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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT04041258
Other study ID # CLAPS
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date July 30, 2019
Est. completion date May 1, 2021

Study information

Verified date August 2021
Source Istituto Ortopedico Rizzoli
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is an interventional study for clinical and radiographic evaluation of patients operated for pseudoarthrosis of the clavicle


Description:

The aim of our study is to collect clinical and radiographic data from patients operated for pseudoarthrosis of the clavicle from 2007 to 2017 at the Rizzoli Orthopedic Institute, in order to evaluate the clinical and radiographic results of the treatment. This is an interventional study and patients will be contacted by telephone to verify their willingness to perform a visit (including a bilateral radiographic) at the Rizzoli Orthopedic Institute


Recruitment information / eligibility

Status Terminated
Enrollment 20
Est. completion date May 1, 2021
Est. primary completion date July 30, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years to 65 Years
Eligibility Inclusion Criteria: 1. 18-65 years of pseudarthrosis intervention 2. Males and Females 3. Patients treated for pseudoarthrosis of the clavicle between 2007 and 2017 at the Rizzoli Orthopedic Institute Exclusion Criteria: 1. Floating shoulder 2. subjects who present contraindications to radiographic examination at the time of telephone contact

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
pseudoarthrosis of clavicle
Pseudoarthrosis represents a complication following a fracture, resulting in persistent symptoms and functional limitation, which prolongs the recovery time for the patient and necessitates new surgery. The purpose of surgery for pseudoarthrosis is to re-establish the length and alignment of the clavicle in an environment favorable to the union of bone fragments.

Locations

Country Name City State
Italy Rizzoli Orthopaedic Institute Bologna

Sponsors (1)

Lead Sponsor Collaborator
Istituto Ortopedico Rizzoli

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary range of motion ROM improvement of range of motion measure (in grade) at least 1 year of follow up
Primary presence of dyskinesias objective clinical evaluation (elevation, external rotation, abduction) with constant scale (0-25 points) at least 1 year of follow up
Primary alteration of the clavicle length measure (mm) obtained from radiographic evaluation at least 1 year of follow up
Secondary evaluate shoulder function improvement in Assessment Shoulder and Elbow Scale (ASES) (0-100 points) at least 1 year of follow up