Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02510339
Other study ID # 15.047.04
Secondary ID
Status Completed
Phase N/A
First received July 8, 2015
Last updated April 7, 2017
Start date January 10, 2016
Est. completion date March 1, 2017

Study information

Verified date October 2015
Source Orlando Health, Inc.
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The goal of this project is to determine the incidence of intra-articular knee pathology following tibial shaft fractures as evaluated by intraoperative knee aspiration and physical exam, and to evaluate for chondral injuries following treatment with a suprapatellar tibial nail via MRI.


Description:

Suprapatellar tibial nailing is gaining popularity throughout the orthopedic community for tibial shaft fractures, however the secondary effects of this technique on the articular cartilage of the knee is unknown. Additionally, the incidence of intra-articular knee pathology in the face of tibial shaft fractures has not been described in the orthopedic literature. An undiagnosed cruciate/collateral ligament injury can result in post-traumatic arthritis, as well as a delay in justified ligamentous reconstruction of the knee, causing further injury. Long term sequelae of now commonplace suprapatellar nailing on the patellofemoral joint of the knee have been sparsely elucidated in the literature.

The primary objective is to determine the consequences of suprapatellar tibial nailing on cartilage of the patellofemoral joint.

As a secondary objective, this study will seek to determine the incidence of intra-articular knee pathology following tibial shaft fractures in patients presenting to Orlando Regional Medical Center.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date March 1, 2017
Est. primary completion date March 1, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

1. skeletally mature

2. open or closed fractures of the tibial shaft

Exclusion Criteria:

1. concomitant tibial plateau or tibial pilon injuries

2. a knee dislocation

3. skeletally immature

4. those who will undergo standard (infra-patellar) tibial nailing

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Observation
Administration of two questionnairs during post operative visits.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Orlando Health, Inc.

Outcome

Type Measure Description Time frame Safety issue
Primary Consequences of suprapatellar tibial nailing During follow up visits, subjects will be given the Olerud-Molander questionnaire to complete. The data from that form will be analyzed for each visit. One year
Secondary Incidences of intra-articular knee pathology Post-operative radiographs will be analyzed during each visit per standard of care. One year.
Secondary Functional assessment The functional assessment/progress of the patient will be noted at each follow up visit. One year
See also
  Status Clinical Trial Phase
Completed NCT02728362 - Suprapatellar Nailing of Tibial Shaft Fractures