West China hospital of stomatology, China from January 2014 to January 2016.

Exclusion Criteria:

- patients refused to participate in the clinical trial;

- condylar fracture dislocation was not obvious, conservative treatment can be used;

- mandibular condylar comminuted fracture;

- mandibular condyle need to be reconstructed.

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Condylar reductor
A new surgical instrument was designed to assist the surgeons to perform condylar fracture reduction.

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Junhui Cui West China Hospital

Outcome

Type Measure Description Time frame Safety issue
Primary intraoperative reduction time intraoperative Yes