Clinical Trials Directory

Trials / Completed

CompletedNCT03335410

The Recuperation of Patients After Elective Shoulder Surgery Observational Cohort Study

The Recuperation of Patients After Elective Shoulder Surgery -a National Observational Cohort Study

Status
Completed
Phase
Study type
Observational
Enrollment
122 (actual)
Sponsor
Tampere University Hospital · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

Around 6400 shoulder surgeries are performed yearly in Finland. The procedure is mainly day-case surgery and the patients go home in the afternoon. Shoulder surgery is one of the most common procedures performed in private surgical practices. Because of the complex nature of the joint, the recovery may be complicated by severe opstoperative pain, which is relieved with strong opioids. Recently this has been addressed in the literature, as prescribed opioids too often lead to substance abuse. Pain in the acute phase after surgery is one of the common risk factors for persistent postoperative pain, which is a major burden for both the individual patient and the society. In this prospective, observational cohort study we aim to describe current standards of practice in planning and taking care of anaeshtesia and prescribing opioids and adjuvants for postoperative pain relief at home.

Detailed description

Around 6400 shoulder surgeries are performed yearly in Finland. The procedure is mainly day-case surgery and the patients go home in the afternoon. Shoulder surgery is one of the most common procedures performed in private surgical practices. Because of the complex nature of the joint, the recovery may be complicated by severe opstoperative pain, which is relieved with strong opioids. Recently this has been addressed in the literature, as prescribed opioids too often lead to substance abuse. Pain in the acute phase after surgery is one of the common risk factors for persistent postoperative pain, which is a major burden for both the individual patient and the society. In this prospective, observational cohort study we aim to describe current standards of practice in planning and taking care of anaeshtesia and prescribing opioids and adjuvants for postoperative pain relief at home. The data is collected prospectively from the care provider and the patient in a webrobol questionnaire at three time points: the day of surgery (care provider), one week after surgery (patient) and three months after surgery (patient).

Conditions

Interventions

TypeNameDescription
OTHERNon- interventionalNon- interventional

Timeline

Start date
2017-09-15
Primary completion
2018-01-15
Completion
2018-01-15
First posted
2017-11-07
Last updated
2018-09-06

Locations

14 sites across 1 country: Finland

Source: ClinicalTrials.gov record NCT03335410. Inclusion in this directory is not an endorsement.