Postoperative Pain After Ambulatory Arthroscopic Shoulder Surgery
NCT ID: NCT02924519
Last Updated: 2016-10-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
150 participants
OBSERVATIONAL
2014-05-31
2018-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Of particular interest is prediction of postoperative pain after outpatient arthroscopic shoulder surgery since the clinical experience is that surgery does not always provides pain relief and the interindividual variation in acute postoperative pain intensity is significant. In addition, a Swedish study has shown that shoulder operations are associated with longer convalescence than other orthopaedic outpatient surgeries.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Chronic Pain After Shoulder Arthroplasty
NCT01900223
Post-operative Pain After Shoulder Surgery
NCT03732456
From ACute To Chronic Postoperative Shoulder Pain in Patients for Elective Lobectomy
NCT01552746
Natural History of Pain After Shoulder Arthroplasty Conducted With Multimodal Analgesia
NCT03021096
Which Factors Influence the Outcome After Anatomical and Reverse Shoulder Arthroplasty?
NCT04258267
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
* Preoperative shoulder pain (type, intensity and duration)
* Preoperative pain in other areas besides the shoulder
* Brief Pain Inventory (BPI)
* Western Ontario Rotator Cuff Index (WORC)
* Single Assessment Numeric Evaluation (SANE)
* 3 validated physiological questionnaires:
* State Trait Anxiety (STAI)
* Pain Catastrophizing Scale (PCS)
* Hospital Anxiety and Depression Scale (HADS)
In addition a cold pressor test is performed on the day of surgery to test the patients' threshold and ability to repress pain.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* mental disorders
* Unable to speak and/or read Danish
* Shoulder surgery within the last year
* Raynauds phenomenon
* Cuff suture
* Biceps tenodesis
* Labrum suture
18 Years
110 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Regionshospitalet Horsens
OTHER
University of Aarhus
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
1-10-72-103-14
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.