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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03887234
Other study ID # R18114
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date September 1, 2018
Est. completion date October 19, 2022

Study information

Verified date December 2022
Source University of Turku
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study follows early wound healing using knot hiding titanium implants in coracoclavicular ligament reconstruction. A further aim is to compare two techniques where the semitendinosus tendon graft either runs through the coracoid drill hole or goes around the coracoid.


Description:

A modified arthroscopic technique for coracoclavicular ligament reconstruction was used based on a previous technique where the supportive device and the semi tendon graft share the clavicular and coracoid drill holes. A notable problem with the previous technique was large protruding suture knots on the washer and clavicle, which could predispose to wound infection. In this new modified technique, new implants were introduced. The new implant hides the suture knot and less foreign material is needed. The purpose of this study is to follow the patients operated using the new implants with special attention to early clavicular wound healing. A further aim is to compare a technique where the semitendinosus graft runs through clavicular and coracoid drill holes versus a technique where the graft runs under the coracoid process.


Recruitment information / eligibility

Status Completed
Enrollment 27
Est. completion date October 19, 2022
Est. primary completion date October 19, 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 16 Years to 70 Years
Eligibility Inclusion Criteria: Clinical diagnosis of chronic acromioclavicular luxation Exclusion Criteria: Severe new trauma after the treatment

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Coracoclavicular ligament reconstruction
Arthroscopically conducted ligament reconstruction for the treatment of an AC dislocation

Locations

Country Name City State
Finland Paavo Nurmi Centre, University of Turku Turku

Sponsors (1)

Lead Sponsor Collaborator
University of Turku

Country where clinical trial is conducted

Finland, 

Outcome

Type Measure Description Time frame Safety issue
Primary Total number of wound infections in the clavicular describing the safety of the used implant Clinical sign questionnaire, scale 0-1 (no-yes) two months
Secondary Constant score, scale 0-100, 100 denoting excellent General shoulder test; describes the general state of the shoulder Score is taken postoperatively and after two years follow-up
Secondary Simple shoulder test, scale 0-12, 12 denoting excellent General shoulder test; describes the general state of the shoulder Score is taken postoperatively and after two years follow-up
Secondary Nottingham clavicle score, scale 20-100, 100 denoting excellent AC joint specific test; describes the state of the AC joint and clavicle Score is taken postoperatively and after two years follow-up
Secondary Clavicular tunnel diameter Describes possible adverse expansion of the tunnel; millimeters The measure is taken postoperatively and after two years follow-up
Secondary Coracoclavicular distance Describes possible adverse increase of the coracoclavicular distance; millimeters The measure is taken postoperatively and after two years follow-up
See also
  Status Clinical Trial Phase
Completed NCT01205763 - Evaluation of Effects of Clavicular Hook Plate on Subacromial Space N/A