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From ACute To Chronic Postoperative Shoulder Pain in Patients for Elective Lobectomy

CompletedNCT01552746
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

Shoulder pain is a well known problem after thoracical surgery. The pathogenesis of the pain is uncertain, but mainly a mix of referred pain and mechanical strain to the shoulder. It is believed to last a few days. Persisting shoulder pain after thoracical surgery is a problem 1 year after surgery, but it is unknown if it is related to acute postoperative shoulder pain. The purpose of the study is to systematically describe postoperative shoulder pain after lobectomy and examine the time progress up to 1 year after surgery.

Study details

Official title
From Acute to Chronic Postoperative Shoulder Pain in Patients for Elective Lobectomy
Conditions
Sponsor
Odense University Hospital
Collaborators
Vejle Hospital
Start date
2012-01
Primary completion
2012-12
Sex
All
Age range
from 18 Years
Results posted
No results posted in this snapshot
Countries
Denmark
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Patients for elective lobectomy * 18 years or older at the day of the operation * Satisfactory abilities to speak and read danish Exclusion Criteria: * Previous Thoracical Surgery. * Patients with diseases in the nervous system. * Patients with preoperative shoulder pain, neuropathies or sensory disturbances in the arm or shoulder. * Patients who are reoperated in the thorax in the study period or any other body-region within the first 4 postoperative days.

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT01552746