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Postoperative Pain After Ambulatory Arthroscopic Shoulder Surgery

Postoperative Pain After Ambulatory Arthroscopic Shoulder Surgery

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02924519
Enrollment
150
Registered
2016-10-05
Start date
2014-05-31
Completion date
2018-10-31
Last updated
2016-10-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Postoperative Pain

Brief summary

Shoulder disorders are frequent, often associated with pain and occur in 7-34% of the general population and in 21% of the elderly population. 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.

Detailed description

This study is a prospective cohort with 6 months follow-up. Patients receive 5 questionnaires (preoperatively, 24 hours, 1 week, 3 months, 6 months, 1 and 2 years after surgery). The questionnaires contain questions about: * 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.

Interventions

None listed

Sponsors

Regionshospitalet Horsens
CollaboratorOTHER
University of Aarhus
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 110 Years
Healthy volunteers
No

Inclusion criteria

* Arthroscopic shoulder surgery (subacromial decompression and acromioclavicular joint resection).

Exclusion criteria

* • \< 18 years * mental disorders * Unable to speak and/or read Danish * Shoulder surgery within the last year * Raynauds phenomenon * Cuff suture * Biceps tenodesis * Labrum suture

Design outcomes

Primary

MeasureTime frameDescription
Chronic postoperative pain6 months after surgeryMeasured on a numerical rating scale (NRS; 0=no pain and 10=worst possible pain. Chronic postoperative pain is defined as NRS\>=3 with an impact on daily living
Acute postoperative pain24 hours after surgeryMeasured on a numerical rating scale (NRS; 0=no pain and 10=worst possible pain. NRS\>3= acute postoperative pain

Secondary

MeasureTime frameDescription
Acute postoperative pain1 week after surgeryMeasured on a numerical rating scale (NRS; 0=no pain and 10=worst possible pain. NRS\>3= acute postoperative pain
Preoperative psychological predictors for chronic pain6 months after surgeryHospital Anxiety and Depression Scale (HADS)
Preoperative physical predictors for chronic pain6 months after surgeryCold pressure test
Preoperative comorbidity6 months after surgeryOther places than the shoulder

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026