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OpenTrials
Completed

NCT Number: NCT01900223

Chronic Pain After Shoulder Arthroplasty

Chronic pain is relatively common after different types of surgery. The investigators intend to study prevalence, characteristics and risk factors of chronic pain after shoulder arthroplasty, focusing on neuropathic pain characteristics, and risk factors such as preoperative pain, severe acute postoperative pain, age, gender, and pain elsewhere.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients operated with any shoulder prosthesis between april 2011 and april 2012 in Denmark

Exclusion criteria

  • Secondary prosthesis
  • Bilateral prosthesis
  • Age below 18
  • Reoperated in the same shoulder after the prosthesis

Treatment and study plan

Primary outcomes

  1. Current pain intensity

    Time frame: At time of completing the questionnaire, which is sent to patients 1-2 years after their shoulderprosthesis.

    Pain score by Numeric Rating Scale 0-10

Secondary outcomes

  1. preoperative pain intensity

    Time frame: recalled

    Pain intensity by Likert scale

Sponsors and collaborators

Lead sponsor

Karen Bjørnholdt

Other

Collaborators

  • Augustinus Fonden
  • Central Denmark Region
  • Horsens Hospital

Registry information

Official study title

Chronic Pain After Shoulder Arthroplasty: Epidemiology and Risk Factors.

Important dates

Study start
2013
Primary completion
2013
Study completion
2013
First posted
Jul 16, 2013
Registry last updated
Jan 14, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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