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Reconstruction Of Acute Coracoclavicular Ligament Disruption With and Without Tendon Graft

Not Applicable
Conditions
Acromioclavicular Joint Dislocation
Interventions
Procedure: tendon graft
Other: No intervention
Registration Number
NCT03060564
Lead Sponsor
Dr. Brian Lee
Brief Summary

To evaluate patient function, radiographic changes and complication rates of acute coracoclavicular (CC) joint reconstruction with and without the use of tendon graft as an augmentation to repair.

Detailed Description

Acromioclavicular (AC) joint dislocations comprise up to 12% of shoulder girdle injuries. Many methods of reconstructing the coracoclavicular ligaments, which provide vertical stability of the acromioclavicular joint, have been described. The use of tendon graft to augment the reconstruction provides improved biomechanical stability, less radiographic changes postoperatively including loss of reduction, and improved function. However, the use of a tendon graft necessitates larger drill holes in the clavicle when compared to suture-only repair constructs. The size and placement of these tunnels in the clavicle have been associated with a higher rate of complications.

It has been shown that repairs in the setting of acute injury demonstrate less complications including loss of reduction when compared with chronic dislocations. However, other reports describing repair of acute AC joint dislocations without graft augmentation have described significant changes in coracoclavicular distance with routine follow up radiographs, and up to 90% implant migration rates. While use of tendon graft would be expected to provide further stability, they may in turn cause an increased complication rate.

1. To determine complication rates in the reconstruction of AC joint dislocations with and without the use of tendon graft.

2. Determine patient satisfaction, the ASES, Constant, SF-12, SANE, SST scores of shoulders that undergo reconstruction of acute AC joint dislocations with and without the use of graft.

3. The investigation aims to determine whether or not graft should be used in the reconstruction of acute AC joint dislocations.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
150
Inclusion Criteria
  • Displaced acromioclavicular joint dislocation sustained within 3 weeks of surgery
  • recommended for operative fixation
  • age 18 years or older
Exclusion Criteria
  • Open dislocation
  • previous acromioclavicular surgery
  • unable to follow study protocol
  • concomitant injury requiring surgery (rotator cuff repair, biceps tenotomy/tenodesis)
  • active infection
  • unable to follow postoperative rehabilitation guidelines
  • reconstruction with coracoclavicular screw or hook plate.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
AC repair with tendon grafttendon graftacromioclavicular repair with tendon graft.
AC repair with no tendon graftNo interventionacromioclavicular repair without tendon graft/no intervention
Primary Outcome Measures
NameTimeMethod
Complication Rates with and without the use of graft tendons2 years

loss of radiographic reduction, infection, need for more surgery

(American Shoulder Elbow Society (ASES)2 years

Shoulder Function survey (17 multiple choice questions).

Simple Shoulder Test (SST)2 years

Shoulder Function survey (12 yes/no questions)

Visual Analog Score (VAS)2 years

Measurement of shoulder pain from 0 (no pain) to 10 (unbearable distress)

Single Assessment Numerical Evaluation (SANE)2 years

Patient assessment rating from 0-100 shoulder normality

Instability Index Constant Score (ISIS)2 years

Shoulder Instability survey for last 4 weeks (yes/no and multiple choice). Score is graded poor, fair, good, excellent.

Short Form-122 years

This survey assesses patient's health satisfaction. This information will help keep track of how patients feel and how well patients are able to do your usual activities. (12 multiple choice questions)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Cedars-Sinai Kerlan-Jobe Institute at White Memorial Hospital

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Los Angeles, California, United States

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