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CompletedNCT05234385SCJ InfectionUpdated Jun 5, 2024

Functional Outcome Following Surgical Treatment of Patients With Sternoclavicular Joint Infection

An observational study in Sternoclavicular Joint Infection, sponsored by University Hospital, Basel, Switzerland. Completed at 1 site in Switzerland. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-06-05.

Sponsored by University Hospital, Basel, Switzerland · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
14
Ages
18 Years and older
Sex
All
01

Study summary

The Sternoclavicular joints (SCJ) represents an important factor in stability of shoulder joint. Its influence and its function is important for the functionality of the shoulder. SCJ infection is a rare condition and remains often mistreated and potentially life threatening.

This study is to assess the cases treated at the University Hospital Basel with a surgical approach of extended resection of the SCJ. One prospective follow-up visit inclusive one physical examination per patient will be performed to evaluate the long-term functional results of arm, shoulder, hand function with the QuickDASH questionnaire.

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Conditions studied

  • Sternoclavicular Joint Infection

Keywords

  • QuickDASH questionnaire
  • extended SCJ resection
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In context

Infections

6,687 studies on the registry are indexed under Infections; 807 are open to participants now.

This study's enrollment of 14 is below the median of 240 across 2,136 observational studies indexed under Infections.

Browse Infections studies →

Lead sponsor

University Hospital, Basel, Switzerland is the lead sponsor of 968 studies on the registry; 191 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Probability sample

Study population

Patients diagnosed with SCJ infection and surgical treatment of extended SCJ resection, treated at the Department of Thoracic Surgery at the University Hospital Basel between 31.05.2011 and 28.02.2022.

Inclusion criteria

  • Patient assigned and treated at the Department of Thoracic Surgery, University Hospital Basel (USB)
  • At hospital admission diagnosed with clinical characteristics of sternoclavicular joint infection
  • Surgical treatment of extended SCJ resection received
  • Signed written informed consent according to ICH-GCP regulations prior to initiation of any protocol-specific activities/procedure
  • Patients who died will be included if a signed USB general research consent is available

Exclusion criteria

Exclusion Criteria:

  • Isolated sternal or clavicular infection
  • Patients received other surgery than extended SCJ resection at USB thoracic surgery
  • Inability to follow procedures or insufficient knowledge of language (German/French) or inability to give consent
  • Patients who have clearly stated that they would not agree in providing their clinical data for scientific purposes
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
14 participants (actual)
Patient registry
No
06

What researchers measure

Primary outcomes

  1. QuickDASH score

    QuickDASH score of the mobility of the arm, shoulder, hand and its function by using the QuickDASH questionnaire. The QuickDASH is scored in two components: the disability/symptom section (11 items, scored 1-5) and the optional high performance sport/music or work modules (4 items, scored 1-5). A higher score indicates greater disability.

    Time frame: one time assessment at the prospective follow-up visit (timeframe of maximal 1 hour)

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Study locations

1 site
  • Department of Thoracic Surgery, University Hospital of Basel
    Basel, 4031, Switzerland
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References and documents

Publications

  • Vujic J, Hojski A, Dackam SVC, Bachmann H, Lardinois D. Functional Outcomes of Patients With Sternoclavicular Joint Infection After Extended Resection. Ann Thorac Surg Short Rep. 2024 Jan 19;2(2):193-196. doi: 10.1016/j.atssr.2023.12.015. eCollection 2024 Jun. PubMed 39790151 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 5, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05234385
Lead sponsor
University Hospital, Basel, Switzerland
Responsible party
Sponsor
First posted
Feb 10, 2022
Start date
Jan 2, 2022
Primary completion
Apr 21, 2022
Completion
Apr 21, 2022
Last update
Jun 5, 2024

Study contacts

Didier Lardinois, Prof. Dr. med.
study director · Department of Thoracic Surgery, University Hospital Basel

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2024. You cannot join it, but the record below documents what was studied.

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